{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AO-A12A-01A-21D-A10Y-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218304,"End_Position":179218304,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"C","Tumor_Sample_Barcode":"TCGA-AR-A1AS-01A-11D-A12Q-09","HGVSc":"c.1634A>C","HGVSp":"p.Glu545Ala","HGVSp_Short":"p.E545A","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1791/9093","CDS_position":"1634/3207","Protein_position":"545/1068","Amino_acids":"E/A","Codons":"gAg/gCg"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199158,"End_Position":179199158,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"C","Tumor_Sample_Barcode":"TCGA-D8-A1JP-01A-11D-A13L-09","HGVSc":"c.333G>C","HGVSp":"p.Lys111Asn","HGVSp_Short":"p.K111N","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"490/9093","CDS_position":"333/3207","Protein_position":"111/1068","Amino_acids":"K/N","Codons":"aaG/aaC"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-LD-A74U-01A-13D-A33E-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
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{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-OL-A5S0-01A-11D-A28B-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-BH-A208-01A-11D-A159-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-A2-A0YK-01A-22D-A117-09","HGVSc":"c.3140A>T","HGVSp":"p.His1047Leu","HGVSp_Short":"p.H1047L","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/L","Codons":"cAt/cTt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-E9-A1N5-01A-11D-A14G-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
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{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-OL-A6VQ-01A-12D-A41F-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-E9-A1NH-01A-11D-A14G-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-E2-A1BD-01A-11D-A12Q-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199772,"End_Position":179199772,"Variant_Classification":"Silent","Reference_Allele":"C","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-AN-A046-01A-21W-A050-09","HGVSc":"c.435C>T","HGVSp":"p.=","HGVSp_Short":"p.N145N","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"synonymous_variant","cDNA_position":"592/9093","CDS_position":"435/3207","Protein_position":"145/1068","Amino_acids":"N","Codons":"aaC/aaT"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234219,"End_Position":179234219,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AN-A046-01A-21W-A050-09","HGVSc":"c.3062A>G","HGVSp":"p.Tyr1021Cys","HGVSp_Short":"p.Y1021C","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3219/9093","CDS_position":"3062/3207","Protein_position":"1021/1068","Amino_acids":"Y/C","Codons":"tAc/tGc"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-AR-A24O-01A-11D-A167-09","HGVSc":"c.3140A>T","HGVSp":"p.His1047Leu","HGVSp_Short":"p.H1047L","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/L","Codons":"cAt/cTt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AN-A0AJ-01A-11W-A019-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A2-A04W-01A-31D-A10Y-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-E2-A15C-01A-31D-A12B-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A2-A0T7-01A-21D-A099-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234286,"End_Position":179234286,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A2-A0T7-01A-21D-A099-09","HGVSc":"c.3129G>A","HGVSp":"p.Met1043Ile","HGVSp_Short":"p.M1043I","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3286/9093","CDS_position":"3129/3207","Protein_position":"1043/1068","Amino_acids":"M/I","Codons":"atG/atA"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218306,"End_Position":179218306,"Variant_Classification":"Missense_Mutation","Reference_Allele":"C","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AO-A0J7-01A-11W-A050-09","HGVSc":"c.1636C>A","HGVSp":"p.Gln546Lys","HGVSp_Short":"p.Q546K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1793/9093","CDS_position":"1636/3207","Protein_position":"546/1068","Amino_acids":"Q/K","Codons":"Cag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234275,"End_Position":179234275,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-C8-A278-01A-11D-A167-09","HGVSc":"c.3118A>G","HGVSp":"p.Met1040Val","HGVSp_Short":"p.M1040V","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3275/9093","CDS_position":"3118/3207","Protein_position":"1040/1068","Amino_acids":"M/V","Codons":"Atg/Gtg"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-C8-A278-01A-11D-A167-09","HGVSc":"c.3140A>T","HGVSp":"p.His1047Leu","HGVSp_Short":"p.H1047L","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/L","Codons":"cAt/cTt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-PE-A5DD-01A-12D-A27P-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199690,"End_Position":179199690,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A2-A04V-01A-21W-A050-09","HGVSc":"c.353G>A","HGVSp":"p.Gly118Asp","HGVSp_Short":"p.G118D","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"510/9093","CDS_position":"353/3207","Protein_position":"118/1068","Amino_acids":"G/D","Codons":"gGt/gAt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A2-A1FZ-01A-51D-A17G-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AN-A0FS-01A-11W-A050-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-LL-A5YN-01A-11D-A28B-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
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{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-BH-A0GY-01A-11W-A071-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
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{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218295,"End_Position":179218295,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-E2-A159-01A-11D-A10Y-09","HGVSc":"c.1625A>G","HGVSp":"p.Glu542Gly","HGVSp_Short":"p.E542G","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1782/9093","CDS_position":"1625/3207","Protein_position":"542/1068","Amino_acids":"E/G","Codons":"gAa/gGa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179203760,"End_Position":179203760,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-D8-A1JS-01A-11D-A13L-09","HGVSc":"c.1030G>A","HGVSp":"p.Val344Met","HGVSp_Short":"p.V344M","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1187/9093","CDS_position":"1030/3207","Protein_position":"344/1068","Amino_acids":"V/M","Codons":"Gtg/Atg"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-D8-A1JS-01A-11D-A13L-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A8-A07Z-01A-11W-A019-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218307,"End_Position":179218307,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AC-A23C-01A-12D-A167-09","HGVSc":"c.1637A>G","HGVSp":"p.Gln546Arg","HGVSp_Short":"p.Q546R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1794/9093","CDS_position":"1637/3207","Protein_position":"546/1068","Amino_acids":"Q/R","Codons":"cAg/cGg"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A7-A0CG-01A-11W-A019-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A8-A09C-01A-11W-A019-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179203765,"End_Position":179203765,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AR-A0TR-01A-11D-A099-09","HGVSc":"c.1035T>A","HGVSp":"p.Asn345Lys","HGVSp_Short":"p.N345K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1192/9093","CDS_position":"1035/3207","Protein_position":"345/1068","Amino_acids":"N/K","Codons":"aaT/aaA"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-BH-A1F8-01A-11D-A13L-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179203765,"End_Position":179203765,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A0HN-01A-11D-A099-09","HGVSc":"c.1035T>A","HGVSp":"p.Asn345Lys","HGVSp_Short":"p.N345K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1192/9093","CDS_position":"1035/3207","Protein_position":"345/1068","Amino_acids":"N/K","Codons":"aaT/aaA"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234287,"End_Position":179234287,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-E2-A14V-01A-11D-A12B-09","HGVSc":"c.3130A>T","HGVSp":"p.Asn1044Tyr","HGVSp_Short":"p.N1044Y","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3287/9093","CDS_position":"3130/3207","Protein_position":"1044/1068","Amino_acids":"N/Y","Codons":"Aat/Tat"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179210192,"End_Position":179210192,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"C","Tumor_Sample_Barcode":"TCGA-BH-A0DK-01A-21W-A071-09","HGVSc":"c.1258T>C","HGVSp":"p.Cys420Arg","HGVSp_Short":"p.C420R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1415/9093","CDS_position":"1258/3207","Protein_position":"420/1068","Amino_acids":"C/R","Codons":"Tgt/Cgt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-E2-A1L6-01A-11D-A13L-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A2-A0YC-01A-11D-A117-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A0DP-01A-21W-A071-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179203764,"End_Position":179203764,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"C","Tumor_Sample_Barcode":"TCGA-A7-A0D9-01A-31W-A071-09","HGVSc":"c.1034A>C","HGVSp":"p.Asn345Thr","HGVSp_Short":"p.N345T","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1191/9093","CDS_position":"1034/3207","Protein_position":"345/1068","Amino_acids":"N/T","Codons":"aAt/aCt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AQ-A54O-01A-11D-A25Q-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-XX-A89A-01A-11D-A36J-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179203765,"End_Position":179203765,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-E9-A226-01A-21D-A159-09","HGVSc":"c.1035T>A","HGVSp":"p.Asn345Lys","HGVSp_Short":"p.N345K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1192/9093","CDS_position":"1035/3207","Protein_position":"345/1068","Amino_acids":"N/K","Codons":"aaT/aaA"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179210192,"End_Position":179210192,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"C","Tumor_Sample_Barcode":"TCGA-D8-A1XL-01A-11D-A14K-09","HGVSc":"c.1258T>C","HGVSp":"p.Cys420Arg","HGVSp_Short":"p.C420R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1415/9093","CDS_position":"1258/3207","Protein_position":"420/1068","Amino_acids":"C/R","Codons":"Tgt/Cgt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A8-A08B-01A-11W-A019-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199035,"End_Position":179199035,"Variant_Classification":"Silent","Reference_Allele":"C","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-D8-A1Y1-01A-21D-A14K-09","HGVSc":"c.210C>T","HGVSp":"p.=","HGVSp_Short":"p.F70F","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"synonymous_variant","cDNA_position":"367/9093","CDS_position":"210/3207","Protein_position":"70/1068","Amino_acids":"F","Codons":"ttC/ttT"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-D8-A1Y1-01A-21D-A14K-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A7-A6VX-01A-12D-A33E-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AN-A049-01A-21W-A019-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234296,"End_Position":179234296,"Variant_Classification":"Missense_Mutation","Reference_Allele":"C","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-E2-A576-01A-11D-A31U-09","HGVSc":"c.3139C>T","HGVSp":"p.His1047Tyr","HGVSp_Short":"p.H1047Y","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3296/9093","CDS_position":"3139/3207","Protein_position":"1047/1068","Amino_acids":"H/Y","Codons":"Cat/Tat"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218306,"End_Position":179218306,"Variant_Classification":"Missense_Mutation","Reference_Allele":"C","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A8-A093-01A-11W-A019-09","HGVSc":"c.1636C>A","HGVSp":"p.Gln546Lys","HGVSp_Short":"p.Q546K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1793/9093","CDS_position":"1636/3207","Protein_position":"546/1068","Amino_acids":"Q/K","Codons":"Cag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199134,"End_Position":179199142,"Variant_Classification":"In_Frame_Del","Reference_Allele":"ACCAGTAGG","Tumor_Seq_Allele2":"-","Tumor_Sample_Barcode":"TCGA-C8-A26X-01A-31D-A16D-09","HGVSc":"c.309_317delACCAGTAGG","HGVSp":"p.Glu103_Gly106delinsAsp","HGVSp_Short":"p.E103_G106delinsD","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"inframe_deletion","cDNA_position":"466-474/9093","CDS_position":"309-317/3207","Protein_position":"103-106/1068","Amino_acids":"EPVG/D","Codons":"gaACCAGTAGGc/gac"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-OL-A66L-01A-12D-A31U-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A2-A0CR-01A-11D-A228-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-B6-A0RH-01A-21D-A10Y-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199066,"End_Position":179199066,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A0B6-01A-11D-A19Y-09","HGVSc":"c.241G>A","HGVSp":"p.Glu81Lys","HGVSp_Short":"p.E81K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"398/9093","CDS_position":"241/3207","Protein_position":"81/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179210291,"End_Position":179210291,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A0B6-01A-11D-A19Y-09","HGVSc":"c.1357G>A","HGVSp":"p.Glu453Lys","HGVSp_Short":"p.E453K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1514/9093","CDS_position":"1357/3207","Protein_position":"453/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-EW-A1J2-01A-21D-A13L-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-BH-A0EB-01A-11W-A050-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179203763,"End_Position":179203763,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"C","Tumor_Sample_Barcode":"TCGA-GM-A3NW-01A-21D-A228-09","HGVSc":"c.1033A>C","HGVSp":"p.Asn345His","HGVSp_Short":"p.N345H","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1190/9093","CDS_position":"1033/3207","Protein_position":"345/1068","Amino_acids":"N/H","Codons":"Aat/Cat"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A8-A07B-01A-11W-A019-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A2-A0EO-01A-11W-A050-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A8-A08Z-01A-21W-A019-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-C8-A130-01A-31D-A10Y-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199141,"End_Position":179199149,"Variant_Classification":"In_Frame_Del","Reference_Allele":"GGCAACCGT","Tumor_Seq_Allele2":"-","Tumor_Sample_Barcode":"TCGA-BH-A0HU-01A-11W-A050-09","HGVSc":"c.317_325delGCAACCGTG","HGVSp":"p.Gly106_Arg108del","HGVSp_Short":"p.G106_R108del","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"inframe_deletion","cDNA_position":"473-481/9093","CDS_position":"316-324/3207","Protein_position":"106-108/1068","Amino_acids":"GNR/-","Codons":"GGCAACCGT/-"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218307,"End_Position":179218307,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-EW-A1IW-01A-11D-A13L-09","HGVSc":"c.1637A>G","HGVSp":"p.Gln546Arg","HGVSp_Short":"p.Q546R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1794/9093","CDS_position":"1637/3207","Protein_position":"546/1068","Amino_acids":"Q/R","Codons":"cAg/cGg"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-C8-A1HE-01A-11D-A188-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A8-A08O-01A-21W-A071-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199690,"End_Position":179199690,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-LL-A9Q3-01A-11D-A41F-09","HGVSc":"c.353G>A","HGVSp":"p.Gly118Asp","HGVSp_Short":"p.G118D","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"510/9093","CDS_position":"353/3207","Protein_position":"118/1068","Amino_acids":"G/D","Codons":"gGt/gAt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179224185,"End_Position":179224185,"Variant_Classification":"Splice_Region","Reference_Allele":"C","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-E2-A152-01A-11D-A12B-09","HGVSc":"c.2292C>T","HGVSp":"p.=","HGVSp_Short":"p.L764L","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"splice_region_variant","cDNA_position":"2449/9093","CDS_position":"2292/3207","Protein_position":"764/1068","Amino_acids":"L","Codons":"ctC/ctT"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A5J0-01A-11D-A27P-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218304,"End_Position":179218304,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"C","Tumor_Sample_Barcode":"TCGA-BH-A8FY-01A-11D-A36J-09","HGVSc":"c.1634A>C","HGVSp":"p.Glu545Ala","HGVSp_Short":"p.E545A","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1791/9093","CDS_position":"1634/3207","Protein_position":"545/1068","Amino_acids":"E/A","Codons":"gAg/gCg"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179219657,"End_Position":179219657,"Variant_Classification":"Silent","Reference_Allele":"T","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-C8-A1HF-01A-11D-A135-09","HGVSc":"c.1833T>G","HGVSp":"p.=","HGVSp_Short":"p.V611V","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"synonymous_variant","cDNA_position":"1990/9093","CDS_position":"1833/3207","Protein_position":"611/1068","Amino_acids":"V","Codons":"gtT/gtG"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-C8-A1HF-01A-11D-A135-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AC-A23E-01A-11D-A159-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179219710,"End_Position":179219710,"Variant_Classification":"Missense_Mutation","Reference_Allele":"C","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AN-A04C-01A-21W-A050-09","HGVSc":"c.1886C>G","HGVSp":"p.Ser629Cys","HGVSp_Short":"p.S629C","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"2043/9093","CDS_position":"1886/3207","Protein_position":"629/1068","Amino_acids":"S/C","Codons":"tCt/tGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179203765,"End_Position":179203765,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-B6-A0RP-01A-21D-A099-09","HGVSc":"c.1035T>A","HGVSp":"p.Asn345Lys","HGVSp_Short":"p.N345K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1192/9093","CDS_position":"1035/3207","Protein_position":"345/1068","Amino_acids":"N/K","Codons":"aaT/aaA"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-E9-A1R4-01A-21D-A14G-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A2-A1G0-01A-11D-A13L-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-D8-A1JU-01A-11D-A13L-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199156,"End_Position":179199158,"Variant_Classification":"In_Frame_Del","Reference_Allele":"AAG","Tumor_Seq_Allele2":"-","Tumor_Sample_Barcode":"TCGA-BH-A0B5-01A-11D-A12Q-09","HGVSc":"c.332_334delAGA","HGVSp":"p.Lys111del","HGVSp_Short":"p.K111del","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"inframe_deletion","cDNA_position":"488-490/9093","CDS_position":"331-333/3207","Protein_position":"111/1068","Amino_acids":"K/-","Codons":"AAG/-"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179203765,"End_Position":179203765,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A0BF-01A-21D-A12Q-09","HGVSc":"c.1035T>A","HGVSp":"p.Asn345Lys","HGVSp_Short":"p.N345K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1192/9093","CDS_position":"1035/3207","Protein_position":"345/1068","Amino_acids":"N/K","Codons":"aaT/aaA"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A2-A0EN-01A-13D-A099-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-C8-A12L-01A-11D-A10Y-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-D8-A1XS-01A-11D-A14K-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-C8-A12U-01A-11D-A10Y-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179210291,"End_Position":179210291,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AO-A0JF-01A-11W-A071-09","HGVSc":"c.1357G>A","HGVSp":"p.Glu453Lys","HGVSp_Short":"p.E453K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1514/9093","CDS_position":"1357/3207","Protein_position":"453/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AO-A0JF-01A-11W-A071-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-B6-A0RG-01A-11W-A071-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-E2-A153-01A-12D-A12B-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-C8-A26W-01A-11D-A16D-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218304,"End_Position":179218304,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"C","Tumor_Sample_Barcode":"TCGA-BH-A0DE-01A-11D-A10Y-09","HGVSc":"c.1634A>C","HGVSp":"p.Glu545Ala","HGVSp_Short":"p.E545A","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1791/9093","CDS_position":"1634/3207","Protein_position":"545/1068","Amino_acids":"E/A","Codons":"gAg/gCg"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-EW-A423-01A-11D-A243-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AR-A1AV-01A-21D-A12Q-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199073,"End_Position":179199073,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"C","Tumor_Sample_Barcode":"TCGA-XX-A899-01A-11D-A36J-09","HGVSc":"c.248T>C","HGVSp":"p.Phe83Ser","HGVSp_Short":"p.F83S","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"405/9093","CDS_position":"248/3207","Protein_position":"83/1068","Amino_acids":"F/S","Codons":"tTt/tCt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179210272,"End_Position":179210298,"Variant_Classification":"In_Frame_Del","Reference_Allele":"GCCAGTACCTCATGGATTAGAAGATTT","Tumor_Seq_Allele2":"-","Tumor_Sample_Barcode":"TCGA-D8-A1JG-01B-11D-A13L-09","HGVSc":"c.1340_1366delCAGTACCTCATGGATTAGAAGATTTGC","HGVSp":"p.Pro447_Leu455del","HGVSp_Short":"p.P447_L455del","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"inframe_deletion","cDNA_position":"1495-1521/9093","CDS_position":"1338-1364/3207","Protein_position":"446-455/1068","Amino_acids":"WPVPHGLEDL/W","Codons":"tgGCCAGTACCTCATGGATTAGAAGATTTg/tgg"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-E2-A15E-01A-11D-A12B-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-A2-A0EM-01A-11W-A050-09","HGVSc":"c.3140A>T","HGVSp":"p.His1047Leu","HGVSp_Short":"p.H1047L","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/L","Codons":"cAt/cTt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-BH-A1EY-01A-11D-A13L-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AC-A5XS-01A-11D-A29N-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218304,"End_Position":179218304,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AC-A5XS-01A-11D-A29N-09","HGVSc":"c.1634A>G","HGVSp":"p.Glu545Gly","HGVSp_Short":"p.E545G","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1791/9093","CDS_position":"1634/3207","Protein_position":"545/1068","Amino_acids":"E/G","Codons":"gAg/gGg"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-JL-A3YX-01A-11D-A22X-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179221146,"End_Position":179221146,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-JL-A3YX-01A-11D-A22X-09","HGVSc":"c.2176G>A","HGVSp":"p.Glu726Lys","HGVSp_Short":"p.E726K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"2333/9093","CDS_position":"2176/3207","Protein_position":"726/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-C8-A274-01A-11D-A16D-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AR-A24T-01A-11D-A167-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A8-A08T-01A-21W-A019-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199156,"End_Position":179199164,"Variant_Classification":"In_Frame_Del","Reference_Allele":"AAGATCCTC","Tumor_Seq_Allele2":"-","Tumor_Sample_Barcode":"TCGA-AO-A03O-01A-11W-A019-09","HGVSc":"c.333_341delGATCCTCAA","HGVSp":"p.Lys111_Leu113del","HGVSp_Short":"p.K111_L113del","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"inframe_deletion","cDNA_position":"488-496/9093","CDS_position":"331-339/3207","Protein_position":"111-113/1068","Amino_acids":"KIL/-","Codons":"AAGATCCTC/-"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234287,"End_Position":179234287,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-EW-A1J1-01A-11D-A188-09","HGVSc":"c.3130A>T","HGVSp":"p.Asn1044Tyr","HGVSp_Short":"p.N1044Y","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3287/9093","CDS_position":"3130/3207","Protein_position":"1044/1068","Amino_acids":"N/Y","Codons":"Aat/Tat"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179221146,"End_Position":179221146,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A0W7-01A-11D-A10Y-09","HGVSc":"c.2176G>A","HGVSp":"p.Glu726Lys","HGVSp_Short":"p.E726K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"2333/9093","CDS_position":"2176/3207","Protein_position":"726/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-BH-A0W7-01A-11D-A10Y-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199156,"End_Position":179199156,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-BH-A1FE-01A-11D-A13L-09","HGVSc":"c.331A>G","HGVSp":"p.Lys111Glu","HGVSp_Short":"p.K111E","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"488/9093","CDS_position":"331/3207","Protein_position":"111/1068","Amino_acids":"K/E","Codons":"Aag/Gag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A2-A25A-01A-12D-A16D-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AC-A3OD-01A-11D-A21Q-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-BH-A0W5-01A-11D-A10G-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-E2-A1B4-01A-11D-A12Q-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-LL-A6FP-01A-11D-A31U-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A1ET-01A-11D-A135-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-E2-A15P-01A-11D-A10Y-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A8-A08L-01A-11W-A019-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199136,"End_Position":179199136,"Variant_Classification":"Missense_Mutation","Reference_Allele":"C","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-E9-A1RE-01A-11D-A159-09","HGVSc":"c.311C>T","HGVSp":"p.Pro104Leu","HGVSp_Short":"p.P104L","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"468/9093","CDS_position":"311/3207","Protein_position":"104/1068","Amino_acids":"P/L","Codons":"cCa/cTa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AR-A24M-01A-11D-A167-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A0B0-01A-21D-A10Y-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A0BV-01A-11W-A019-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199088,"End_Position":179199088,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-5L-AAT1-01A-12D-A41F-09","HGVSc":"c.263G>A","HGVSp":"p.Arg88Gln","HGVSp_Short":"p.R88Q","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"420/9093","CDS_position":"263/3207","Protein_position":"88/1068","Amino_acids":"R/Q","Codons":"cGa/cAa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-5L-AAT1-01A-12D-A41F-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-BH-A0BA-01A-11W-A071-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199150,"End_Position":179199152,"Variant_Classification":"In_Frame_Del","Reference_Allele":"GAA","Tumor_Seq_Allele2":"-","Tumor_Sample_Barcode":"TCGA-A2-A25D-01A-12D-A16D-09","HGVSc":"c.328_330delGAA","HGVSp":"p.Glu110del","HGVSp_Short":"p.E110del","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"inframe_deletion","cDNA_position":"482-484/9093","CDS_position":"325-327/3207","Protein_position":"109/1068","Amino_acids":"E/-","Codons":"GAA/-"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AR-A1AW-01A-21D-A12Q-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-BH-A203-01A-12D-A167-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179220987,"End_Position":179220987,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-EW-A1IZ-01A-11D-A188-09","HGVSc":"c.2017T>A","HGVSp":"p.Ser673Thr","HGVSp_Short":"p.S673T","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"2174/9093","CDS_position":"2017/3207","Protein_position":"673/1068","Amino_acids":"S/T","Codons":"Tct/Act"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-D8-A27L-01A-11D-A16D-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218286,"End_Position":179218286,"Variant_Classification":"Missense_Mutation","Reference_Allele":"C","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-B6-A0RO-01A-22D-A099-09","HGVSc":"c.1616C>G","HGVSp":"p.Pro539Arg","HGVSp_Short":"p.P539R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1773/9093","CDS_position":"1616/3207","Protein_position":"539/1068","Amino_acids":"P/R","Codons":"cCt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-B6-A0RO-01A-22D-A099-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-C8-A12Y-01A-11D-A12B-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-E9-A1R3-01A-31D-A14K-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-D8-A1JJ-01A-31D-A14K-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179210291,"End_Position":179210291,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-OL-A5DA-01A-11D-A27P-09","HGVSc":"c.1357G>A","HGVSp":"p.Glu453Lys","HGVSp_Short":"p.E453K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1514/9093","CDS_position":"1357/3207","Protein_position":"453/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179203765,"End_Position":179203765,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-OL-A5D6-01A-21D-A27P-09","HGVSc":"c.1035T>A","HGVSp":"p.Asn345Lys","HGVSp_Short":"p.N345K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1192/9093","CDS_position":"1035/3207","Protein_position":"345/1068","Amino_acids":"N/K","Codons":"aaT/aaA"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-E2-A15L-01A-11D-A12B-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179204540,"End_Position":179204540,"Variant_Classification":"Missense_Mutation","Reference_Allele":"C","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-OL-A5RX-01A-11D-A28B-09","HGVSc":"c.1097C>G","HGVSp":"p.Pro366Arg","HGVSp_Short":"p.P366R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1254/9093","CDS_position":"1097/3207","Protein_position":"366/1068","Amino_acids":"P/R","Codons":"cCc/cGc"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179230256,"End_Position":179230256,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-OL-A5RX-01A-11D-A28B-09","HGVSc":"c.2816A>G","HGVSp":"p.Asp939Gly","HGVSp_Short":"p.D939G","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"2973/9093","CDS_position":"2816/3207","Protein_position":"939/1068","Amino_acids":"D/G","Codons":"gAt/gGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A8-A06P-01A-11W-A019-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A2-A25C-01A-11D-A167-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-E9-A1R0-01A-22D-A16D-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AC-A5EH-01A-11D-A28B-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179209642,"End_Position":179209642,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-D8-A1JF-01A-11D-A13L-09","HGVSc":"c.1193G>A","HGVSp":"p.Arg398His","HGVSp_Short":"p.R398H","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1350/9093","CDS_position":"1193/3207","Protein_position":"398/1068","Amino_acids":"R/H","Codons":"cGt/cAt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-D8-A1JF-01A-11D-A13L-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-BH-A1EU-01A-11D-A135-09","HGVSc":"c.3140A>T","HGVSp":"p.His1047Leu","HGVSp_Short":"p.H1047L","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/L","Codons":"cAt/cTt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199150,"End_Position":179199152,"Variant_Classification":"In_Frame_Del","Reference_Allele":"GAA","Tumor_Seq_Allele2":"-","Tumor_Sample_Barcode":"TCGA-BH-A0HA-01A-11D-A12Q-09","HGVSc":"c.328_330delGAA","HGVSp":"p.Glu110del","HGVSp_Short":"p.E110del","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"inframe_deletion","cDNA_position":"482-484/9093","CDS_position":"325-327/3207","Protein_position":"109/1068","Amino_acids":"E/-","Codons":"GAA/-"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-BH-A0BD-01A-11W-A050-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A0DV-01A-21D-A12Q-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179221146,"End_Position":179221146,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A0DV-01A-21D-A12Q-09","HGVSc":"c.2176G>A","HGVSp":"p.Glu726Lys","HGVSp_Short":"p.E726K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"2333/9093","CDS_position":"2176/3207","Protein_position":"726/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179221147,"End_Position":179221147,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-BH-A0DV-01A-21D-A12Q-09","HGVSc":"c.2177A>G","HGVSp":"p.Glu726Gly","HGVSp_Short":"p.E726G","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"2334/9093","CDS_position":"2177/3207","Protein_position":"726/1068","Amino_acids":"E/G","Codons":"gAa/gGa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179203765,"End_Position":179203765,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A0BM-01A-11W-A071-09","HGVSc":"c.1035T>A","HGVSp":"p.Asn345Lys","HGVSp_Short":"p.N345K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1192/9093","CDS_position":"1035/3207","Protein_position":"345/1068","Amino_acids":"N/K","Codons":"aaT/aaA"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-D8-A1J8-01A-11D-A13L-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AR-A2LK-01A-11D-A17W-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179221146,"End_Position":179221146,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A2-A0CP-01A-11W-A050-09","HGVSc":"c.2176G>A","HGVSp":"p.Glu726Lys","HGVSp_Short":"p.E726K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"2333/9093","CDS_position":"2176/3207","Protein_position":"726/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A2-A0CP-01A-11W-A050-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179210291,"End_Position":179210291,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A8-A075-01A-11D-A099-09","HGVSc":"c.1357G>A","HGVSp":"p.Glu453Lys","HGVSp_Short":"p.E453K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1514/9093","CDS_position":"1357/3207","Protein_position":"453/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A8-A075-01A-11D-A099-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AO-A0JE-01A-11W-A071-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-E2-A15G-01A-11D-A12B-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A8-A092-01A-11W-A019-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179210272,"End_Position":179210298,"Variant_Classification":"In_Frame_Del","Reference_Allele":"GCCAGTACCTCATGGATTAGAAGATTT","Tumor_Seq_Allele2":"-","Tumor_Sample_Barcode":"TCGA-A8-A09B-01A-11W-A019-09","HGVSc":"c.1340_1366delCAGTACCTCATGGATTAGAAGATTTGC","HGVSp":"p.Pro447_Leu455del","HGVSp_Short":"p.P447_L455del","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"inframe_deletion","cDNA_position":"1495-1521/9093","CDS_position":"1338-1364/3207","Protein_position":"446-455/1068","Amino_acids":"WPVPHGLEDL/W","Codons":"tgGCCAGTACCTCATGGATTAGAAGATTTg/tgg"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179210291,"End_Position":179210291,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AN-A0XO-01A-11D-A10G-09","HGVSc":"c.1357G>A","HGVSp":"p.Glu453Lys","HGVSp_Short":"p.E453K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1514/9093","CDS_position":"1357/3207","Protein_position":"453/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-D8-A143-01A-11D-A10Y-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-HN-A2OB-01A-21D-A27P-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-BH-A0BO-01A-23D-A12B-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218307,"End_Position":179218307,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A7-A0CJ-01A-21W-A019-09","HGVSc":"c.1637A>G","HGVSp":"p.Gln546Arg","HGVSp_Short":"p.Q546R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1794/9093","CDS_position":"1637/3207","Protein_position":"546/1068","Amino_acids":"Q/R","Codons":"cAg/cGg"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-D8-A27P-01A-11D-A16D-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A8-A09D-01A-11W-A019-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A8-A0A1-01A-11W-A019-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234176,"End_Position":179234176,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"C","Tumor_Sample_Barcode":"TCGA-BH-A0H9-01A-11W-A071-09","HGVSc":"c.3019G>C","HGVSp":"p.Gly1007Arg","HGVSp_Short":"p.G1007R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3176/9093","CDS_position":"3019/3207","Protein_position":"1007/1068","Amino_acids":"G/R","Codons":"Ggc/Cgc"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A2-A0EX-01A-21W-A050-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AC-A2B8-01A-11D-A17D-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AO-A0JA-01A-11W-A071-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234266,"End_Position":179234266,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A18H-01A-11D-A12B-09","HGVSc":"c.3109G>A","HGVSp":"p.Glu1037Lys","HGVSp_Short":"p.E1037K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3266/9093","CDS_position":"3109/3207","Protein_position":"1037/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-D8-A1JE-01A-11D-A13L-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199156,"End_Position":179199158,"Variant_Classification":"In_Frame_Del","Reference_Allele":"AAG","Tumor_Seq_Allele2":"-","Tumor_Sample_Barcode":"TCGA-D8-A27K-01A-11D-A16D-09","HGVSc":"c.332_334delAGA","HGVSp":"p.Lys111del","HGVSp_Short":"p.K111del","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"inframe_deletion","cDNA_position":"488-490/9093","CDS_position":"331-333/3207","Protein_position":"111/1068","Amino_acids":"K/-","Codons":"AAG/-"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A2-A0YL-01A-21D-A10G-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-B6-A0X5-01A-21D-A10G-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A2-A0T4-01A-31D-A099-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A8-A096-01A-11W-A019-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AC-A3YJ-01A-11D-A22X-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-E2-A14Y-01A-21D-A12B-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234286,"End_Position":179234286,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A0DO-01B-11D-A12B-09","HGVSc":"c.3129G>A","HGVSp":"p.Met1043Ile","HGVSp_Short":"p.M1043I","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3286/9093","CDS_position":"3129/3207","Protein_position":"1043/1068","Amino_acids":"M/I","Codons":"atG/atA"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234302,"End_Position":179234302,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"C","Tumor_Sample_Barcode":"TCGA-BH-A2L8-01A-11D-A18P-09","HGVSc":"c.3145G>C","HGVSp":"p.Gly1049Arg","HGVSp_Short":"p.G1049R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3302/9093","CDS_position":"3145/3207","Protein_position":"1049/1068","Amino_acids":"G/R","Codons":"Ggt/Cgt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A8-A08P-01A-11W-A019-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234302,"End_Position":179234302,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"C","Tumor_Sample_Barcode":"TCGA-A2-A0CW-01A-21D-A10Y-09","HGVSc":"c.3145G>C","HGVSp":"p.Gly1049Arg","HGVSp_Short":"p.G1049R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3302/9093","CDS_position":"3145/3207","Protein_position":"1049/1068","Amino_acids":"G/R","Codons":"Ggt/Cgt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199148,"End_Position":179199148,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-C8-A131-01A-11D-A10Y-09","HGVSc":"c.323G>A","HGVSp":"p.Arg108His","HGVSp_Short":"p.R108H","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"480/9093","CDS_position":"323/3207","Protein_position":"108/1068","Amino_acids":"R/H","Codons":"cGt/cAt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-C8-A131-01A-11D-A10Y-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AN-A0XS-01A-22D-A10G-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-B6-A0IK-01A-12W-A071-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A8-A07G-01A-11W-A050-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-E2-A156-01A-11D-A12B-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179221146,"End_Position":179221146,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A8-A0A7-01A-11W-A019-09","HGVSc":"c.2176G>A","HGVSp":"p.Glu726Lys","HGVSp_Short":"p.E726K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"2333/9093","CDS_position":"2176/3207","Protein_position":"726/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
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{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179203765,"End_Position":179203765,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-E9-A3X8-01A-31D-A22X-09","HGVSc":"c.1035T>A","HGVSp":"p.Asn345Lys","HGVSp_Short":"p.N345K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1192/9093","CDS_position":"1035/3207","Protein_position":"345/1068","Amino_acids":"N/K","Codons":"aaT/aaA"}
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{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-D8-A146-01A-31D-A10Y-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-EW-A6SC-01A-12D-A32I-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-D8-A3Z6-01A-11D-A23C-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AR-A5QP-01A-11D-A28B-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-B6-A0IE-01A-11W-A050-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-GM-A2DD-01A-11D-A17W-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218306,"End_Position":179218306,"Variant_Classification":"Missense_Mutation","Reference_Allele":"C","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A18F-01A-11D-A12B-09","HGVSc":"c.1636C>A","HGVSp":"p.Gln546Lys","HGVSp_Short":"p.Q546K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1793/9093","CDS_position":"1636/3207","Protein_position":"546/1068","Amino_acids":"Q/K","Codons":"Cag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-BH-A18F-01A-11D-A12B-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AR-A24S-01A-11D-A167-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A2-A0D1-01A-11W-A050-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218307,"End_Position":179218307,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-GM-A2DH-01A-11D-A17W-09","HGVSc":"c.1637A>G","HGVSp":"p.Gln546Arg","HGVSp_Short":"p.Q546R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1794/9093","CDS_position":"1637/3207","Protein_position":"546/1068","Amino_acids":"Q/R","Codons":"cAg/cGg"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234176,"End_Position":179234176,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"C","Tumor_Sample_Barcode":"TCGA-GM-A2DH-01A-11D-A17W-09","HGVSc":"c.3019G>C","HGVSp":"p.Gly1007Arg","HGVSp_Short":"p.G1007R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3176/9093","CDS_position":"3019/3207","Protein_position":"1007/1068","Amino_acids":"G/R","Codons":"Ggc/Cgc"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-B6-A40B-01A-11D-A23C-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-D8-A1Y2-01A-11D-A159-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-S3-AA14-01A-11D-A41F-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199066,"End_Position":179199066,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-EW-A1OV-01A-11D-A142-09","HGVSc":"c.241G>A","HGVSp":"p.Glu81Lys","HGVSp_Short":"p.E81K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"398/9093","CDS_position":"241/3207","Protein_position":"81/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-D8-A73U-01A-11D-A33E-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179210302,"End_Position":179210302,"Variant_Classification":"Silent","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AC-A23H-01A-11D-A159-09","HGVSc":"c.1368G>A","HGVSp":"p.=","HGVSp_Short":"p.L456L","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"synonymous_variant","cDNA_position":"1525/9093","CDS_position":"1368/3207","Protein_position":"456/1068","Amino_acids":"L","Codons":"ctG/ctA"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179219631,"End_Position":179219631,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"C","Tumor_Sample_Barcode":"TCGA-AC-A23H-01A-11D-A159-09","HGVSc":"c.1807G>C","HGVSp":"p.Asp603His","HGVSp_Short":"p.D603H","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1964/9093","CDS_position":"1807/3207","Protein_position":"603/1068","Amino_acids":"D/H","Codons":"Gac/Cac"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234122,"End_Position":179234122,"Variant_Classification":"Missense_Mutation","Reference_Allele":"C","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AC-A23H-01A-11D-A159-09","HGVSc":"c.2965C>G","HGVSp":"p.Leu989Val","HGVSp_Short":"p.L989V","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3122/9093","CDS_position":"2965/3207","Protein_position":"989/1068","Amino_acids":"L/V","Codons":"Cta/Gta"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218307,"End_Position":179218307,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"C","Tumor_Sample_Barcode":"TCGA-B6-A1KI-01A-11D-A14K-09","HGVSc":"c.1637A>C","HGVSp":"p.Gln546Pro","HGVSp_Short":"p.Q546P","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1794/9093","CDS_position":"1637/3207","Protein_position":"546/1068","Amino_acids":"Q/P","Codons":"cAg/cCg"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218295,"End_Position":179218295,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-B6-A0RQ-01A-11D-A10Y-09","HGVSc":"c.1625A>G","HGVSp":"p.Glu542Gly","HGVSp_Short":"p.E542G","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1782/9093","CDS_position":"1625/3207","Protein_position":"542/1068","Amino_acids":"E/G","Codons":"gAa/gGa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A8-A0A9-01A-11W-A019-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-E2-A1IN-01A-11D-A13L-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A0BQ-01A-21D-A10Y-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179210291,"End_Position":179210291,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-GM-A2D9-01A-11D-A18P-09","HGVSc":"c.1357G>A","HGVSp":"p.Glu453Lys","HGVSp_Short":"p.E453K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1514/9093","CDS_position":"1357/3207","Protein_position":"453/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-GM-A2D9-01A-11D-A18P-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A0W3-01A-11D-A10G-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179224158,"End_Position":179224158,"Variant_Classification":"Silent","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A8-A09Q-01A-11W-A019-09","HGVSc":"c.2265A>G","HGVSp":"p.=","HGVSp_Short":"p.L755L","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"synonymous_variant","cDNA_position":"2422/9093","CDS_position":"2265/3207","Protein_position":"755/1068","Amino_acids":"L","Codons":"ctA/ctG"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179203765,"End_Position":179203765,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A2-A0YH-01A-11D-A10G-09","HGVSc":"c.1035T>A","HGVSp":"p.Asn345Lys","HGVSp_Short":"p.N345K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1192/9093","CDS_position":"1035/3207","Protein_position":"345/1068","Amino_acids":"N/K","Codons":"aaT/aaA"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234286,"End_Position":179234286,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"C","Tumor_Sample_Barcode":"TCGA-C8-A3M8-01A-11D-A20S-09","HGVSc":"c.3129G>C","HGVSp":"p.Met1043Ile","HGVSp_Short":"p.M1043I","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3286/9093","CDS_position":"3129/3207","Protein_position":"1043/1068","Amino_acids":"M/I","Codons":"atG/atC"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218304,"End_Position":179218304,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"C","Tumor_Sample_Barcode":"TCGA-AC-A6NO-01A-12D-A33E-09","HGVSc":"c.1634A>C","HGVSp":"p.Glu545Ala","HGVSp_Short":"p.E545A","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1791/9093","CDS_position":"1634/3207","Protein_position":"545/1068","Amino_acids":"E/A","Codons":"gAg/gCg"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199690,"End_Position":179199690,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A2-A0EY-01A-11W-A050-09","HGVSc":"c.353G>A","HGVSp":"p.Gly118Asp","HGVSp_Short":"p.G118D","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"510/9093","CDS_position":"353/3207","Protein_position":"118/1068","Amino_acids":"G/D","Codons":"gGt/gAt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-B6-A0IC-01A-11W-A050-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-C8-A3M7-01A-12D-A21Q-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179224701,"End_Position":179224701,"Variant_Classification":"Missense_Mutation","Reference_Allele":"C","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-BH-A0EE-01A-11W-A050-09","HGVSc":"c.2296C>T","HGVSp":"p.Leu766Phe","HGVSp_Short":"p.L766F","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"2453/9093","CDS_position":"2296/3207","Protein_position":"766/1068","Amino_acids":"L/F","Codons":"Ctt/Ttt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-C8-A133-01A-32D-A12B-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-EW-A1J5-01A-11D-A13L-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179221146,"End_Position":179221146,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-EW-A1J5-01A-11D-A13L-09","HGVSc":"c.2176G>A","HGVSp":"p.Glu726Lys","HGVSp_Short":"p.E726K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"2333/9093","CDS_position":"2176/3207","Protein_position":"726/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A18I-01A-11D-A12B-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A0HI-01A-11D-A099-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-E9-A229-01A-31D-A17G-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-E9-A1NI-01A-11W-A16H-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-LL-A7T0-01A-31D-A351-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-D8-A73X-01A-11D-A32I-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-B6-A0RN-01A-12D-A099-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A8-A081-01A-11W-A019-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-C8-A12T-01A-11D-A10Y-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A0DT-01A-21D-A12B-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179210279,"End_Position":179210305,"Variant_Classification":"In_Frame_Del","Reference_Allele":"CCTCATGGATTAGAAGATTTGCTGAAC","Tumor_Seq_Allele2":"-","Tumor_Sample_Barcode":"TCGA-A8-A07J-01A-11W-A019-09","HGVSc":"c.1348_1374delCATGGATTAGAAGATTTGCTGAACCCT","HGVSp":"p.His450_Pro458del","HGVSp_Short":"p.H450_P458del","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"inframe_deletion","cDNA_position":"1502-1528/9093","CDS_position":"1345-1371/3207","Protein_position":"449-457/1068","Amino_acids":"PHGLEDLLN/-","Codons":"CCTCATGGATTAGAAGATTTGCTGAAC/-"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-E9-A1RI-01A-11D-A167-09","HGVSc":"c.3140A>T","HGVSp":"p.His1047Leu","HGVSp_Short":"p.H1047L","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/L","Codons":"cAt/cTt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-5L-AAT0-01A-12D-A41F-09","HGVSc":"c.3140A>T","HGVSp":"p.His1047Leu","HGVSp_Short":"p.H1047L","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/L","Codons":"cAt/cTt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-BH-A0BC-01A-22D-A099-09","HGVSc":"c.3140A>T","HGVSp":"p.His1047Leu","HGVSp_Short":"p.H1047L","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/L","Codons":"cAt/cTt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A2-A0SY-01A-31D-A099-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218307,"End_Position":179218307,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-B6-A0I5-01A-11W-A100-09","HGVSc":"c.1637A>G","HGVSp":"p.Gln546Arg","HGVSp_Short":"p.Q546R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1794/9093","CDS_position":"1637/3207","Protein_position":"546/1068","Amino_acids":"Q/R","Codons":"cAg/cGg"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179221146,"End_Position":179221146,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A1-A0SI-01A-11D-A142-09","HGVSc":"c.2176G>A","HGVSp":"p.Glu726Lys","HGVSp_Short":"p.E726K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"2333/9093","CDS_position":"2176/3207","Protein_position":"726/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A1-A0SI-01A-11D-A142-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-E9-A1NG-01A-21D-A14K-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199152,"End_Position":179199160,"Variant_Classification":"In_Frame_Del","Reference_Allele":"AGAAAAGAT","Tumor_Seq_Allele2":"-","Tumor_Sample_Barcode":"TCGA-B6-A0WY-01A-11D-A10G-09","HGVSc":"c.327_335delAGAAAAGAT","HGVSp":"p.Glu109_Ile112delinsAsp","HGVSp_Short":"p.E109_I112delinsD","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"inframe_deletion","cDNA_position":"484-492/9093","CDS_position":"327-335/3207","Protein_position":"109-112/1068","Amino_acids":"EEKI/D","Codons":"gaAGAAAAGATc/gac"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-D8-A1JD-01A-11D-A13L-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179221146,"End_Position":179221146,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-D8-A1JD-01A-11D-A13L-09","HGVSc":"c.2176G>A","HGVSp":"p.Glu726Lys","HGVSp_Short":"p.E726K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"2333/9093","CDS_position":"2176/3207","Protein_position":"726/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234169,"End_Position":179234169,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-D8-A1JD-01A-11D-A13L-09","HGVSc":"c.3012G>A","HGVSp":"p.Met1004Ile","HGVSp_Short":"p.M1004I","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3169/9093","CDS_position":"3012/3207","Protein_position":"1004/1068","Amino_acids":"M/I","Codons":"atG/atA"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AO-A0J5-01A-11W-A050-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A7-A26H-01A-11D-A167-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179210284,"End_Position":179210310,"Variant_Classification":"In_Frame_Del","Reference_Allele":"TGGATTAGAAGATTTGCTGAACCCTAT","Tumor_Seq_Allele2":"-","Tumor_Sample_Barcode":"TCGA-BH-A201-01A-11D-A14K-09","HGVSc":"c.1353_1379delATTAGAAGATTTGCTGAACCCTATTGG","HGVSp":"p.Leu452_Gly460del","HGVSp_Short":"p.L452_G460del","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"inframe_deletion","cDNA_position":"1507-1533/9093","CDS_position":"1350-1376/3207","Protein_position":"450-459/1068","Amino_acids":"HGLEDLLNPI/H","Codons":"caTGGATTAGAAGATTTGCTGAACCCTATt/cat"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A8-A06Q-01A-11W-A050-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179203765,"End_Position":179203765,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AR-A2LM-01A-11D-A17W-09","HGVSc":"c.1035T>A","HGVSp":"p.Asn345Lys","HGVSp_Short":"p.N345K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1192/9093","CDS_position":"1035/3207","Protein_position":"345/1068","Amino_acids":"N/K","Codons":"aaT/aaA"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AR-A0TZ-01A-12D-A099-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-BH-A0DL-01A-11D-A10Y-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179210272,"End_Position":179210298,"Variant_Classification":"In_Frame_Del","Reference_Allele":"GCCAGTACCTCATGGATTAGAAGATTT","Tumor_Seq_Allele2":"-","Tumor_Sample_Barcode":"TCGA-EW-A1P5-01A-11D-A142-09","HGVSc":"c.1340_1366delCAGTACCTCATGGATTAGAAGATTTGC","HGVSp":"p.Pro447_Leu455del","HGVSp_Short":"p.P447_L455del","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"inframe_deletion","cDNA_position":"1495-1521/9093","CDS_position":"1338-1364/3207","Protein_position":"446-455/1068","Amino_acids":"WPVPHGLEDL/W","Codons":"tgGCCAGTACCTCATGGATTAGAAGATTTg/tgg"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A8-A06R-01A-11D-A015-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-AN-A03X-01A-21W-A019-09","HGVSc":"c.3140A>T","HGVSp":"p.His1047Leu","HGVSp_Short":"p.H1047L","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/L","Codons":"cAt/cTt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A7-A5ZW-01A-12D-A29N-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179203765,"End_Position":179203765,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AR-A255-01A-11D-A167-09","HGVSc":"c.1035T>A","HGVSp":"p.Asn345Lys","HGVSp_Short":"p.N345K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1192/9093","CDS_position":"1035/3207","Protein_position":"345/1068","Amino_acids":"N/K","Codons":"aaT/aaA"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179219622,"End_Position":179219622,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AQ-A7U7-01A-22D-A351-09","HGVSc":"c.1798G>A","HGVSp":"p.Glu600Lys","HGVSp_Short":"p.E600K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1955/9093","CDS_position":"1798/3207","Protein_position":"600/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199088,"End_Position":179199088,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A2-A04P-01A-31D-A128-09","HGVSc":"c.263G>A","HGVSp":"p.Arg88Gln","HGVSp_Short":"p.R88Q","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"420/9093","CDS_position":"263/3207","Protein_position":"88/1068","Amino_acids":"R/Q","Codons":"cGa/cAa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-E2-A1BC-01A-11D-A14G-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AN-A03Y-01A-21W-A019-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AC-A2FO-01A-11D-A17W-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A2-A0YT-01A-11D-A10G-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179203765,"End_Position":179203765,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-B6-A401-01A-11D-A23C-09","HGVSc":"c.1035T>A","HGVSp":"p.Asn345Lys","HGVSp_Short":"p.N345K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1192/9093","CDS_position":"1035/3207","Protein_position":"345/1068","Amino_acids":"N/K","Codons":"aaT/aaA"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-E2-A1IF-01A-11D-A142-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-E9-A295-01A-11D-A16D-09","HGVSc":"c.3140A>T","HGVSp":"p.His1047Leu","HGVSp_Short":"p.H1047L","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/L","Codons":"cAt/cTt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199138,"End_Position":179199149,"Variant_Classification":"In_Frame_Del","Reference_Allele":"GTAGGCAACCGT","Tumor_Seq_Allele2":"-","Tumor_Sample_Barcode":"TCGA-D8-A1XB-01A-11D-A14G-09","HGVSc":"c.314_325delTAGGCAACCGTG","HGVSp":"p.Val105_Arg108del","HGVSp_Short":"p.V105_R108del","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"inframe_deletion","cDNA_position":"470-481/9093","CDS_position":"313-324/3207","Protein_position":"105-108/1068","Amino_acids":"VGNR/-","Codons":"GTAGGCAACCGT/-"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AN-A0FF-01A-11W-A050-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-E2-A10C-01A-21D-A10M-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-E9-A249-01A-11D-A167-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-Z7-A8R5-01A-42D-A41F-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179204537,"End_Position":179204537,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-BH-A202-01A-11D-A14K-09","HGVSc":"c.1094A>T","HGVSp":"p.Glu365Val","HGVSp_Short":"p.E365V","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1251/9093","CDS_position":"1094/3207","Protein_position":"365/1068","Amino_acids":"E/V","Codons":"gAa/gTa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-BH-A202-01A-11D-A14K-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A7-A26E-01A-11D-A272-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-D8-A1JN-01A-11D-A13L-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-E2-A1IO-01A-11D-A142-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-E9-A1RA-01A-11D-A14G-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-E2-A15K-01A-11D-A12Q-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-D8-A27T-01A-11D-A16D-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179219664,"End_Position":179219664,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A8-A08R-01A-11W-A050-09","HGVSc":"c.1840T>A","HGVSp":"p.Phe614Ile","HGVSp_Short":"p.F614I","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1997/9093","CDS_position":"1840/3207","Protein_position":"614/1068","Amino_acids":"F/I","Codons":"Ttt/Att"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179204540,"End_Position":179204540,"Variant_Classification":"Missense_Mutation","Reference_Allele":"C","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-BH-A0BT-01A-11D-A12Q-09","HGVSc":"c.1097C>G","HGVSp":"p.Pro366Arg","HGVSp_Short":"p.P366R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1254/9093","CDS_position":"1097/3207","Protein_position":"366/1068","Amino_acids":"P/R","Codons":"cCc/cGc"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-BH-A0BT-01A-11D-A12Q-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A2-A0D3-01A-11D-A10Y-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-E9-A1RD-01A-11D-A159-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-D8-A1JK-01A-11D-A13L-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179203765,"End_Position":179203765,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A2-A0YI-01A-31D-A10M-09","HGVSc":"c.1035T>A","HGVSp":"p.Asn345Lys","HGVSp_Short":"p.N345K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1192/9093","CDS_position":"1035/3207","Protein_position":"345/1068","Amino_acids":"N/K","Codons":"aaT/aaA"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A2-A0CS-01A-11D-A10Y-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A2-A0EQ-01A-11W-A050-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234296,"End_Position":179234296,"Variant_Classification":"Missense_Mutation","Reference_Allele":"C","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-A2-A04T-01A-21W-A050-09","HGVSc":"c.3139C>T","HGVSp":"p.His1047Tyr","HGVSp_Short":"p.H1047Y","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3296/9093","CDS_position":"3139/3207","Protein_position":"1047/1068","Amino_acids":"H/Y","Codons":"Cat/Tat"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179203765,"End_Position":179203765,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A0H3-01A-11D-A12Q-09","HGVSc":"c.1035T>A","HGVSp":"p.Asn345Lys","HGVSp_Short":"p.N345K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1192/9093","CDS_position":"1035/3207","Protein_position":"345/1068","Amino_acids":"N/K","Codons":"aaT/aaA"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-B6-A0WW-01A-11D-A10G-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A0DX-01A-11D-A10Y-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A7-A0DB-01A-11D-A272-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199132,"End_Position":179199137,"Variant_Classification":"In_Frame_Del","Reference_Allele":"GAACCA","Tumor_Seq_Allele2":"-","Tumor_Sample_Barcode":"TCGA-E9-A1RH-01A-21D-A167-09","HGVSc":"c.308_313delAACCAG","HGVSp":"p.Glu103_Pro104del","HGVSp_Short":"p.E103_P104del","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"inframe_deletion","cDNA_position":"464-469/9093","CDS_position":"307-312/3207","Protein_position":"103-104/1068","Amino_acids":"EP/-","Codons":"GAACCA/-"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179203765,"End_Position":179203765,"Variant_Classification":"Missense_Mutation","Reference_Allele":"T","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AO-A03L-01A-41W-A071-09","HGVSc":"c.1035T>A","HGVSp":"p.Asn345Lys","HGVSp_Short":"p.N345K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1192/9093","CDS_position":"1035/3207","Protein_position":"345/1068","Amino_acids":"N/K","Codons":"aaT/aaA"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AR-A5QM-01A-11D-A27P-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A0HF-01A-11W-A071-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-D8-A1XO-01A-11D-A14K-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-LD-A66U-01A-11D-A31U-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A8-A06U-01A-11W-A019-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199690,"End_Position":179199690,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-A8-A0A6-01A-12W-A071-09","HGVSc":"c.353G>A","HGVSp":"p.Gly118Asp","HGVSp_Short":"p.G118D","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"510/9093","CDS_position":"353/3207","Protein_position":"118/1068","Amino_acids":"G/D","Codons":"gGt/gAt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179230256,"End_Position":179230256,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-EW-A1P0-01A-11D-A142-09","HGVSc":"c.2816A>G","HGVSp":"p.Asp939Gly","HGVSp_Short":"p.D939G","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"2973/9093","CDS_position":"2816/3207","Protein_position":"939/1068","Amino_acids":"D/G","Codons":"gAt/gGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-LL-A50Y-01A-11D-A25Q-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234169,"End_Position":179234169,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AO-A1KR-01A-12D-A142-09","HGVSc":"c.3012G>A","HGVSp":"p.Met1004Ile","HGVSp_Short":"p.M1004I","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3169/9093","CDS_position":"3012/3207","Protein_position":"1004/1068","Amino_acids":"M/I","Codons":"atG/atA"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AO-A1KR-01A-12D-A142-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179210431,"End_Position":179210432,"Variant_Classification":"Splice_Region","Reference_Allele":"-","Tumor_Seq_Allele2":"ATA","Tumor_Sample_Barcode":"TCGA-A2-A0EV-01A-11W-A050-09","HGVSc":"c.1406_1407insTAA","HGVSp":"p.Glu469delinsAspLys","HGVSp_Short":"p.E469delinsDK","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"splice_region_variant","cDNA_position":"1562-1563/9093","CDS_position":"1405-1406/3207","Protein_position":"469/1068","Amino_acids":"E/DK","Codons":"gaa/gATAaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A2-A0EV-01A-11W-A050-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-D8-A1XY-01A-11D-A14K-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218304,"End_Position":179218304,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"C","Tumor_Sample_Barcode":"TCGA-S3-AA11-01A-31D-A41F-09","HGVSc":"c.1634A>C","HGVSp":"p.Glu545Ala","HGVSp_Short":"p.E545A","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1791/9093","CDS_position":"1634/3207","Protein_position":"545/1068","Amino_acids":"E/A","Codons":"gAg/gCg"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-EW-A1IX-01A-12D-A142-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-C8-A8HQ-01A-11D-A36J-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-AC-A8OS-01A-12D-A41F-09","HGVSc":"c.3140A>T","HGVSp":"p.His1047Leu","HGVSp_Short":"p.H1047L","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/L","Codons":"cAt/cTt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-C8-A12N-01A-11D-A10Y-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-EW-A2FV-01A-11D-A17D-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179203779,"End_Position":179203779,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AR-A24K-01A-11D-A167-09","HGVSc":"c.1049A>G","HGVSp":"p.Asp350Gly","HGVSp_Short":"p.D350G","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1206/9093","CDS_position":"1049/3207","Protein_position":"350/1068","Amino_acids":"D/G","Codons":"gAc/gGc"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-AQ-A1H2-01A-11D-A13L-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-PE-A5DE-01A-11D-A27P-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-GM-A2DI-01A-31D-A18P-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-BH-A0EA-01A-11D-A10Y-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
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{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-BH-A42V-01A-11D-A243-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-E2-A1L8-01A-11D-A13L-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-E2-A154-01A-11D-A10Y-09","HGVSc":"c.3140A>T","HGVSp":"p.His1047Leu","HGVSp_Short":"p.H1047L","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/L","Codons":"cAt/cTt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179199690,"End_Position":179199690,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-WT-AB41-01A-11D-A41F-09","HGVSc":"c.353G>A","HGVSp":"p.Gly118Asp","HGVSp_Short":"p.G118D","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"510/9093","CDS_position":"353/3207","Protein_position":"118/1068","Amino_acids":"G/D","Codons":"gGt/gAt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218306,"End_Position":179218306,"Variant_Classification":"Missense_Mutation","Reference_Allele":"C","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-EW-A1PE-01A-11D-A142-09","HGVSc":"c.1636C>A","HGVSp":"p.Gln546Lys","HGVSp_Short":"p.Q546K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1793/9093","CDS_position":"1636/3207","Protein_position":"546/1068","Amino_acids":"Q/K","Codons":"Cag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234230,"End_Position":179234230,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-EW-A1PE-01A-11D-A142-09","HGVSc":"c.3073A>G","HGVSp":"p.Thr1025Ala","HGVSp_Short":"p.T1025A","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3230/9093","CDS_position":"3073/3207","Protein_position":"1025/1068","Amino_acids":"T/A","Codons":"Acc/Gcc"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218303,"End_Position":179218303,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-AN-A0AK-01A-21W-A019-09","HGVSc":"c.1633G>A","HGVSp":"p.Glu545Lys","HGVSp_Short":"p.E545K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1790/9093","CDS_position":"1633/3207","Protein_position":"545/1068","Amino_acids":"E/K","Codons":"Gag/Aag"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-E9-A227-01A-11D-A159-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-D8-A1XM-01A-21D-A14K-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-D8-A1JH-01A-11D-A188-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218294,"End_Position":179218294,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"A","Tumor_Sample_Barcode":"TCGA-3C-AALK-01A-11D-A41F-09","HGVSc":"c.1624G>A","HGVSp":"p.Glu542Lys","HGVSp_Short":"p.E542K","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1781/9093","CDS_position":"1624/3207","Protein_position":"542/1068","Amino_acids":"E/K","Codons":"Gaa/Aaa"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234169,"End_Position":179234169,"Variant_Classification":"Missense_Mutation","Reference_Allele":"G","Tumor_Seq_Allele2":"T","Tumor_Sample_Barcode":"TCGA-3C-AALK-01A-11D-A41F-09","HGVSc":"c.3012G>T","HGVSp":"p.Met1004Ile","HGVSp_Short":"p.M1004I","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3169/9093","CDS_position":"3012/3207","Protein_position":"1004/1068","Amino_acids":"M/I","Codons":"atG/atT"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179218307,"End_Position":179218307,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-A2-A0EW-01A-21D-A10Y-09","HGVSc":"c.1637A>G","HGVSp":"p.Gln546Arg","HGVSp_Short":"p.Q546R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"1794/9093","CDS_position":"1637/3207","Protein_position":"546/1068","Amino_acids":"Q/R","Codons":"cAg/cGg"}
{"Hugo_Symbol":"PIK3CA","Chromosome":"chr3","Start_Position":179234297,"End_Position":179234297,"Variant_Classification":"Missense_Mutation","Reference_Allele":"A","Tumor_Seq_Allele2":"G","Tumor_Sample_Barcode":"TCGA-E2-A1IL-01A-11D-A14G-09","HGVSc":"c.3140A>G","HGVSp":"p.His1047Arg","HGVSp_Short":"p.H1047R","Transcript_ID":"ENST00000263967","Gene":"ENSG00000121879","One_Consequence":"missense_variant","cDNA_position":"3297/9093","CDS_position":"3140/3207","Protein_position":"1047/1068","Amino_acids":"H/R","Codons":"cAt/cGt"}