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{"Hugo_Symbol":"ABHD12","Entrez_Gene_Id":26090,"Center":"hgsc.bcm.edu","NCBI_Build":36,"Chromosome":20,"Start_position":25248888,"End_position":25248888,"Strand":"+","Variant_Classification":"Silent","Variant_Type":"SNP","Reference_Allele":"G","Tumor_Seq_Allele1":"G","Tumor_Seq_Allele2":"T","dbSNP_RS":"novel","dbSNP_Val_Status":"unknown","Tumor_Sample_Barcode":"TCGA-A6-2676-01A-01W-0833-10","Matched_Norm_Sample_Barcode":"TCGA-A6-2676-10A-01W-0833-10","Match_Norm_Seq_Allele1":"G","Match_Norm_Seq_Allele2":"G","Tumor_Validation_Allele1":"G","Tumor_Validation_Allele2":"T","Match_Norm_Validation_Allele1":"G","Match_Norm_Validation_Allele2":"G","Verification_Status":"Unknown","Validation_Status":"Valid","Mutation_Status":"Somatic","Sequencing_Phase":"Phase_I","Sequence_Source":"Capture","Validation_Method":"Illumina","Sequencer":"SOLID","TranscriptID":"NM_001042472","Exon":"exon4","ChromChange":"c.C489A","AAChange":"p.A163A","COSMIC_Codon":".","COSMIC_Gene":".","Drug_Target":".","MA.link.var":"http://getma.org/v1/?cm=var&var=hg18","MA":20,"MA.variant":"25248888","MA.protein.change":"G","MA.Gene":"T&fts=all","MA.link.MSA":1,"MA.link.PDB":"hg18","MA.FImpact":"20","MA.FI.score":"25248888","MA.Cytoband":"G","MA.Uniprot":"T","MA.Refseq":"A163A","MA.MSA_height":"ABHD12","MA.Func.region":"","MA.TumorSuppressor":"","MA.Oncogene":"","X":"","X.1":"20p11.21","X.2":"ABD12_HUMAN","X.3":"NP_056415","X.5":"","X.6":"","X.7":""} 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