ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MED MD-021 GAPDH SNP Missense_Mutation 12 6646941 C A 19 44 GBM TCGA-26-5135 GAPDH SNP Missense_Mutation 12 6647098 T G 54 90 LUSC TCGA-33-4566 GAPDH SNP Missense_Mutation 12 6645907 G A 45 100 LUAD TCGA-50-5936 GAPDH SNP Missense_Mutation 12 6647123 G A 42 98 LUSC TCGA-60-2726 GAPDH SNP Missense_Mutation 12 6646779 G T 33 98 BRCA TCGA-A2-A25B GAPDH SNP Missense_Mutation 12 6646882 G C 44 98 UCEC TCGA-A5-A0VP GAPDH SNP Silent 12 6647106 C A 24 65 UCEC TCGA-AP-A0LP GAPDH SNP Missense_Mutation 12 6646115 A G 12 89 UCEC TCGA-B5-A11Y GAPDH SNP Missense_Mutation 12 6646132 G A 40 98 HNSC TCGA-CR-7370 GAPDH SNP Silent 12 6646845 C A 30 98 HNSC TCGA-CV-7421 GAPDH SNP Silent 12 6646508 C T 22 57