ttype patient gene classification type chr pos ref_allele newbase context65 cons46 GBM TCGA-06-0939 MED7 SNP Missense_Mutation 5 156565766 A G 4 77 LUAD TCGA-17-Z021 MED7 SNP Silent 5 156566062 T A 58 58 LUAD TCGA-17-Z026 MED7 SNP Missense_Mutation 5 156565908 C G 32 85 GBM TCGA-19-2625 MED7 SNP Missense_Mutation 5 156566183 A G 4 80 GBM TCGA-32-2498 MED7 SNP Missense_Mutation 5 156566376 C A 30 87 LUSC TCGA-39-5030 MED7 SNP Missense_Mutation 5 156565862 C A 28 63 LUAD TCGA-44-6778 MED7 SNP Silent 5 156565909 T C 55 36 LUSC TCGA-66-2758 MED7 SNP Missense_Mutation 5 156566273 C G 27 88 BRCA TCGA-A8-A090 MED7 SNP Nonsense_Mutation 5 156566070 C A 29 100 CRC TCGA-AG-A002 MED7 SNP Missense_Mutation 5 156566122 C A 32 63 UCEC TCGA-AP-A059 MED7 SNP Silent 5 156565792 C T 32 51 BRCA TCGA-AR-A24H MED7 SNP Missense_Mutation 5 156565934 G C 33 100 UCEC TCGA-AX-A0J1 MED7 SNP Missense_Mutation 5 156566061 G A 44 100 KIRC TCGA-B0-5115 MED7 SNP Missense_Mutation 5 156565914 G T 45 85 UCEC TCGA-B5-A0JY MED7 SNP Missense_Mutation 5 156566386 C A 24 56 UCEC TCGA-B5-A11E MED7 SNP Silent 5 156566251 G A 37 49 UCEC TCGA-BS-A0UV MED7 SNP Missense_Mutation 5 156565988 C A 32 100 BLCA TCGA-CF-A1HS MED7 SNP Missense_Mutation 5 156565803 G C 45 81 HNSC TCGA-CR-7388 MED7 SNP Missense_Mutation 5 156566373 C T 29 100