ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-160 INA SNP Missense_Mutation 10 105037168 G A 38 55 ESO ESO-191 INA SNP Missense_Mutation 10 105037068 G A 39 61 LUAD LUAD-RT-S01707 INA SNP Missense_Mutation 10 105037083 C G 23 55 LUAD TCGA-17-Z046 INA SNP Missense_Mutation 10 105037801 A G 3 73 LUSC TCGA-18-3409 INA SNP Silent 10 105046812 G A 33 55 LUSC TCGA-18-3409 INA SNP Missense_Mutation 10 105046855 C T 31 72 OV TCGA-23-1022 INA SNP Missense_Mutation 10 105048223 A C 7 88 LUSC TCGA-33-4566 INA SNP Missense_Mutation 10 105036977 C G 31 79 LUSC TCGA-60-2720 INA SNP Silent 10 105037298 G A 33 51 CRC TCGA-A6-2676 INA SNP Missense_Mutation 10 105048220 C A 24 58 CRC TCGA-AA-3977 INA SNP Missense_Mutation 10 105048365 C A 32 69 UCEC TCGA-AX-A0J0 INA SNP Missense_Mutation 10 105037956 C T 27 65 UCEC TCGA-B5-A11E INA SNP Missense_Mutation 10 105046812 G T 33 55 UCEC TCGA-BS-A0TA INA SNP Missense_Mutation 10 105037867 G A 38 97 UCEC TCGA-BS-A0TJ INA SNP Silent 10 105037958 C T 27 50 UCEC TCGA-BS-A0UV INA SNP Nonsense_Mutation 10 105048340 G T 33 86 BLCA TCGA-BT-A2LA INA SNP Missense_Mutation 10 105048262 C T 20 56