ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-1427 INTS4 SNP Missense_Mutation 11 77639529 C A 32 54 ESO ESO-161 INTS4 SNP Missense_Mutation 11 77632480 G T 44 57 HNSC HN_62686 INTS4 SNP Missense 11 77602822 G A 42 94 LUAD LUAD-CHTN-MAD06-00668 INTS4 SNP Missense_Mutation 11 77649813 C A 20 77 LUAD LUAD-E00443 INTS4 SNP Missense_Mutation 11 77690098 T A 59 75 LUAD LUAD-RT-S01721 INTS4 SNP Missense_Mutation 11 77702190 C A 24 66 LUAD LUAD_E00623 INTS4 SNP Missense_Mutation 11 77635857 C A 25 94 MEL ME001 INTS4 SNP Silent 11 77635822 G A 44 55 MEL ME049 INTS4 SNP Missense_Mutation 11 77702192 C T 32 97 MEL MEL-JWCI-14 INTS4 SNP Nonsense_Mutation 11 77667005 G A 45 76 MEL MEL-JWCI-WGS-35 INTS4 SNP Missense_Mutation 11 77618789 G A 33 93 MM MM-0343 INTS4 SNP Missense 11 77594925 C A 23 85 MM MM-0439_2 INTS4 SNP Silent 11 77639439 G A 48 54 PRAD PR-02-2072 INTS4 SNP Splice_Site_SNP 11 77669791 C T 18 95 PRAD PR-09-5245 INTS4 SNP Silent 11 77618847 T C 64 51 PRAD PR-P559 INTS4 SNP Missense_Mutation 11 77690046 C T 25 81 OV TCGA-04-1343 INTS4 SNP Silent 11 77672104 G C 45 49 LUAD TCGA-05-4382 INTS4 DNP Missense_Mutation 11 77671418 CC AA 30 70 LUAD TCGA-05-4396 INTS4 SNP Missense_Mutation 11 77649766 C A 23 69 LUAD TCGA-05-4396 INTS4 SNP Missense_Mutation 11 77705667 C A 23 97 GBM TCGA-06-0650 INTS4 SNP Missense_Mutation 11 77632412 G C 33 84 LUAD TCGA-17-Z026 INTS4 SNP Nonsense_Mutation 11 77635798 C T 30 94 LUAD TCGA-17-Z031 INTS4 SNP Missense_Mutation 11 77635818 T C 57 87 LUSC TCGA-18-3416 INTS4 SNP Nonsense_Mutation 11 77705659 C A 29 97 OV TCGA-20-0991 INTS4 SNP Silent 11 77639496 G A 40 58 LUAD TCGA-44-3919 INTS4 SNP Nonsense_Mutation 11 77618831 G A 45 92 LUAD TCGA-50-6597 INTS4 SNP Missense_Mutation 11 77649800 C A 22 92 CRC TCGA-AA-3525 INTS4 SNP Missense_Mutation 11 77590170 G A 46 97 CRC TCGA-AA-3672 INTS4 SNP Missense_Mutation 11 77602456 G T 35 100 AML TCGA-AB-2828 INTS4 SNP Silent 11 77590088 C T 32 53 CRC TCGA-AG-3883 INTS4 SNP Missense_Mutation 11 77612476 G A 36 77 UCEC TCGA-AP-A054 INTS4 SNP Silent 11 77605371 A G 6 62 UCEC TCGA-AP-A056 INTS4 SNP Missense_Mutation 11 77633494 C T 23 95 UCEC TCGA-AP-A059 INTS4 SNP Missense_Mutation 11 77602750 G T 33 55 UCEC TCGA-AP-A0LM INTS4 SNP Missense_Mutation 11 77590056 C T 26 98 UCEC TCGA-AP-A0LP INTS4 SNP Silent 11 77594924 C T 26 44 UCEC TCGA-B5-A0JY INTS4 SNP Missense_Mutation 11 77602451 G A 38 51 BRCA TCGA-BH-A0E9 INTS4 INS Frame_Shift_Ins 11 77702264 - T 28 97 BRCA TCGA-BH-A0HA INTS4 SNP Silent 11 77618841 A G 5 60 HNSC TCGA-CV-5970 INTS4 SNP Missense_Mutation 11 77590009 G C 44 98 BRCA TCGA-E9-A295 INTS4 SNP Silent 11 77702202 C T 23 48 BLCA TCGA-FD-A3NA INTS4 SNP Missense_Mutation 11 77669853 C T 29 81 BLCA TCGA-GD-A2C5 INTS4 SNP Nonsense_Mutation 11 77629999 G C 45 92 BLCA TCGA-H4-A2HO INTS4 SNP Missense_Mutation 11 77605369 T G 62 89