ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62854 MNT SNP Nonsense 17 2298527 G A 45 83 LUAD LUAD-CHTN-MAD06-00668 MNT SNP Missense_Mutation 17 2298646 C A 27 71 NB NB-3355 MNT INS Frame_Shift_Ins 17 2298256 - G 55 50 LUAD TCGA-35-3621 MNT SNP Missense_Mutation 17 2290779 C T 19 61 GBM TCGA-41-2571 MNT SNP Missense_Mutation 17 2290511 G A 38 74 LUSC TCGA-85-6175 MNT SNP Missense_Mutation 17 2298341 C A 21 55 UCEC TCGA-A5-A0GW MNT SNP Silent 17 2290573 G A 40 48 CRC TCGA-AA-3715 MNT SNP Silent 17 2290939 A G 6 46 CRC TCGA-AA-3864 MNT SNP Missense_Mutation 17 2290542 C T 27 83 CRC TCGA-AA-3867 MNT SNP Missense_Mutation 17 2290344 C A 23 53 CRC TCGA-AG-A02N MNT SNP Nonsense_Mutation 17 2290266 G A 47 96 UCEC TCGA-AP-A059 MNT SNP Splice_site 17 2297446 C A 24 95 BRCA TCGA-AQ-A1H2 MNT SNP Missense_Mutation 17 2291304 C G 30 93 UCEC TCGA-B5-A0JY MNT SNP Nonsense_Mutation 17 2298206 C A 32 83 UCEC TCGA-B5-A0JY MNT SNP Missense_Mutation 17 2298723 C A 28 60 UCEC TCGA-BG-A0MQ MNT SNP Silent 17 2298309 C T 27 43 HNSC TCGA-CR-6474 MNT SNP Silent 17 2298243 T G 59 48 HNSC TCGA-CV-7095 MNT SNP Missense_Mutation 17 2298449 C T 21 50 HNSC TCGA-CV-7418 MNT SNP Silent 17 2290453 G C 43 85 UCEC TCGA-D1-A103 MNT SNP Silent 17 2290510 C T 23 49 UCEC TCGA-D1-A16F MNT SNP Missense_Mutation 17 2290553 C T 26 70