ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-041 NMT1 SNP Nonsense_Mutation 17 43159088 G T 45 68 DLBCL DLBCL-MAYO_DLBCL_234 NMT1 SNP Missense_Mutation 17 43181080 G A 38 52 MEL MEL-JWCI-14 NMT1 SNP Missense_Mutation 17 43181174 C T 32 100 MEL MEL-JWCI-WGS-11 NMT1 SNP Silent 17 43176824 C T 22 58 LUAD TCGA-05-4384 NMT1 DNP Missense_Mutation 17 43175845 GG TT 39 100 LUAD TCGA-50-5946 NMT1 SNP Missense_Mutation 17 43159018 G C 45 62 UCEC TCGA-A5-A0G9 NMT1 SNP Missense_Mutation 17 43182276 T A 62 93 BRCA TCGA-A8-A08H NMT1 SNP Missense_Mutation 17 43163979 G A 37 100 CRC TCGA-AA-A01R NMT1 SNP Nonsense_Mutation 17 43180340 C T 27 64 UCEC TCGA-AP-A059 NMT1 SNP Missense_Mutation 17 43173623 G A 37 100 BRCA TCGA-AR-A0U3 NMT1 SNP Nonsense_Mutation 17 43183002 C T 17 88 UCEC TCGA-AX-A0J0 NMT1 SNP Silent 17 43180480 C T 31 48 UCEC TCGA-AX-A0J1 NMT1 SNP Splice_site 17 43171054 C T 27 49 UCEC TCGA-BG-A0VW NMT1 DEL Frame_Shift_Del 17 43175900 A - 5 58 KIRC TCGA-CJ-5675 NMT1 SNP Missense_Mutation 17 43173564 A C 13 56 HNSC TCGA-CR-6481 NMT1 SNP Silent 17 43171126 C G 22 54 HNSC TCGA-CR-7385 NMT1 SNP Missense_Mutation 17 43175832 G C 33 100 HNSC TCGA-CV-6441 NMT1 SNP Missense_Mutation 17 43159057 G C 33 81 HNSC TCGA-CV-7415 NMT1 SNP Missense_Mutation 17 43175850 C T 29 81 HNSC TCGA-CV-7427 NMT1 SNP Missense_Mutation 17 43159088 G A 45 68 HNSC TCGA-CV-7427 NMT1 SNP Silent 17 43159090 G A 33 51 BLCA TCGA-H4-A2HQ NMT1 SNP Missense_Mutation 17 43138785 T C 55 80 HNSC TCGA-HD-7229 NMT1 SNP Missense_Mutation 17 43180413 C T 19 73