ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62421 NMT2 SNP Splice_Site_SNP 10 15151839 C T 32 100 HNSC HN_63021 NMT2 SNP Synonymous 10 15161372 C T 22 67 LUAD LUAD_E00565 NMT2 SNP Missense_Mutation 10 15170395 C A 32 100 MEL MEL-JWCI-WGS-12 NMT2 SNP Silent 10 15175114 C T 32 67 MEL MEL-JWCI-WGS-12 NMT2 SNP Missense_Mutation 10 15175251 G A 42 79 MM MM-0465 NMT2 SNP Missense_Mutation 10 15175345 G A 45 88 LUAD TCGA-05-4396 NMT2 SNP Silent 10 15172176 C G 23 25 LUAD TCGA-05-4396 NMT2 SNP Missense_Mutation 10 15174859 C A 23 100 GBM TCGA-14-4157 NMT2 SNP Missense_Mutation 10 15183429 G A 42 70 OV TCGA-23-1021 NMT2 SNP Missense_Mutation 10 15161468 G C 45 51 LUSC TCGA-51-4081 NMT2 SNP Missense_Mutation 10 15154953 C T 23 98 LUAD TCGA-67-3771 NMT2 SNP Missense_Mutation 10 15210517 G C 40 57 BRCA TCGA-A2-A0YM NMT2 SNP Nonsense_Mutation 10 15151734 G T 48 78 KIRC TCGA-A3-3378 NMT2 DEL Frame_Shift_Del 10 15151779 T - 60 72 CRC TCGA-A6-2676 NMT2 SNP Missense_Mutation 10 15170359 C A 32 100 CRC TCGA-AA-A00N NMT2 SNP Missense_Mutation 10 15170395 C A 32 100 CRC TCGA-AA-A00N NMT2 SNP Nonsense_Mutation 10 15183425 G A 37 87 UCEC TCGA-AP-A051 NMT2 SNP Silent 10 15154819 G A 38 47 UCEC TCGA-AP-A051 NMT2 SNP Missense_Mutation 10 15177311 C A 32 75 UCEC TCGA-AP-A0LM NMT2 SNP Silent 10 15154813 C T 27 40 UCEC TCGA-AP-A0LM NMT2 SNP Missense_Mutation 10 15161391 G A 42 86 UCEC TCGA-B5-A0JY NMT2 SNP Nonsense_Mutation 10 15161458 G A 37 67 KIRC TCGA-B8-5158 NMT2 SNP Missense_Mutation 10 15154856 T C 60 79 KIRC TCGA-BP-5186 NMT2 SNP Missense_Mutation 10 15151770 A T 5 65 KIRC TCGA-CJ-4882 NMT2 SNP Splice_site 10 15161511 A T 2 55 HNSC TCGA-CN-5364 NMT2 SNP Missense_Mutation 10 15175327 C G 32 100 HNSC TCGA-CV-6933 NMT2 SNP Missense_Mutation 10 15151773 C G 20 79 UCEC TCGA-D1-A103 NMT2 SNP Missense_Mutation 10 15172258 G A 37 88 UCEC TCGA-D1-A17D NMT2 SNP Missense_Mutation 10 15172253 G A 40 87 BLCA TCGA-DK-A2I4 NMT2 SNP Missense_Mutation 10 15175327 C G 32 100 BRCA TCGA-EW-A1P4 NMT2 SNP Missense_Mutation 10 15161504 C G 32 65 BLCA TCGA-G2-A2EF NMT2 SNP Missense_Mutation 10 15174885 C G 32 100