ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-B02477 CHRND SNP Silent 2 233394675 C A 23 57 LUAD LUAD-F00089 CHRND SNP Missense_Mutation 2 233390953 C A 28 77 LUAD LUAD-RT-S01721 CHRND SNP Silent 2 233394797 C A 24 60 LUAD LUAD-S01315 CHRND SNP Missense_Mutation 2 233391358 C A 24 58 MM MM-0421-FIX CHRND SNP Missense 2 233398753 C T 26 99 RHAB Rhabdoid-09-044 CHRND SNP Missense_Mutation 2 233398961 C A 26 55 LUAD TCGA-05-4396 CHRND SNP Silent 2 233396325 C A 23 70 LUAD TCGA-05-4418 CHRND SNP Missense_Mutation 2 233398943 C A 21 83 LUAD TCGA-05-4420 CHRND SNP Missense_Mutation 2 233392136 C A 18 91 LUAD TCGA-05-4432 CHRND SNP Missense_Mutation 2 233399022 C A 18 52 GBM TCGA-06-2570 CHRND SNP Missense_Mutation 2 233392979 C A 17 53 OV TCGA-13-0730 CHRND SNP Nonsense_Mutation 2 233393271 C A 31 33 GBM TCGA-16-1048 CHRND SNP Missense_Mutation 2 233394760 G A 38 100 LUAD TCGA-17-Z015 CHRND SNP Missense_Mutation 2 233394818 G T 47 69 LUAD TCGA-17-Z055 CHRND SNP Missense_Mutation 2 233396169 G A 39 89 GBM TCGA-19-2631 CHRND SNP Missense_Mutation 2 233394744 T C 53 78 OV TCGA-25-1634 CHRND SNP Missense_Mutation 2 233394757 G A 38 72 LUSC TCGA-33-4566 CHRND SNP Missense_Mutation 2 233396137 T A 55 81 LUAD TCGA-35-3621 CHRND SNP Missense_Mutation 2 233394711 C G 32 57 LUAD TCGA-38-4632 CHRND SNP Splice_Site 2 233396061 G A 35 98 LUAD TCGA-44-3918 CHRND SNP Missense_Mutation 2 233392133 C A 20 78 LUAD TCGA-44-3918 CHRND SNP Missense_Mutation 2 233398732 C T 30 87 LUAD TCGA-50-5049 CHRND SNP Nonsense_Mutation 2 233398755 G T 37 100 LUSC TCGA-60-2724 CHRND SNP Silent 2 233390970 G T 39 40 LUAD TCGA-64-5778 CHRND SNP Nonsense_Mutation 2 233391331 G T 33 84 LUSC TCGA-66-2759 CHRND SNP Silent 2 233390967 G A 47 65 LUSC TCGA-66-2785 CHRND SNP Missense_Mutation 2 233393325 C G 24 67 LUAD TCGA-75-6211 CHRND SNP Missense_Mutation 2 233391241 A T 7 52 BRCA TCGA-A2-A0SW CHRND SNP Missense_Mutation 2 233399897 G T 44 62 UCEC TCGA-A5-A0VQ CHRND SNP Missense_Mutation 2 233393243 G A 46 66 CRC TCGA-AA-3949 CHRND SNP Missense_Mutation 2 233400011 C T 27 88 CRC TCGA-AA-3977 CHRND SNP Silent 2 233398974 C A 32 48 CRC TCGA-AA-A00J CHRND SNP Missense_Mutation 2 233398757 G T 35 79 CRC TCGA-AA-A00N CHRND SNP Missense_Mutation 2 233393337 C T 31 53 UCEC TCGA-AP-A059 CHRND SNP Missense_Mutation 2 233391346 G A 40 46 UCEC TCGA-AP-A0LT CHRND SNP Missense_Mutation 2 233399886 G A 46 67 UCEC TCGA-B5-A11E CHRND SNP Missense_Mutation 2 233394809 C T 32 71 HNSC TCGA-BA-4078 CHRND SNP Missense_Mutation 2 233394727 G T 38 51 BRCA TCGA-BH-A1F8 CHRND SNP Missense_Mutation 2 233399028 G A 45 76 HNSC TCGA-CQ-6228 CHRND SNP Missense_Mutation 2 233399048 A C 4 78 HNSC TCGA-CR-7367 CHRND SNP Missense_Mutation 2 233398936 C T 23 50 HNSC TCGA-CR-7385 CHRND SNP Missense_Mutation 2 233393036 T C 54 86 UCEC TCGA-D1-A167 CHRND SNP Missense_Mutation 2 233393033 G A 38 94 BRCA TCGA-E2-A15I CHRND DEL Frame_Shift_Del 2 233399890 G - 48 52