ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-Ls843 FAM196A SNP Missense_Mutation 10 128974589 A G 7 61 DLBCL DLBCL-MAYO_DLBCL_234 FAM196A SNP Missense_Mutation 10 128973917 A G 6 73 HNSC HN_62861 FAM196A SNP Missense 10 128974153 C G 32 58 LUAD LUAD-B00731 FAM196A SNP Missense_Mutation 10 128973556 C G 29 55 LUAD LUAD-B02050 FAM196A SNP Missense_Mutation 10 128973866 G T 42 58 LUAD LUAD-LC15C FAM196A SNP Missense_Mutation 10 128974022 G C 36 67 MEL MEL-Ma-Mel-48 FAM196A SNP Missense_Mutation 10 128973797 C T 23 40 LUAD TCGA-05-4396 FAM196A SNP Nonsense_Mutation 10 128936127 C A 23 84 LUAD TCGA-05-4396 FAM196A SNP Silent 10 128936161 G T 47 62 LUAD TCGA-05-4396 FAM196A SNP Silent 10 128974429 G T 39 47 LUAD TCGA-05-4426 FAM196A SNP Missense_Mutation 10 128974461 C A 22 63 GBM TCGA-06-0648 FAM196A SNP Silent 10 128973691 C T 27 50 LUAD TCGA-17-Z056 FAM196A SNP Missense_Mutation 10 128974376 G T 41 96 LUSC TCGA-18-3409 FAM196A SNP Silent 10 128974270 G A 41 53 LUSC TCGA-18-4083 FAM196A SNP Nonsense_Mutation 10 128936119 C T 30 98 LUSC TCGA-22-1016 FAM196A SNP Missense_Mutation 10 128974520 A T 6 89 OV TCGA-24-1556 FAM196A SNP Nonsense_Mutation 10 128974315 G T 44 82 OV TCGA-25-1319 FAM196A SNP Missense_Mutation 10 128974383 G A 40 80 LUSC TCGA-39-5021 FAM196A SNP Silent 10 128973697 C T 28 68 LUSC TCGA-43-6771 FAM196A SNP Silent 10 128973730 C G 31 50 LUAD TCGA-44-2655 FAM196A SNP Missense_Mutation 10 128973999 C A 31 56 LUAD TCGA-44-2657 FAM196A SNP Missense_Mutation 10 128973656 G C 35 66 LUAD TCGA-50-5933 FAM196A SNP Silent 10 128974033 G C 41 53 GBM TCGA-76-4928 FAM196A SNP Nonsense_Mutation 10 128974485 G A 46 97 LUAD TCGA-86-6562 FAM196A SNP Splice_site 10 128936283 C A 17 83 BRCA TCGA-A2-A0CX FAM196A SNP Nonsense_Mutation 10 128974473 G A 48 85 UCEC TCGA-A5-A0VP FAM196A SNP Silent 10 128973601 C T 23 39 CRC TCGA-AA-3542 FAM196A SNP Missense_Mutation 10 128936219 A G 4 69 CRC TCGA-AA-3864 FAM196A SNP Missense_Mutation 10 128974365 C T 19 96 CRC TCGA-AA-3982 FAM196A INS Frame_Shift_Ins 10 128973936 - TA 41 61 CRC TCGA-AA-A00N FAM196A SNP Splice_site 10 128952186 G A 34 90 CRC TCGA-AG-A002 FAM196A SNP Silent 10 128973613 G A 37 46 CRC TCGA-AG-A026 FAM196A SNP Missense_Mutation 10 128973764 G A 38 50 BRCA TCGA-AO-A0JL FAM196A SNP Missense_Mutation 10 128973678 G C 43 49 UCEC TCGA-AP-A059 FAM196A SNP Missense_Mutation 10 128974260 C A 32 92 UCEC TCGA-AP-A0LM FAM196A SNP Silent 10 128973940 G A 39 42 UCEC TCGA-AX-A05Z FAM196A SNP Missense_Mutation 10 128974463 G A 37 72 UCEC TCGA-AX-A0J0 FAM196A SNP Missense_Mutation 10 128973653 C A 20 81 UCEC TCGA-AX-A0J0 FAM196A SNP Missense_Mutation 10 128974003 C A 28 55 UCEC TCGA-B5-A11E FAM196A SNP Missense_Mutation 10 128952149 T A 58 69 UCEC TCGA-B5-A11E FAM196A SNP Silent 10 128974189 C T 24 51 UCEC TCGA-B5-A11E FAM196A SNP Missense_Mutation 10 128974626 T C 59 51 HNSC TCGA-BA-4078 FAM196A SNP Nonsense_Mutation 10 128974408 G T 44 43 UCEC TCGA-BS-A0UV FAM196A SNP Nonsense_Mutation 10 128973618 G A 40 82 UCEC TCGA-BS-A0UV FAM196A SNP Missense_Mutation 10 128974518 G A 38 66 KIRC TCGA-CJ-6030 FAM196A SNP Missense_Mutation 10 128974169 G A 38 72 HNSC TCGA-CN-4734 FAM196A SNP Nonsense_Mutation 10 128974488 C A 29 97 HNSC TCGA-CN-5360 FAM196A SNP Silent 10 128974171 G C 38 22 UCEC TCGA-D1-A103 FAM196A SNP Missense_Mutation 10 128973774 C T 23 96 UCEC TCGA-D1-A167 FAM196A SNP Missense_Mutation 10 128974596 C T 27 66 UCEC TCGA-D1-A174 FAM196A SNP Missense_Mutation 10 128973602 G A 40 67 UCEC TCGA-D1-A174 FAM196A SNP Missense_Mutation 10 128973720 G T 35 68