ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-085 FAM126A SNP Missense_Mutation 7 23017004 T C 54 68 LUAD LUAD-5V8LT FAM126A SNP Silent 7 23004075 T C 55 48 LUAD LUAD-TJW61 FAM126A SNP Missense_Mutation 7 23015917 C A 20 100 MEL MEL-JWCI-WGS-32 FAM126A SNP Silent 7 23017963 G A 44 68 MEL MEL-Ma-Mel-85 FAM126A SNP Silent 7 22985415 G A 35 53 MM MM-0535 FAM126A SNP Missense_Mutation 7 22985559 A C 5 49 LUAD TCGA-05-4396 FAM126A SNP Silent 7 22985688 C A 23 45 LUAD TCGA-05-4396 FAM126A SNP Splice_site 7 22999875 C A 21 96 GBM TCGA-27-2519 FAM126A SNP Missense_Mutation 7 22985627 G A 40 68 GBM TCGA-27-2523 FAM126A SNP Nonsense_Mutation 7 23023600 G T 45 100 LUAD TCGA-38-4631 FAM126A SNP Missense_Mutation 7 22999980 C T 30 82 LUSC TCGA-46-6026 FAM126A SNP Missense_Mutation 7 23018024 C A 20 100 LUAD TCGA-50-5049 FAM126A SNP Silent 7 22985289 T A 55 44 LUSC TCGA-66-2785 FAM126A SNP Missense_Mutation 7 23030703 C G 30 85 LUAD TCGA-91-6836 FAM126A SNP Missense_Mutation 7 23000883 G T 47 95 CRC TCGA-AA-3562 FAM126A SNP Missense_Mutation 7 22985434 G A 38 78 CRC TCGA-AA-3855 FAM126A SNP Missense_Mutation 7 22985641 C T 30 92 CRC TCGA-AA-3947 FAM126A SNP Missense_Mutation 7 23017931 C T 28 71 CRC TCGA-AA-A00N FAM126A SNP Silent 7 22985253 A G 10 49 CRC TCGA-AA-A010 FAM126A SNP Missense_Mutation 7 23023638 A C 4 64 CRC TCGA-AA-A01Q FAM126A SNP Missense_Mutation 7 22985354 C T 26 37 CRC TCGA-AG-A002 FAM126A SNP Nonsense_Mutation 7 23000877 C A 32 95 UCEC TCGA-AX-A05Z FAM126A SNP Silent 7 23015832 G A 45 100 KIRC TCGA-B0-5706 FAM126A DEL Frame_Shift_Del 7 23000857 CA - 25 52 UCEC TCGA-B5-A0JY FAM126A SNP Splice_Site 7 23016959 C A 20 100 UCEC TCGA-B5-A0JY FAM126A SNP Missense_Mutation 7 23030716 C A 32 50 UCEC TCGA-BS-A0UF FAM126A SNP Silent 7 22999924 T C 62 55 BLCA TCGA-BT-A20W FAM126A SNP Missense_Mutation 7 23016375 C A 18 72 BLCA TCGA-CU-A0YR FAM126A SNP Silent 7 22985595 T C 64 48 UCEC TCGA-D1-A0ZO FAM126A SNP Missense_Mutation 7 23030705 A G 6 79 UCEC TCGA-D1-A16X FAM126A SNP Nonsense_Mutation 7 22985597 C A 32 92 UCEC TCGA-D1-A16Y FAM126A SNP Nonsense_Mutation 7 22985591 C A 32 92 BRCA TCGA-D8-A1XV FAM126A SNP Silent 7 22985376 C T 19 49 UCEC TCGA-DI-A0WH FAM126A SNP Missense_Mutation 7 22985626 C T 23 79 BLCA TCGA-H4-A2HQ FAM126A SNP Missense_Mutation 7 23030703 C T 30 85