ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-191 TMEM82 SNP Missense_Mutation 1 16074123 C G 32 69 ESO ESO-721 TMEM82 SNP Missense_Mutation 1 16073455 G A 38 69 LUAD LUAD-5V8LT TMEM82 SNP Missense_Mutation 1 16069077 C T 22 59 LUAD LUAD-S01302 TMEM82 SNP Missense_Mutation 1 16074087 T A 55 27 MEL ME017 TMEM82 SNP Silent 1 16073486 C T 22 54 MEL ME045 TMEM82 SNP Silent 1 16073396 G A 35 44 MEL MEL-JWCI-WGS-1 TMEM82 SNP Silent 1 16069611 C T 31 50 MEL MEL-JWCI-WGS-1 TMEM82 SNP Missense_Mutation 1 16074047 C T 30 68 MEL MEL-JWCI-WGS-34 TMEM82 DNP Missense_Mutation 1 16069519 CC AA 22 61 MEL MEL-JWCI-WGS-7 TMEM82 SNP Missense_Mutation 1 16069652 C T 30 60 MEL MEL-Ma-Mel-48 TMEM82 SNP Missense_Mutation 1 16074051 C T 30 58 MM MM-0543 TMEM82 SNP Missense_Mutation 1 16070659 C T 30 69 LUSC TCGA-18-3409 TMEM82 SNP Missense_Mutation 1 16074105 C T 30 59 LUSC TCGA-34-5927 TMEM82 SNP Silent 1 16069353 T C 56 81 LUAD TCGA-44-3918 TMEM82 DNP Missense_Mutation 1 16070920 CC AA 22 80 LUAD TCGA-55-1596 TMEM82 SNP Missense_Mutation 1 16069342 C T 26 68 LUAD TCGA-64-5775 TMEM82 SNP Silent 1 16070900 G T 47 74 BRCA TCGA-AN-A0XN TMEM82 SNP Missense_Mutation 1 16069647 G C 36 71 UCEC TCGA-AP-A0LM TMEM82 SNP Missense_Mutation 1 16073439 C A 28 56 BRCA TCGA-AR-A0TX TMEM82 SNP Missense_Mutation 1 16074093 C T 31 58 UCEC TCGA-B5-A0JY TMEM82 SNP Silent 1 16069388 C T 31 65 UCEC TCGA-B5-A0K9 TMEM82 SNP Missense_Mutation 1 16069585 G A 42 52 UCEC TCGA-BS-A0UV TMEM82 SNP Missense_Mutation 1 16069534 G A 37 51 HNSC TCGA-CN-4740 TMEM82 SNP Missense_Mutation 1 16074093 C T 31 58 HNSC TCGA-CV-5441 TMEM82 SNP Missense_Mutation 1 16073407 T C 59 84 UCEC TCGA-D1-A17Q TMEM82 SNP Missense_Mutation 1 16074113 T G 62 48 UCEC TCGA-DI-A0WH TMEM82 SNP Missense_Mutation 1 16069549 C T 31 62 BLCA TCGA-GD-A3OP TMEM82 SNP Missense_Mutation 1 16074093 C T 31 58