ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-116 HGS SNP Missense_Mutation 17 79668622 G A 37 82 DLBCL DLBCL-MAYO_DLBCL_234 HGS SNP Missense_Mutation 17 79662951 G A 40 81 HNSC HN_01000 HGS SNP Synonymous 17 79667621 G A 39 51 LUAD TCGA-05-4410 HGS SNP Silent 17 79662893 C T 31 45 GBM TCGA-19-1790 HGS SNP Nonsense_Mutation 17 79668638 C A 29 61 OV TCGA-24-1417 HGS SNP Silent 17 79653372 G A 33 53 OV TCGA-25-1326 HGS SNP Missense 17 79662057 A T 7 52 LUSC TCGA-34-5236 HGS SNP Missense_Mutation 17 79668078 C T 32 60 LUSC TCGA-39-5031 HGS SNP Missense_Mutation 17 79658588 G C 37 89 LUSC TCGA-66-2787 HGS SNP Missense_Mutation 17 79667556 C T 22 64 UCEC TCGA-AP-A051 HGS SNP Missense_Mutation 17 79662041 A G 10 53 UCEC TCGA-AP-A054 HGS SNP Missense_Mutation 17 79663641 A G 14 73 UCEC TCGA-AP-A059 HGS SNP Silent 17 79653396 C T 19 44 UCEC TCGA-AP-A059 HGS SNP Missense_Mutation 17 79658493 G A 48 91 UCEC TCGA-AP-A0LM HGS SNP Missense_Mutation 17 79657241 G A 37 95 UCEC TCGA-B5-A0K7 HGS SNP Silent 17 79655784 C T 24 56 UCEC TCGA-B5-A11E HGS SNP Missense_Mutation 17 79663463 G T 34 58 UCEC TCGA-B5-A11J HGS SNP Silent 17 79654056 C T 20 73 UCEC TCGA-B5-A11R HGS SNP Missense_Mutation 17 79660922 C T 31 54 BRCA TCGA-B6-A0RL HGS SNP Missense_Mutation 17 79663674 G A 38 80 KIRC TCGA-BP-4972 HGS SNP Missense_Mutation 17 79667601 T C 53 84 UCEC TCGA-BS-A0UA HGS SNP Missense_Mutation 17 79663956 A G 4 71 BRCA TCGA-C8-A137 HGS SNP Missense_Mutation 17 79653400 G T 38 93 BRCA TCGA-C8-A1HM HGS SNP Missense_Mutation 17 79661866 G A 45 90 HNSC TCGA-CR-7364 HGS SNP Missense_Mutation 17 79662939 A G 5 86 HNSC TCGA-CR-7379 HGS SNP Silent 17 79658578 G A 34 76 HNSC TCGA-CR-7386 HGS SNP Silent 17 79663007 C T 29 95 HNSC TCGA-CV-6441 HGS SNP Silent 17 79667588 C T 23 45 KIRC TCGA-CZ-5457 HGS SNP Missense_Mutation 17 79652641 C T 27 95 UCEC TCGA-D1-A103 HGS SNP Missense_Mutation 17 79663480 G A 38 91 UCEC TCGA-D1-A17F HGS SNP Silent 17 79667588 C T 23 45 UCEC TCGA-D1-A17Q HGS SNP Silent 17 79668134 C T 31 49 BRCA TCGA-D8-A27K HGS SNP Missense_Mutation 17 79662012 G A 34 81 BLCA TCGA-DK-A1AF HGS SNP Splice_Site 17 79660899 G T 33 87 BRCA TCGA-E2-A10B HGS SNP Silent 17 79662007 C T 25 33 BLCA TCGA-G2-A2ES HGS SNP Silent 17 79668080 C T 29 56