ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0061 ZC3H12C SNP Missense_Mutation 11 110036329 A C 3 69 ESO ESO-512 ZC3H12C SNP Missense_Mutation 11 110035499 G A 45 56 ESO ESO-512 ZC3H12C SNP Missense_Mutation 11 110036067 G A 45 98 HNSC HN_63021 ZC3H12C SNP Missense 11 110036071 C A 32 99 LUAD LUAD-B01246 ZC3H12C SNP Nonsense_Mutation 11 110035779 G T 33 85 LUAD LUAD-B01811 ZC3H12C SNP Missense_Mutation 11 110007586 G T 43 51 LUAD LUAD-RT-S01721 ZC3H12C SNP Missense_Mutation 11 110007655 G A 45 80 MEL MEL-JWCI-WGS-38 ZC3H12C SNP Missense_Mutation 11 110007635 C T 32 67 MEL MEL-Ma-Mel-108 ZC3H12C DNP Missense_Mutation 11 110036167 CC TT 26 68 MEL MEL-UKRV-Mel-6 ZC3H12C SNP Missense_Mutation 11 110035834 C T 23 98 LUAD TCGA-05-4396 ZC3H12C SNP Missense_Mutation 11 110035818 C A 23 99 LUAD TCGA-05-4396 ZC3H12C SNP Missense_Mutation 11 110036118 C A 23 58 LUAD TCGA-05-4432 ZC3H12C SNP Nonsense_Mutation 11 110023681 A T 1 78 LUSC TCGA-18-3419 ZC3H12C SNP Missense_Mutation 11 110036441 G T 33 75 LUSC TCGA-34-2596 ZC3H12C SNP Missense_Mutation 11 110035605 C A 32 63 LUAD TCGA-35-3615 ZC3H12C SNP Silent 11 110007729 C T 25 54 LUAD TCGA-44-3918 ZC3H12C SNP Missense_Mutation 11 110023660 G T 36 85 LUAD TCGA-44-3918 ZC3H12C SNP Missense_Mutation 11 110036179 G C 39 80 LUAD TCGA-49-6743 ZC3H12C SNP Missense_Mutation 11 110035917 C T 32 50 LUAD TCGA-55-1592 ZC3H12C SNP Missense_Mutation 11 110035851 C T 21 86 LUAD TCGA-55-6642 ZC3H12C SNP Missense_Mutation 11 110035384 C T 21 91 LUSC TCGA-66-2789 ZC3H12C SNP Missense_Mutation 11 110034020 C A 32 69 LUSC TCGA-70-6723 ZC3H12C SNP Missense_Mutation 11 110036409 G A 38 59 BRCA TCGA-A2-A0CL ZC3H12C SNP Missense_Mutation 11 110035921 C T 23 85 UCEC TCGA-A5-A0VQ ZC3H12C SNP Silent 11 110036165 C T 19 39 BRCA TCGA-A8-A08R ZC3H12C SNP Missense_Mutation 11 110035764 C T 22 63 CRC TCGA-AA-3672 ZC3H12C SNP Missense_Mutation 11 110036419 T G 54 91 CRC TCGA-AA-3679 ZC3H12C SNP Missense_Mutation 11 110007605 C T 27 63 CRC TCGA-AA-3715 ZC3H12C SNP Silent 11 110036357 C T 30 85 CRC TCGA-AA-3811 ZC3H12C SNP Missense_Mutation 11 110035819 G A 38 72 CRC TCGA-AA-3966 ZC3H12C SNP Missense_Mutation 11 110036424 G A 38 99 CRC TCGA-AA-3977 ZC3H12C SNP Nonsense_Mutation 11 110023657 G T 33 99 CRC TCGA-AA-3984 ZC3H12C SNP Nonsense_Mutation 11 110023657 G T 33 99 CRC TCGA-AA-A00N ZC3H12C SNP Missense_Mutation 11 110007877 A G 13 89 CRC TCGA-AA-A010 ZC3H12C SNP Missense_Mutation 11 110007398 T G 59 59 CRC TCGA-AG-A002 ZC3H12C SNP Missense_Mutation 11 110035566 G A 37 88 CRC TCGA-AG-A002 ZC3H12C SNP Missense_Mutation 11 110036163 G A 37 79 UCEC TCGA-AP-A056 ZC3H12C SNP Missense_Mutation 11 110035666 T C 49 87 UCEC TCGA-AP-A059 ZC3H12C SNP Missense_Mutation 11 110035530 C A 26 64 UCEC TCGA-AP-A0LM ZC3H12C SNP Missense_Mutation 11 110007499 C A 24 85 UCEC TCGA-AP-A0LM ZC3H12C SNP Silent 11 110035730 C T 19 36 UCEC TCGA-AP-A0LM ZC3H12C SNP Missense_Mutation 11 110035954 T G 59 69 UCEC TCGA-AP-A0LT ZC3H12C SNP Missense_Mutation 11 110035624 G A 37 66 KIRC TCGA-B2-4101 ZC3H12C SNP Silent 11 110035964 G A 44 50 UCEC TCGA-B5-A0JY ZC3H12C SNP Nonsense_Mutation 11 110023657 G T 33 99 UCEC TCGA-B5-A0JY ZC3H12C SNP Missense_Mutation 11 110030212 A G 10 91 UCEC TCGA-B5-A0K9 ZC3H12C SNP Silent 11 110023767 T C 55 47 UCEC TCGA-B5-A11R ZC3H12C SNP Missense_Mutation 11 110030004 G C 33 99 UCEC TCGA-B5-A11R ZC3H12C SNP Missense_Mutation 11 110030100 G C 45 98 BRCA TCGA-BH-A0BZ ZC3H12C SNP Missense_Mutation 11 110034079 A C 2 51 BRCA TCGA-BH-A203 ZC3H12C SNP Nonsense_Mutation 11 110030002 T A 61 90 UCEC TCGA-BS-A0UV ZC3H12C SNP Silent 11 110007471 G A 35 72 UCEC TCGA-BS-A0UV ZC3H12C SNP Missense_Mutation 11 110030104 C T 31 98 BLCA TCGA-BT-A20T ZC3H12C SNP Missense_Mutation 11 110035800 C A 17 84 HNSC TCGA-CR-6478 ZC3H12C SNP Missense_Mutation 11 110036199 G A 37 66 HNSC TCGA-CV-6961 ZC3H12C SNP Missense_Mutation 11 110023720 G C 33 99 HNSC TCGA-CV-7178 ZC3H12C SNP Missense_Mutation 11 110035195 G A 41 68 UCEC TCGA-D1-A103 ZC3H12C SNP Missense_Mutation 11 110007838 G A 48 72 UCEC TCGA-D1-A167 ZC3H12C SNP Missense_Mutation 11 110007998 C T 19 73 UCEC TCGA-D1-A177 ZC3H12C SNP Missense_Mutation 11 110036032 G T 35 65