ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-079 C1R SNP Silent 12 7188021 G A 33 49 BRCA BR-MEX-191 C1R SNP Missense_Mutation 12 7188474 C T 31 99 CLL CW224 C1R SNP Missense_Mutation 12 7241530 G T 43 56 ESO ESO-S41 C1R SNP Missense_Mutation 12 7187930 G A 41 77 LUAD LUAD-S01345 C1R SNP Missense_Mutation 12 7188009 C T 27 52 MEL ME009 C1R SNP Missense_Mutation 12 7242222 G A 41 54 MEL ME009 C1R SNP Silent 12 7244165 G A 44 60 MEL ME010 C1R SNP Missense_Mutation 12 7241972 C T 22 79 MEL MEL-Ma-Mel-54a C1R SNP Missense_Mutation 12 7188438 G A 41 64 MEL MEL-Ma-Mel-85 C1R SNP Nonsense_Mutation 12 7242772 T A 64 51 MM MM-0562 C1R SNP Silent 12 7188271 C T 21 47 LUAD TCGA-05-5715 C1R SNP Missense_Mutation 12 7188187 C G 29 56 LUAD TCGA-17-Z026 C1R SNP Silent 12 7242749 C A 30 46 LUSC TCGA-21-1070 C1R SNP Silent 12 7241892 T A 57 43 LUAD TCGA-50-5066 C1R SNP Silent 12 7188193 C A 21 41 LUSC TCGA-60-2708 C1R SNP Missense_Mutation 12 7241522 C T 31 80 LUSC TCGA-66-2771 C1R SNP Missense_Mutation 12 7187907 C A 22 71 LUSC TCGA-66-2789 C1R SNP Missense_Mutation 12 7187955 G A 37 68 CRC TCGA-AA-3715 C1R SNP Silent 12 7188559 G A 37 41 CRC TCGA-AA-3821 C1R DEL Frame_Shift_Del 12 7242010 G - 35 67 CRC TCGA-AA-3984 C1R SNP Missense_Mutation 12 7242716 G T 33 78 CRC TCGA-AG-A002 C1R SNP Missense_Mutation 12 7188279 C T 27 100 UCEC TCGA-AP-A051 C1R SNP Missense_Mutation 12 7241941 G T 35 69 UCEC TCGA-AP-A0LM C1R SNP Silent 12 7241269 C T 28 54 UCEC TCGA-AX-A063 C1R SNP Missense_Mutation 12 7187873 A C 6 93 UCEC TCGA-AX-A0J1 C1R SNP Silent 12 7188502 G A 40 40 UCEC TCGA-B5-A0JZ C1R SNP Missense_Mutation 12 7244248 G T 35 52 UCEC TCGA-B5-A0K2 C1R SNP Missense_Mutation 12 7188477 C A 22 63 UCEC TCGA-B5-A11E C1R SNP Silent 12 7187965 C T 31 41 UCEC TCGA-B5-A11E C1R SNP Splice_site 12 7188604 C T 17 53 UCEC TCGA-B5-A11E C1R SNP Missense_Mutation 12 7242272 C T 25 93 UCEC TCGA-B5-A11J C1R SNP Nonsense_Mutation 12 7241271 G A 46 74 KIRC TCGA-B8-5550 C1R SNP Missense_Mutation 12 7189386 C T 26 77 HNSC TCGA-BB-7862 C1R SNP Missense_Mutation 12 7242032 C T 30 91 KIRC TCGA-BP-4158 C1R SNP Missense_Mutation 12 7188437 G T 43 68 UCEC TCGA-BS-A0TC C1R SNP Silent 12 7188421 C T 27 30 UCEC TCGA-BS-A0TC C1R SNP Missense_Mutation 12 7241295 C T 31 40 UCEC TCGA-BS-A0UF C1R SNP Silent 12 7188559 G A 37 41 UCEC TCGA-BS-A0UF C1R SNP Missense_Mutation 12 7242762 A C 1 84 UCEC TCGA-BS-A0UV C1R SNP Missense_Mutation 12 7242795 G T 33 91 UCEC TCGA-BS-A0UV C1R SNP Missense_Mutation 12 7242812 G T 33 63 BLCA TCGA-BT-A2LB C1R SNP Missense_Mutation 12 7244200 C T 21 90 KIRC TCGA-CJ-5679 C1R SNP Missense_Mutation 12 7242701 A T 8 49 HNSC TCGA-CR-7370 C1R SNP Missense_Mutation 12 7188341 C A 27 56 HNSC TCGA-CV-5441 C1R SNP Splice_Site 12 7241888 C T 18 91 UCEC TCGA-D1-A103 C1R SNP Missense_Mutation 12 7241932 A C 4 84