ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CLL_064 HVCN1 SNP Missense_Mutation 12 111089127 C A 18 54 DLBCL DLBCL-LS4592 HVCN1 SNP Missense_Mutation 12 111089051 C T 23 87 ESO ESO-0129 HVCN1 SNP Splice_site 12 111093141 G A 45 44 LUAD LUAD-F00368 HVCN1 SNP Missense_Mutation 12 111089042 C T 23 100 MEL MEL-Ma-Mel-119 HVCN1 SNP Silent 12 111088078 G A 45 50 MM MM-0473 HVCN1 SNP Missense_Mutation 12 111099142 A T 8 79 PRAD P09-649 HVCN1 SNP Silent 12 111099083 G A 38 45 LUAD TCGA-05-4389 HVCN1 SNP Silent 12 111099152 G A 36 56 LUAD TCGA-05-4398 HVCN1 SNP Silent 12 111088015 C T 21 53 LUAD TCGA-17-Z022 HVCN1 SNP Missense_Mutation 12 111088062 G T 40 84 LUAD TCGA-17-Z031 HVCN1 SNP Missense_Mutation 12 111099189 G A 40 67 GBM TCGA-28-5219 HVCN1 SNP Silent 12 111099035 G A 39 36 GBM TCGA-32-2491 HVCN1 SNP Silent 12 111099056 G A 40 32 GBM TCGA-32-4211 HVCN1 SNP Missense_Mutation 12 111089040 C A 18 87 LUSC TCGA-33-4566 HVCN1 SNP Silent 12 111099059 A T 7 29 LUAD TCGA-55-1592 HVCN1 SNP Missense_Mutation 12 111099066 G A 46 47 BRCA TCGA-A2-A0ER HVCN1 SNP Missense_Mutation 12 111089194 T G 52 54 CRC TCGA-AA-3555 HVCN1 SNP Silent 12 111089029 G T 45 63 CRC TCGA-AA-3854 HVCN1 SNP Missense_Mutation 12 111088020 G T 48 71 CRC TCGA-AA-3984 HVCN1 SNP Missense_Mutation 12 111089070 C A 22 87 CRC TCGA-AA-A01R HVCN1 SNP Silent 12 111089113 G A 37 39 CRC TCGA-AG-A02N HVCN1 SNP Missense_Mutation 12 111093101 G A 34 80 UCEC TCGA-AX-A0J0 HVCN1 SNP Nonsense_Mutation 12 111087247 G A 38 52 UCEC TCGA-AX-A0J1 HVCN1 SNP Missense_Mutation 12 111088062 G A 40 84 KIRC TCGA-B0-5695 HVCN1 SNP Missense_Mutation 12 111089162 T C 59 92 UCEC TCGA-B5-A11E HVCN1 SNP Splice_Site 12 111093144 C A 24 95 UCEC TCGA-B5-A11H HVCN1 SNP Missense_Mutation 12 111088053 G A 40 64 UCEC TCGA-BK-A0C9 HVCN1 SNP Silent 12 111089095 G A 41 51 KIRC TCGA-BP-4771 HVCN1 SNP Splice_Site 12 111099084 C T 26 54 UCEC TCGA-BS-A0UV HVCN1 SNP Missense_Mutation 12 111099203 G T 33 68 HNSC TCGA-CN-4723 HVCN1 SNP Missense_Mutation 12 111099112 C T 30 58 HNSC TCGA-CV-7245 HVCN1 SNP Missense_Mutation 12 111089187 C G 17 78 KIRC TCGA-CZ-4853 HVCN1 INS Frame_Shift_Ins 12 111089051 - T 23 87 KIRC TCGA-CZ-4853 HVCN1 SNP Silent 12 111089052 G T 39 77 HNSC TCGA-HD-7917 HVCN1 SNP Nonsense_Mutation 12 111099133 C A 29 84