ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-Ls3808 CTSC SNP Missense_Mutation 11 88068135 C G 29 67 LUAD LUAD_E00565 CTSC SNP Missense_Mutation 11 88042353 C G 21 76 MEL ME012 CTSC SNP Missense_Mutation 11 88027401 G A 47 89 MEL MEL-JWCI-14 CTSC SNP Silent 11 88027344 G A 33 72 MEL MEL-JWCI-WGS-12 CTSC SNP Missense_Mutation 11 88027560 C T 32 56 MEL MEL-JWCI-WGS-12 CTSC SNP Missense_Mutation 11 88029381 C T 32 100 MEL MEL-JWCI-WGS-34 CTSC SNP Splice_site 11 88061365 C T 24 66 MEL MEL-JWCI-WGS-6 CTSC SNP Silent 11 88068114 G A 35 57 MEL MEL-Ma-Mel-48 CTSC SNP Missense_Mutation 11 88027434 C T 29 52 NB NB-0997 CTSC SNP Silent 11 88070790 G T 39 45 LUAD TCGA-05-4396 CTSC SNP Nonsense_Mutation 11 88027536 C A 29 73 LUAD TCGA-05-4396 CTSC SNP Silent 11 88045627 G T 39 35 OV TCGA-23-2081 CTSC SNP Missense_Mutation 11 88070831 C A 21 18 OV TCGA-30-1891 CTSC SNP Nonsense_Mutation 11 88042468 G T 48 61 LUAD TCGA-35-3621 CTSC SNP Missense_Mutation 11 88045565 G C 33 45 LUSC TCGA-43-2578 CTSC SNP Missense_Mutation 11 88033701 G C 47 99 LUAD TCGA-44-2668 CTSC SNP Silent 11 88027474 C T 21 64 LUSC TCGA-66-2763 CTSC SNP Silent 11 88029410 T G 51 53 CRC TCGA-AA-3672 CTSC SNP Missense_Mutation 11 88045626 C T 23 95 CRC TCGA-AA-3811 CTSC SNP Missense_Mutation 11 88068176 G T 47 61 CRC TCGA-AA-3877 CTSC SNP Silent 11 88068132 A G 8 47 CRC TCGA-AA-3984 CTSC SNP Nonsense_Mutation 11 88033707 G A 37 59 CRC TCGA-AA-A00N CTSC SNP Nonsense_Mutation 11 88045716 C A 32 46 CRC TCGA-AG-A002 CTSC SNP Missense_Mutation 11 88045581 C T 28 53 UCEC TCGA-AP-A056 CTSC SNP Missense_Mutation 11 88027550 C T 19 71 UCEC TCGA-AX-A05Z CTSC SNP Nonsense_Mutation 11 88033707 G A 37 59 UCEC TCGA-AX-A0J1 CTSC SNP Silent 11 88033768 C T 25 50 CRC TCGA-AY-4071 CTSC SNP Missense_Mutation 11 88033724 T C 52 90 UCEC TCGA-B5-A0JY CTSC SNP Missense_Mutation 11 88042343 C T 31 47 UCEC TCGA-BS-A0UF CTSC SNP Missense_Mutation 11 88027375 G T 45 68 HNSC TCGA-CR-7388 CTSC SNP Missense_Mutation 11 88027277 C A 26 100