ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-JWCI-WGS-36 CTSW SNP Missense_Mutation 11 65648962 T G 64 62 MEL MEL-Ma-Mel-19 CTSW SNP Nonsense_Mutation 11 65650798 G A 47 34 GBM TCGA-06-0876 CTSW SNP Missense_Mutation 11 65647754 G A 33 65 LUSC TCGA-18-3417 CTSW SNP Splice_Site 11 65648993 T G 57 62 LUSC TCGA-39-5031 CTSW SNP Missense_Mutation 11 65650870 C G 30 75 BRCA TCGA-A8-A09B CTSW SNP Missense_Mutation 11 65650133 G A 41 66 CRC TCGA-AA-3949 CTSW SNP Missense_Mutation 11 65649948 G T 33 60 CRC TCGA-AA-3984 CTSW SNP Splice_site 11 65648879 G A 34 56 UCEC TCGA-AP-A059 CTSW SNP Missense_Mutation 11 65650596 C T 26 64 KIRC TCGA-B0-4844 CTSW SNP Silent 11 65650835 T A 54 51 KIRC TCGA-B4-5377 CTSW SNP Missense_Mutation 11 65648930 G T 42 51 HNSC TCGA-CR-6481 CTSW SNP Silent 11 65649791 C T 29 75 HNSC TCGA-CR-6481 CTSW SNP Missense_Mutation 11 65650706 C G 29 57 BLCA TCGA-GV-A3QG CTSW SNP Missense_Mutation 11 65650570 C T 22 76