ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CW108 CLCN2 SNP Missense_Mutation 3 184076875 C G 24 54 ESO ESO-682 CLCN2 SNP Silent 3 184075020 C T 26 50 HNSC HN_62814 CLCN2 SNP Missense 3 184076909 C T 23 93 LUAD LUAD-E00934 CLCN2 SNP Splice_Site 3 184074969 C A 18 97 MEL ME044 CLCN2 SNP Splice_site 3 184069801 C T 24 82 MEL MEL-13473 CLCN2 SNP Silent 3 184075029 G A 43 47 MEL MEL-JWCI-WGS-1 CLCN2 SNP Silent 3 184070897 C T 22 52 MEL MEL-JWCI-WGS-12 CLCN2 SNP Silent 3 184075873 G A 41 65 MEL MEL-JWCI-WGS-32 CLCN2 SNP Missense_Mutation 3 184070896 C T 30 67 MEL MEL-Ma-Mel-119 CLCN2 SNP Silent 3 184072746 G A 36 62 MM MM-0538 CLCN2 SNP Silent 3 184071571 C T 25 53 GBM TCGA-06-0219 CLCN2 SNP Missense_Mutation 3 184071135 C T 27 86 OV TCGA-13-0919 CLCN2 SNP Missense_Mutation 3 184070929 T A 59 54 LUSC TCGA-18-3409 CLCN2 SNP Silent 3 184071921 G A 35 59 LUSC TCGA-18-3409 CLCN2 SNP Missense_Mutation 3 184075218 C T 23 85 LUSC TCGA-18-4083 CLCN2 SNP Missense_Mutation 3 184075171 C T 26 84 LUSC TCGA-34-2596 CLCN2 SNP Missense_Mutation 3 184075201 T A 59 76 LUSC TCGA-34-5239 CLCN2 SNP Silent 3 184074816 C G 30 54 LUSC TCGA-43-5668 CLCN2 SNP Missense_Mutation 3 184076563 C A 18 66 LUAD TCGA-44-3918 CLCN2 SNP Missense_Mutation 3 184076898 C A 30 93 LUSC TCGA-85-6561 CLCN2 SNP Silent 3 184075157 C A 22 40 CRC TCGA-AA-3976 CLCN2 SNP Missense_Mutation 3 184076771 C T 31 44 CRC TCGA-AA-3986 CLCN2 SNP Missense_Mutation 3 184064546 T C 62 89 CRC TCGA-AA-A00N CLCN2 SNP Silent 3 184075424 G A 37 47 CRC TCGA-AA-A00Z CLCN2 SNP Missense_Mutation 3 184064426 T C 55 68 AML TCGA-AB-2828 CLCN2 SNP Missense_Mutation 3 184072054 A C 6 90 CRC TCGA-AG-A02N CLCN2 SNP Missense_Mutation 3 184075230 C T 23 85 UCEC TCGA-AP-A051 CLCN2 SNP Missense_Mutation 3 184075622 C T 28 97 UCEC TCGA-AP-A059 CLCN2 SNP Missense_Mutation 3 184071135 C T 27 86 UCEC TCGA-AP-A059 CLCN2 SNP Missense_Mutation 3 184071983 C T 27 99 UCEC TCGA-AX-A0J1 CLCN2 SNP Missense_Mutation 3 184074797 G A 37 70 KIRC TCGA-B0-5109 CLCN2 SNP Missense_Mutation 3 184064449 C T 19 60 UCEC TCGA-B5-A0JY CLCN2 SNP Missense_Mutation 3 184076907 A G 14 85 UCEC TCGA-B5-A11Y CLCN2 SNP Missense_Mutation 3 184064584 C T 23 84 BRCA TCGA-B6-A0IO CLCN2 SNP Missense_Mutation 3 184070098 C T 31 60 HNSC TCGA-BA-5555 CLCN2 SNP Splice_site 3 184069802 T G 56 88 UCEC TCGA-BS-A0TA CLCN2 SNP Missense_Mutation 3 184072070 T C 59 90 UCEC TCGA-BS-A0UV CLCN2 SNP Silent 3 184072044 G A 37 63 KIRC TCGA-CJ-4895 CLCN2 DEL Frame_Shift_Del 3 184064478 CT - 24 62 HNSC TCGA-CN-5359 CLCN2 SNP Missense_Mutation 3 184071144 C T 28 100 HNSC TCGA-CN-6018 CLCN2 SNP Silent 3 184074822 C T 29 68 HNSC TCGA-CV-5441 CLCN2 SNP Missense_Mutation 3 184076565 C T 24 71 HNSC TCGA-CV-7099 CLCN2 DEL Frame_Shift_Del 3 184079208 GGTCTGCTCGTACT - 43 54 KIRC TCGA-CW-5580 CLCN2 SNP Missense_Mutation 3 184070571 A G 11 79 KIRC TCGA-CW-6093 CLCN2 SNP Silent 3 184079226 C G 27 54 UCEC TCGA-D1-A167 CLCN2 SNP Missense_Mutation 3 184072081 G A 38 99 UCEC TCGA-D1-A174 CLCN2 DEL Frame_Shift_Del 3 184070829 CT - 20 63 HNSC TCGA-D6-6516 CLCN2 SNP Missense_Mutation 3 184064422 G C 35 67 HNSC TCGA-D6-6516 CLCN2 SNP Silent 3 184071990 C T 21 83 BRCA TCGA-EW-A1IZ CLCN2 SNP Missense_Mutation 3 184069902 G T 33 63 BRCA TCGA-EW-A1IZ CLCN2 SNP Splice_Site 3 184072690 A G 6 91 CARC Carc-H56 CLCN2 SNP Missense_Mutation 3 184079234 G C 42 60