ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-076 CC2D2B SNP Silent 10 97772306 G A 35 49 LUAD LUAD-B00731 CC2D2B SNP Silent 10 97772369 C A 31 59 MEL MEL-JWCI-27 CC2D2B SNP Translation_Start_Site 10 97763954 A T 3 75 LUAD TCGA-05-4395 CC2D2B SNP Missense_Mutation 10 97769676 C A 32 68 LUAD TCGA-05-4396 CC2D2B SNP Missense_Mutation 10 97791582 G T 39 48 LUAD TCGA-05-4424 CC2D2B SNP Nonsense_Mutation 10 97776052 T A 63 76 LUAD TCGA-17-Z046 CC2D2B SNP Missense_Mutation 10 97779499 T C 57 73 OV TCGA-24-2267 CC2D2B SNP Missense_Mutation 10 97791678 A C 4 54 LUAD TCGA-55-1592 CC2D2B SNP Splice_site 10 97779094 T C 51 55 LUAD TCGA-67-6216 CC2D2B DEL Frame_Shift_Del 10 97776014 TTTC - 52 60 CRC TCGA-AG-A002 CC2D2B SNP Missense_Mutation 10 97791713 A G 2 59 UCEC TCGA-AP-A054 CC2D2B SNP Nonsense_Mutation 10 97769594 A T 5 64 UCEC TCGA-AP-A056 CC2D2B SNP Missense_Mutation 10 97769622 G A 33 52 UCEC TCGA-AP-A0LM CC2D2B SNP Missense_Mutation 10 97776058 C T 19 69 UCEC TCGA-AX-A063 CC2D2B SNP Missense_Mutation 10 97791700 C T 29 98 UCEC TCGA-AX-A0J1 CC2D2B SNP Silent 10 97776059 G A 40 49 UCEC TCGA-B5-A0JY CC2D2B SNP Missense_Mutation 10 97787034 G A 37 92 UCEC TCGA-B5-A11E CC2D2B SNP Missense_Mutation 10 97773548 C A 24 56 UCEC TCGA-B5-A11E CC2D2B SNP Nonsense_Mutation 10 97787006 C T 27 49 BLCA TCGA-CF-A1HS CC2D2B SNP Silent 10 97775978 C T 31 52 HNSC TCGA-CN-6995 CC2D2B SNP Missense_Mutation 10 97769618 A G 16 44 HNSC TCGA-CV-7418 CC2D2B SNP Missense_Mutation 10 97779477 C G 17 66 KIRC TCGA-CZ-4861 CC2D2B SNP Missense_Mutation 10 97791691 G T 48 98 UCEC TCGA-D1-A160 CC2D2B SNP Missense_Mutation 10 97775979 G A 39 68 UCEC TCGA-D1-A16Y CC2D2B SNP Nonsense_Mutation 10 97772445 C T 25 66 BLCA TCGA-DK-A2I4 CC2D2B SNP Missense_Mutation 10 97772423 C G 29 67