ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL ME049 CDCA3 SNP Silent 12 6959641 G A 47 57 MM MM-0460 CDCA3 SNP Missense_Mutation 12 6958277 C G 30 62 MM MM-0592 CDCA3 SNP Silent 12 6960069 C T 27 44 GBM TCGA-27-1838 CDCA3 SNP Missense_Mutation 12 6959664 T C 49 67 LUAD TCGA-35-4122 CDCA3 SNP Missense_Mutation 12 6959654 G T 48 65 BRCA TCGA-A8-A094 CDCA3 SNP Missense_Mutation 12 6958758 G A 45 50 CRC TCGA-AA-3811 CDCA3 SNP Missense_Mutation 12 6959019 G T 43 57 CRC TCGA-AA-3864 CDCA3 SNP Missense_Mutation 12 6958356 G A 38 53 CRC TCGA-AG-3881 CDCA3 SNP Missense_Mutation 12 6958846 C G 29 55 CRC TCGA-AG-A036 CDCA3 SNP Missense_Mutation 12 6958266 A G 8 56 UCEC TCGA-AP-A059 CDCA3 SNP Nonsense_Mutation 12 6958492 G A 40 68 UCEC TCGA-AP-A059 CDCA3 SNP Missense_Mutation 12 6958584 C T 27 39 HNSC TCGA-BA-4078 CDCA3 SNP Silent 12 6958258 T C 56 52 BLCA TCGA-CU-A3KJ CDCA3 SNP Missense_Mutation 12 6959647 C T 29 71 UCEC TCGA-D1-A17Q CDCA3 SNP Silent 12 6959719 T C 60 52 UCEC TCGA-DI-A0WH CDCA3 SNP Missense_Mutation 12 6958831 G C 48 64 BLCA TCGA-HQ-A2OE CDCA3 SNP Silent 12 6958994 C T 29 56