ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-118 DPCD SNP Missense_Mutation 10 103360507 G A 40 94 LUAD TCGA-17-Z031 DPCD SNP Silent 10 103348126 G T 41 71 LUSC TCGA-18-3409 DPCD SNP Silent 10 103360569 C T 24 57 LUSC TCGA-21-1076 DPCD SNP Missense_Mutation 10 103354462 G C 45 80 CRC TCGA-AA-A01R DPCD SNP Missense_Mutation 10 103368671 G A 38 75 UCEC TCGA-AP-A051 DPCD SNP Silent 10 103354446 C T 19 52 UCEC TCGA-AP-A059 DPCD SNP Missense_Mutation 10 103360506 C T 27 63 UCEC TCGA-AX-A05Y DPCD SNP Missense_Mutation 10 103361062 C T 27 72 UCEC TCGA-B5-A11E DPCD SNP Missense_Mutation 10 103348139 A G 10 79 HNSC TCGA-CR-6484 DPCD SNP Missense_Mutation 10 103360965 C G 32 55 HNSC TCGA-CV-5432 DPCD SNP Missense_Mutation 10 103360557 G C 33 94 BRCA TCGA-D8-A1Y3 DPCD SNP Missense_Mutation 10 103360972 C T 27 65