ttype patient gene classification type chr pos ref_allele newbase context65 cons46 OV TCGA-04-1338 ZCCHC17 SNP Missense_Mutation 1 31811817 G C 33 72 GBM TCGA-14-0790 ZCCHC17 INS Splice_Site 1 31810124 - A 57 81 LUAD TCGA-17-Z056 ZCCHC17 SNP Missense_Mutation 1 31810024 C G 32 68 BRCA TCGA-A2-A0YK ZCCHC17 SNP Nonsense_Mutation 1 31811816 A T 15 81 UCEC TCGA-A5-A0GI ZCCHC17 SNP Missense_Mutation 1 31810057 G C 44 90 CRC TCGA-AA-3518 ZCCHC17 SNP Missense_Mutation 1 31810107 G T 34 64 CRC TCGA-AA-A010 ZCCHC17 SNP Missense_Mutation 1 31782975 A C 1 49 KIRC TCGA-AK-3430 ZCCHC17 DEL Frame_Shift_Del 1 31836865 AATTTTCTTTTCAGGAGAAG - 1 49 UCEC TCGA-AP-A059 ZCCHC17 SNP Silent 1 31837019 C T 17 51 UCEC TCGA-AX-A05Z ZCCHC17 SNP Missense_Mutation 1 31810034 G A 37 55 KIRC TCGA-B0-5120 ZCCHC17 SNP Missense_Mutation 1 31782970 A G 8 57 KIRC TCGA-B8-5550 ZCCHC17 SNP Missense_Mutation 1 31836934 A C 10 69 UCEC TCGA-BS-A0UV ZCCHC17 SNP Missense_Mutation 1 31810034 G A 37 55 HNSC TCGA-CV-7255 ZCCHC17 SNP Missense_Mutation 1 31837035 G C 41 55