ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0004 CCDC77 SNP Missense 12 551076 G C 33 84 ESO ESO-021 CCDC77 SNP Missense_Mutation 12 550989 T C 58 90 LUAD LUAD-U6SJ7 CCDC77 SNP Splice_Site 12 521145 G T 44 98 MEL MEL-JWCI-WGS-36 CCDC77 SNP Missense_Mutation 12 550955 C T 23 68 LUAD TCGA-05-4396 CCDC77 SNP Silent 12 538004 C A 24 51 LUAD TCGA-05-4396 CCDC77 SNP Silent 12 542375 C A 21 48 LUAD TCGA-05-4396 CCDC77 SNP Silent 12 549867 C A 23 59 OV TCGA-09-2050 CCDC77 SNP Silent 12 549794 T C 49 49 LUSC TCGA-39-5031 CCDC77 SNP Missense_Mutation 12 521043 G C 41 99 LUSC TCGA-39-5035 CCDC77 SNP Missense_Mutation 12 549899 G C 33 55 CRC TCGA-AA-3715 CCDC77 SNP Silent 12 541060 G A 37 47 CRC TCGA-AA-3877 CCDC77 SNP Silent 12 542408 C T 31 57 CRC TCGA-AA-3966 CCDC77 SNP Missense_Mutation 12 550055 C T 19 87 CRC TCGA-AG-A002 CCDC77 SNP Missense_Mutation 12 547544 T G 64 75 CRC TCGA-AG-A002 CCDC77 SNP Missense_Mutation 12 551073 T G 56 90 UCEC TCGA-AP-A059 CCDC77 SNP Missense_Mutation 12 549873 C T 31 66 UCEC TCGA-AX-A063 CCDC77 SNP Missense_Mutation 12 551007 G A 39 64 KIRC TCGA-B0-4823 CCDC77 DEL Splice_Site 12 518533 G - 35 77 UCEC TCGA-BS-A0UJ CCDC77 SNP Missense_Mutation 12 549859 A G 9 92 HNSC TCGA-CN-4726 CCDC77 SNP Missense_Mutation 12 539877 G C 33 58 HNSC TCGA-CN-5369 CCDC77 SNP Missense_Mutation 12 551063 G C 41 98 BLCA TCGA-DK-A1A3 CCDC77 SNP Missense_Mutation 12 538021 C T 24 98