ttype patient gene classification type chr pos ref_allele newbase context65 cons46 PRAD PR-02-1736 KCTD21 SNP Silent 11 77885549 G A 36 71 LUSC TCGA-39-5019 KCTD21 SNP Missense_Mutation 11 77885071 T C 59 84 LUSC TCGA-56-6545 KCTD21 SNP Nonsense_Mutation 11 77885471 G A 47 75 CRC TCGA-AA-3667 KCTD21 SNP Missense_Mutation 11 77884970 C G 18 69 CRC TCGA-AA-A00N KCTD21 SNP Silent 11 77885523 G A 36 72 CRC TCGA-AG-A002 KCTD21 SNP Nonsense_Mutation 11 77884838 G A 37 82 CRC TCGA-AG-A002 KCTD21 SNP Silent 11 77885445 G A 40 49 UCEC TCGA-AP-A056 KCTD21 SNP Silent 11 77885091 A G 12 47 UCEC TCGA-AX-A05S KCTD21 SNP Missense_Mutation 11 77885236 G A 40 55 UCEC TCGA-AX-A05Z KCTD21 SNP Silent 11 77885040 G A 36 58 KIRC TCGA-B0-4693 KCTD21 SNP Silent 11 77885169 G A 45 90 UCEC TCGA-B5-A11E KCTD21 SNP Silent 11 77884839 A G 9 50 UCEC TCGA-B5-A11E KCTD21 SNP Missense_Mutation 11 77885195 G A 35 72 BRCA TCGA-B6-A0I2 KCTD21 SNP Missense_Mutation 11 77884970 C A 18 69 BRCA TCGA-BH-A0BZ KCTD21 SNP Nonsense_Mutation 11 77885303 C A 30 81 BRCA TCGA-C8-A137 KCTD21 SNP Missense_Mutation 11 77885216 C T 31 71 HNSC TCGA-CN-4723 KCTD21 SNP Missense_Mutation 11 77884871 G A 48 84