ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_00378 CKLF SNP Synonymous 16 66592176 C T 23 38 LUAD TCGA-05-4396 CKLF SNP Silent 16 66592176 C A 23 38 LUSC TCGA-18-3410 CKLF SNP Missense_Mutation 16 66592182 C G 32 55 UCEC TCGA-AP-A056 CKLF SNP Missense_Mutation 16 66597100 A G 2 46 UCEC TCGA-AP-A059 CKLF SNP Missense_Mutation 16 66597060 G A 46 63 UCEC TCGA-AP-A0LM CKLF SNP Missense_Mutation 16 66592135 G T 34 75 KIRC TCGA-B8-4622 CKLF SNP Silent 16 66599818 T C 58 48 HNSC TCGA-BB-7871 CKLF SNP Missense_Mutation 16 66597056 T C 62 60 BLCA TCGA-BT-A2LD CKLF SNP Silent 16 66592158 C T 29 75 HNSC TCGA-CV-7095 CKLF SNP Missense_Mutation 16 66597116 G A 41 74 UCEC TCGA-D1-A16X CKLF SNP Missense_Mutation 16 66592130 C T 25 64 UCEC TCGA-D1-A16Y CKLF SNP Silent 16 66592128 C T 31 37 BRCA TCGA-D8-A147 CKLF SNP Missense_Mutation 16 66592170 A T 3 61