ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62672 IFT27 SNP Missense 22 37158997 G A 42 87 MM MM-0457 IFT27 SNP Nonsense_Mutation 22 37160061 A C 13 82 LUSC TCGA-63-5128 IFT27 SNP Missense_Mutation 22 37163876 G C 46 57 UCEC TCGA-AP-A051 IFT27 SNP Silent 22 37158951 G T 39 34 UCEC TCGA-AP-A059 IFT27 SNP Silent 22 37160027 G T 35 52 UCEC TCGA-AX-A0J0 IFT27 SNP Silent 22 37154436 G A 37 38 UCEC TCGA-B5-A0K6 IFT27 SNP Missense_Mutation 22 37154365 G A 42 62 UCEC TCGA-D1-A174 IFT27 SNP Missense_Mutation 22 37163864 C T 27 67