ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62857_2 KLF14 SNP Missense 7 130418509 T A 50 49 MEL ME045 KLF14 SNP Missense_Mutation 7 130417902 G A 44 59 MEL MEL-Ma-Mel-65 KLF14 SNP Missense_Mutation 7 130418244 T A 49 84 LUAD TCGA-05-4382 KLF14 SNP Missense_Mutation 7 130418206 G T 47 91 CRC TCGA-AA-3518 KLF14 SNP Missense_Mutation 7 130418034 C T 27 78 CRC TCGA-AA-A01R KLF14 SNP Silent 7 130418117 C T 27 47 CRC TCGA-AG-3586 KLF14 SNP Missense_Mutation 7 130418037 C A 27 65 CRC TCGA-AG-A02N KLF14 INS Frame_Shift_Ins 7 130418544 - C 62 50 UCEC TCGA-AP-A0LM KLF14 SNP Silent 7 130418231 C T 27 52 UCEC TCGA-B5-A11E KLF14 SNP Missense_Mutation 7 130417908 C A 28 65 HNSC TCGA-CN-5360 KLF14 SNP Missense_Mutation 7 130418350 G C 35 59 HNSC TCGA-CV-6962 KLF14 SNP Missense_Mutation 7 130418557 C T 30 64 HNSC TCGA-CV-7406 KLF14 SNP Missense_Mutation 7 130417929 G A 41 59 UCEC TCGA-D1-A103 KLF14 SNP Missense_Mutation 7 130417939 C T 27 54 UCEC TCGA-D1-A17Q KLF14 SNP Silent 7 130418270 G A 42 67