ttype patient gene classification type chr pos ref_allele newbase context65 cons46 PRAD PR-1043 KLF9 SNP Missense_Mutation 9 73002756 C T 23 87 GBM TCGA-28-5214 KLF9 SNP Missense_Mutation 9 73002796 G A 38 70 LUSC TCGA-66-2759 KLF9 SNP Missense_Mutation 9 73028180 C G 31 63 UCEC TCGA-AP-A059 KLF9 SNP Missense_Mutation 9 73027796 C T 28 77 UCEC TCGA-AX-A06H KLF9 SNP Missense_Mutation 9 73028002 A G 8 66 KIRC TCGA-B0-5697 KLF9 SNP Silent 9 73027803 A G 12 65 KIRC TCGA-BP-4159 KLF9 SNP Silent 9 73027905 G A 43 64 BLCA TCGA-C4-A0EZ KLF9 SNP Silent 9 73002701 G A 40 58 KIRC TCGA-CJ-4634 KLF9 SNP Missense_Mutation 9 73028059 C A 31 92 KIRC TCGA-CJ-4637 KLF9 SNP Nonsense_Mutation 9 73027946 C A 30 91 HNSC TCGA-CQ-6224 KLF9 SNP Nonsense_Mutation 9 73002724 G A 38 62 KIRC TCGA-CZ-4866 KLF9 SNP Silent 9 73027890 T C 54 56 UCEC TCGA-D1-A16X KLF9 SNP Missense_Mutation 9 73002723 C T 31 74