ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-114 FEM1C SNP Missense_Mutation 5 114860388 C A 30 100 HNSC HN_62421 FEM1C SNP Missense 5 114860250 G C 33 66 LUAD LUAD-B00915 FEM1C SNP Missense_Mutation 5 114861281 C G 30 87 LUAD LUAD-YINHD FEM1C SNP Missense_Mutation 5 114860931 C A 24 63 MEL MEL-JWCI-WGS-11 FEM1C SNP Missense_Mutation 5 114860738 G A 35 100 LUAD TCGA-17-Z026 FEM1C SNP Silent 5 114860290 G A 45 78 LUSC TCGA-18-3410 FEM1C SNP Missense_Mutation 5 114879045 G C 42 100 OV TCGA-24-1427 FEM1C SNP Missense_Mutation 5 114878877 T C 51 71 LUAD TCGA-67-3771 FEM1C SNP Silent 5 114879140 C A 26 47 CRC TCGA-AG-3898 FEM1C SNP Silent 5 114860764 C T 21 77 UCEC TCGA-AP-A051 FEM1C SNP Missense_Mutation 5 114861119 G T 34 100 UCEC TCGA-AP-A059 FEM1C SNP Missense_Mutation 5 114860309 C T 17 100 UCEC TCGA-AP-A0LM FEM1C SNP Silent 5 114860293 G A 40 52 UCEC TCGA-AP-A0LM FEM1C SNP Missense_Mutation 5 114878712 C A 30 100 UCEC TCGA-B5-A11O FEM1C SNP Missense_Mutation 5 114860661 C T 24 100 KIRC TCGA-BP-4774 FEM1C SNP Missense_Mutation 5 114860558 T C 58 79 KIRC TCGA-BP-5185 FEM1C SNP Missense_Mutation 5 114878826 G A 34 100 UCEC TCGA-BS-A0UF FEM1C SNP Silent 5 114860835 T G 53 61 UCEC TCGA-BS-A0UF FEM1C SNP Nonsense_Mutation 5 114860958 C A 30 100 UCEC TCGA-BS-A0UV FEM1C SNP Missense_Mutation 5 114861238 C A 32 70 KIRC TCGA-CZ-5470 FEM1C SNP Missense_Mutation 5 114860153 T C 50 90 UCEC TCGA-D1-A16F FEM1C SNP Missense_Mutation 5 114860915 G T 35 100 UCEC TCGA-D1-A16X FEM1C SNP Missense_Mutation 5 114860292 C T 19 82 UCEC TCGA-DI-A0WH FEM1C SNP Silent 5 114879071 A G 8 47 BLCA TCGA-DK-A1AC FEM1C SNP Missense_Mutation 5 114878661 C G 32 100 BLCA TCGA-DK-A1AC FEM1C SNP Silent 5 114879143 G A 41 60 CARC Carc-BWH1 FEM1C SNP Silent 5 114860929 A T 10 49 CARC Carc-H56 FEM1C SNP Missense_Mutation 5 114878950 T A 51 92