ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0019 LHFPL4 SNP Missense_Mutation 3 9547657 T C 62 71 LUAD LUAD-5V8LT LHFPL4 SNP Missense_Mutation 3 9594302 G T 42 93 LUAD LUAD-S01467 LHFPL4 SNP Silent 3 9547754 G A 47 85 MEL MEL-JWCI-WGS-1 LHFPL4 SNP Silent 3 9594187 G A 37 66 MEL MEL-JWCI-WGS-36 LHFPL4 SNP Missense_Mutation 3 9543951 C T 29 71 LUAD TCGA-05-4427 LHFPL4 SNP Missense_Mutation 3 9594110 C G 28 73 GBM TCGA-06-5859 LHFPL4 SNP Silent 3 9594193 G T 34 60 OV TCGA-09-1665 LHFPL4 SNP Missense_Mutation 3 9547725 A T 11 92 OV TCGA-13-0761 LHFPL4 SNP Missense_Mutation 3 9543917 A T 6 58 LUAD TCGA-17-Z046 LHFPL4 SNP Silent 3 9547772 G T 34 86 OV TCGA-23-1031 LHFPL4 SNP Silent 3 9547805 C T 23 24 LUAD TCGA-73-4668 LHFPL4 SNP Missense_Mutation 3 9594086 T C 56 87 BRCA TCGA-A2-A0T3 LHFPL4 SNP Nonsense_Mutation 3 9547779 G T 45 99 CRC TCGA-A6-2676 LHFPL4 SNP Missense_Mutation 3 9547669 G A 34 76 BRCA TCGA-A8-A093 LHFPL4 SNP Silent 3 9547748 G A 37 50 CRC TCGA-AA-A022 LHFPL4 SNP Silent 3 9547736 G A 40 53 UCEC TCGA-AX-A0J0 LHFPL4 SNP Nonsense_Mutation 3 9594190 G T 36 94 UCEC TCGA-B5-A0JR LHFPL4 SNP Splice_site 3 9547651 C A 24 85 KIRC TCGA-BP-4759 LHFPL4 SNP Missense_Mutation 3 9543917 A G 6 58 HNSC TCGA-CN-4742 LHFPL4 SNP Silent 3 9547694 C T 26 57 UCEC TCGA-D1-A103 LHFPL4 SNP Silent 3 9594358 C A 25 64 UCEC TCGA-D1-A15X LHFPL4 SNP Missense_Mutation 3 9594105 T C 51 75 BRCA TCGA-E2-A15E LHFPL4 SNP Missense_Mutation 3 9594129 C G 22 95 BLCA TCGA-GV-A3QG LHFPL4 SNP Missense_Mutation 3 9547837 C T 31 99