ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CW175 FHL2 SNP Silent 2 106002833 G A 37 48 LUAD LUAD-B00915 FHL2 SNP Splice_site 2 105990189 T A 58 90 MEL MEL-JWCI-WGS-38 FHL2 SNP Silent 2 105990029 C T 32 74 MEL MEL-JWCI-WGS-7 FHL2 SNP Silent 2 105990149 G A 41 70 MM MM-0408 FHL2 SNP Synonymous 2 105977743 G T 33 65 LUSC TCGA-22-5474 FHL2 SNP Missense_Mutation 2 105990063 T C 60 77 OV TCGA-24-1464 FHL2 SNP Silent 2 105990124 G A 36 73 CRC TCGA-AA-A010 FHL2 SNP Missense_Mutation 2 105979817 C A 29 87 CRC TCGA-AG-A002 FHL2 SNP Missense_Mutation 2 105977855 C T 23 88 BRCA TCGA-AR-A0U4 FHL2 SNP Missense_Mutation 2 105990062 G T 40 51 UCEC TCGA-AX-A0J1 FHL2 SNP Missense_Mutation 2 105979835 G A 38 68 HNSC TCGA-CV-5430 FHL2 INS Frame_Shift_Ins 2 105977793 - G 3 92 KIRC TCGA-CZ-5468 FHL2 SNP Missense_Mutation 2 105977880 T C 59 72 UCEC TCGA-D1-A103 FHL2 SNP Missense_Mutation 2 106002940 C T 31 89 BRCA TCGA-D8-A1JP FHL2 SNP Missense_Mutation 2 105979846 A T 7 92