ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0027 FGFR1OP2 SNP Missense_Mutation 12 27117660 G T 33 58 MEL MEL-UKRV-Mel-24 FGFR1OP2 SNP Missense_Mutation 12 27116318 T C 57 77 LUAD TCGA-05-4396 FGFR1OP2 SNP Silent 12 27110593 C A 23 57 CRC TCGA-AA-3811 FGFR1OP2 SNP Silent 12 27110625 C T 25 85 CRC TCGA-AA-A00N FGFR1OP2 SNP Missense_Mutation 12 27113451 G T 45 64 CRC TCGA-AA-A03F FGFR1OP2 SNP Silent 12 27110640 G A 39 46 CRC TCGA-AG-A002 FGFR1OP2 SNP Missense_Mutation 12 27113500 G A 37 59 UCEC TCGA-AP-A059 FGFR1OP2 SNP Nonsense_Mutation 12 27109491 C T 29 69 UCEC TCGA-AP-A0LM FGFR1OP2 SNP Nonsense_Mutation 12 27109584 G T 33 98 UCEC TCGA-B5-A11E FGFR1OP2 SNP Nonsense_Mutation 12 27109485 G T 33 99 UCEC TCGA-B5-A11N FGFR1OP2 SNP Missense_Mutation 12 27117626 C T 25 62 UCEC TCGA-BS-A0UV FGFR1OP2 SNP Splice_Site 12 27110533 G T 33 99 UCEC TCGA-D1-A103 FGFR1OP2 SNP Missense_Mutation 12 27113463 C T 31 65 UCEC TCGA-D1-A16Y FGFR1OP2 SNP Missense_Mutation 12 27116348 A G 5 58 HNSC TCGA-DQ-5625 FGFR1OP2 SNP Splice_site 12 27113571 A G 4 55