ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CW179 FIGNL2 SNP Silent 12 52215307 G T 39 51 DLBCL DLBCL-MAYO_DLBCL_234 FIGNL2 SNP Silent 12 52216054 G A 40 61 HNSC HN_62921 FIGNL2 SNP Missense 12 52216085 C T 18 60 MEL MEL-JWCI-WGS-18 FIGNL2 SNP Missense_Mutation 12 52215954 C A 23 59 MM MM-0633 FIGNL2 SNP Missense_Mutation 12 52215954 C T 23 59 LUSC TCGA-18-3419 FIGNL2 SNP Silent 12 52216039 G A 43 50 LUAD TCGA-64-5781 FIGNL2 SNP Missense_Mutation 12 52215878 G T 43 67 CRC TCGA-AA-3864 FIGNL2 SNP Silent 12 52215925 G A 38 39 CRC TCGA-AA-3866 FIGNL2 SNP Missense_Mutation 12 52215893 G A 39 74 CRC TCGA-AA-3947 FIGNL2 SNP Silent 12 52216051 G A 40 50 UCEC TCGA-AP-A059 FIGNL2 SNP Missense_Mutation 12 52215992 C T 22 82 UCEC TCGA-AP-A0LM FIGNL2 SNP Missense_Mutation 12 52215956 C T 26 70 KIRC TCGA-CJ-4639 FIGNL2 SNP Splice_site 12 52216199 T G 56 75 HNSC TCGA-CN-5356 FIGNL2 SNP Missense_Mutation 12 52215791 G C 42 72 UCEC TCGA-D1-A161 FIGNL2 SNP Silent 12 52216120 C T 19 49