ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0019 FICD SNP Missense_Mutation 12 108913117 C G 29 89 HNSC HN_62686 FICD SNP Missense 12 108912654 A C 11 94 HNSC HN_62854 FICD SNP Missense 12 108912218 G C 41 96 LUAD LUAD-B02077 FICD SNP Missense_Mutation 12 108910864 G T 42 59 LUAD TCGA-05-5425 FICD SNP Missense_Mutation 12 108912393 A T 8 77 LUSC TCGA-66-2794 FICD SNP Splice_site 12 108910749 G C 33 81 UCEC TCGA-A5-A0VQ FICD SNP Nonsense_Mutation 12 108912863 C T 25 100 CRC TCGA-AA-3514 FICD SNP Missense_Mutation 12 108912998 C G 32 67 CRC TCGA-AA-3672 FICD SNP Silent 12 108912203 C T 24 59 CRC TCGA-AA-3864 FICD SNP Silent 12 108910974 C T 25 53 CRC TCGA-AA-A00K FICD SNP Missense_Mutation 12 108912294 T A 59 69 CRC TCGA-AA-A010 FICD SNP Silent 12 108913102 C T 27 50 CRC TCGA-AA-A01D FICD SNP Missense_Mutation 12 108913238 C T 30 75 CRC TCGA-AG-A00Y FICD SNP Missense_Mutation 12 108913095 A T 2 94 CRC TCGA-AG-A00Y FICD SNP Missense_Mutation 12 108913103 G A 37 100 UCEC TCGA-AP-A056 FICD SNP Silent 12 108912415 C T 27 53 UCEC TCGA-B5-A11E FICD SNP Missense_Mutation 12 108912396 A C 11 69 BRCA TCGA-B6-A0IP FICD SNP Silent 12 108913081 G A 48 43 UCEC TCGA-BS-A0TJ FICD SNP Missense_Mutation 12 108912635 C T 26 70 UCEC TCGA-BS-A0UJ FICD SNP Missense_Mutation 12 108912197 G A 34 96 UCEC TCGA-BS-A0UJ FICD SNP Missense_Mutation 12 108912305 A C 6 89 UCEC TCGA-BS-A0UV FICD SNP Silent 12 108912469 C T 31 55 UCEC TCGA-D1-A163 FICD SNP Silent 12 108910879 C T 28 78 BLCA TCGA-FD-A3N5 FICD SNP Silent 12 108912880 A G 14 9