ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-B00731 FEN1 SNP Missense_Mutation 11 61563408 G T 37 86 MEL MEL-JWCI-WGS-1 FEN1 DNP Silent 11 61562848 CC TT 26 51 MM MM-0282 FEN1 SNP Missense_Mutation 11 61563474 A G 7 88 MM MM-0319 FEN1 SNP Synonymous 11 61563364 C T 23 2 LUAD TCGA-05-4396 FEN1 SNP Silent 11 61563076 C A 23 10 OV TCGA-13-0755 FEN1 SNP Missense_Mutation 11 61563786 A T 11 90 BRCA TCGA-A8-A06X FEN1 SNP Missense_Mutation 11 61563621 T A 56 91 CRC TCGA-AA-A00A FEN1 SNP Missense_Mutation 11 61563459 T C 55 87 CRC TCGA-AA-A010 FEN1 SNP Missense_Mutation 11 61562893 G T 33 72 CRC TCGA-AA-A022 FEN1 SNP Missense_Mutation 11 61563566 C G 27 66 CRC TCGA-AG-A002 FEN1 SNP Missense_Mutation 11 61563819 G A 36 56 KIRC TCGA-B0-5694 FEN1 INS Frame_Shift_Ins 11 61563635 - AC 57 68 UCEC TCGA-B5-A11E FEN1 SNP Nonsense_Mutation 11 61563791 C T 27 64 UCEC TCGA-B5-A11H FEN1 SNP Missense_Mutation 11 61563474 A C 7 88 UCEC TCGA-BS-A0U8 FEN1 SNP Silent 11 61563826 C T 26 79 HNSC TCGA-CR-7399 FEN1 SNP Missense_Mutation 11 61563897 G T 38 87