ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD TCGA-05-4396 FABP2 DNP Missense_Mutation 4 120240719 CG AT 31 78 OV TCGA-13-1496 FABP2 SNP Missense_Mutation 4 120240727 A T 16 48 BRCA TCGA-A8-A07R FABP2 SNP Missense_Mutation 4 120243210 G C 48 49 CRC TCGA-AA-3977 FABP2 SNP Nonsense_Mutation 4 120241935 C A 32 58 CRC TCGA-AA-A010 FABP2 SNP Silent 4 120241939 T C 59 51 CRC TCGA-AF-3913 FABP2 SNP Silent 4 120241984 C T 29 57 CRC TCGA-AG-A002 FABP2 SNP Missense_Mutation 4 120240735 C T 31 65 UCEC TCGA-AP-A054 FABP2 DEL Frame_Shift_Del 4 120241914 TGAC - 63 91 UCEC TCGA-B5-A0JY FABP2 SNP Missense_Mutation 4 120240239 A G 14 31 UCEC TCGA-B5-A11E FABP2 SNP Silent 4 120241951 C T 28 47 HNSC TCGA-CR-7388 FABP2 SNP Nonstop_Mutation 4 120240198 A T 5 71 HNSC TCGA-CV-7421 FABP2 SNP Silent 4 120243207 C T 20 56