ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-JWCI-WGS-1 FAIM2 SNP Missense_Mutation 12 50284500 T C 51 78 MEL MEL-JWCI-WGS-1 FAIM2 SNP Missense_Mutation 12 50295006 C T 30 76 MM MM-0449 FAIM2 SNP Missense_Mutation 12 50283302 C A 17 81 MM MM-0641 FAIM2 SNP Silent 12 50283309 C T 23 37 LUAD TCGA-05-4396 FAIM2 SNP Missense_Mutation 12 50290823 C A 21 66 LUAD TCGA-17-Z030 FAIM2 SNP Missense_Mutation 12 50281194 G T 46 53 LUAD TCGA-17-Z031 FAIM2 SNP Silent 12 50284484 C A 29 58 LUAD TCGA-17-Z049 FAIM2 SNP Missense_Mutation 12 50294975 C A 22 76 OV TCGA-23-1021 FAIM2 SNP Missense_Mutation 12 50282968 G A 42 70 LUAD TCGA-38-4632 FAIM2 SNP Missense_Mutation 12 50282944 G A 45 71 LUAD TCGA-50-5946 FAIM2 SNP Silent 12 50291869 G A 46 63 LUAD TCGA-50-5946 FAIM2 SNP Splice_site 12 50291871 T A 55 51 LUSC TCGA-60-2708 FAIM2 SNP Missense_Mutation 12 50264382 G T 43 94 LUAD TCGA-91-6836 FAIM2 SNP Missense_Mutation 12 50294991 C G 30 76 BRCA TCGA-A8-A06O FAIM2 SNP Silent 12 50291851 G A 40 43 CRC TCGA-AA-3845 FAIM2 SNP Missense_Mutation 12 50264399 C T 31 78 CRC TCGA-AA-A01R FAIM2 SNP Missense_Mutation 12 50284471 C T 19 49 CRC TCGA-AA-A022 FAIM2 SNP Missense_Mutation 12 50294951 G A 38 76 AML TCGA-AB-2816 FAIM2 SNP Missense_Mutation 12 50282962 G C 38 35 KIRC TCGA-AK-3434 FAIM2 SNP Missense_Mutation 12 50284501 G T 46 55 UCEC TCGA-AP-A051 FAIM2 SNP Missense_Mutation 12 50264311 C A 28 72 UCEC TCGA-AP-A051 FAIM2 SNP Missense_Mutation 12 50283284 C T 19 36 UCEC TCGA-AP-A0LM FAIM2 SNP Missense_Mutation 12 50295007 C A 24 58 UCEC TCGA-BS-A0TA FAIM2 SNP Silent 12 50284472 G A 39 63