ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-005 FITM2 SNP Missense_Mutation 20 42935360 C T 23 65 LUAD LUAD-NYU284 FITM2 SNP Silent 20 42935673 C A 21 68 PRAD PR-03-3125 FITM2 SNP Silent 20 42935850 C T 19 47 BRCA TCGA-A8-A07J FITM2 SNP Missense_Mutation 20 42935409 G T 36 57 UCEC TCGA-AP-A0LM FITM2 SNP Missense_Mutation 20 42935515 C T 31 75 KIRC TCGA-B0-4848 FITM2 SNP Missense_Mutation 20 42935674 A T 7 60 UCEC TCGA-B5-A0K9 FITM2 SNP Missense_Mutation 20 42935630 G T 47 45 BRCA TCGA-BH-A0B0 FITM2 SNP Silent 20 42935837 G A 33 68 KIRC TCGA-CJ-4894 FITM2 SNP Nonsense_Mutation 20 42935614 C T 21 98 HNSC TCGA-CV-7248 FITM2 SNP Missense_Mutation 20 42935681 G A 43 61 HNSC TCGA-DQ-5624 FITM2 SNP Silent 20 42935537 G A 34 51 BLCA TCGA-GV-A3QI FITM2 SNP Missense_Mutation 20 42935833 G C 35 99