ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MM MM-0644 TRAM1 SNP Silent 8 71487191 C T 30 51 LUSC TCGA-21-1070 TRAM1 SNP Missense_Mutation 8 71520391 C A 28 84 OV TCGA-24-2281 TRAM1 SNP Missense_Mutation 8 71499191 C G 17 78 GBM TCGA-28-5220 TRAM1 DEL Splice_Site 8 71510232 TCGCCTGTTAATTTTCTAAAAATAA - 62 55 LUAD TCGA-35-5375 TRAM1 SNP Missense_Mutation 8 71510383 C G 32 100 LUAD TCGA-44-2656 TRAM1 SNP Missense_Mutation 8 71512306 T A 56 56 LUAD TCGA-49-6767 TRAM1 SNP Missense_Mutation 8 71495976 G A 33 99 LUSC TCGA-60-2719 TRAM1 SNP Missense_Mutation 8 71506818 T C 52 61 LUAD TCGA-75-5125 TRAM1 SNP Missense_Mutation 8 71520431 C T 26 84 LUSC TCGA-85-6561 TRAM1 SNP Missense_Mutation 8 71495456 G A 44 77 KIRC TCGA-A3-3387 TRAM1 SNP Splice_site 8 71508498 G A 40 83 UCEC TCGA-A5-A0GP TRAM1 SNP Silent 8 71512312 C T 23 52 CRC TCGA-AA-3811 TRAM1 SNP Nonsense_Mutation 8 71510234 G A 38 71 CRC TCGA-AA-3984 TRAM1 SNP Missense_Mutation 8 71495488 C T 31 99 CRC TCGA-AA-A00N TRAM1 SNP Silent 8 71520395 G A 34 59 CRC TCGA-AG-A002 TRAM1 SNP Silent 8 71520329 G A 34 69 UCEC TCGA-B5-A11J TRAM1 SNP Splice_site 8 71508498 G A 40 83 UCEC TCGA-BG-A0VZ TRAM1 SNP Missense_Mutation 8 71495485 C A 24 86 BLCA TCGA-BT-A3PJ TRAM1 SNP Splice_Site 8 71510491 C T 32 87 HNSC TCGA-CQ-6225 TRAM1 SNP Missense_Mutation 8 71487192 C T 23 81 HNSC TCGA-CR-7379 TRAM1 SNP Missense_Mutation 8 71520380 C T 19 47 BLCA TCGA-FD-A3B6 TRAM1 SNP Missense_Mutation 8 71520314 C G 29 76 BLCA TCGA-GD-A2C5 TRAM1 SNP Silent 8 71508503 C G 29 52 HNSC TCGA-HL-7533 TRAM1 SNP Silent 8 71520408 C T 32 69