ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-F00365 E2F5 SNP Splice_site 8 86114489 G T 41 89 LUAD LUAD_E00565 E2F5 SNP Silent 8 86114438 C G 32 58 MM MM-0638 E2F5 SNP Missense_Mutation 8 86126018 C T 23 80 LUAD TCGA-05-4398 E2F5 SNP Silent 8 86124414 C T 29 60 OV TCGA-09-0369 E2F5 SNP Missense_Mutation 8 86125997 T A 54 73 LUSC TCGA-18-4083 E2F5 SNP Missense_Mutation 8 86118434 G A 33 99 LUSC TCGA-33-6737 E2F5 SNP Missense_Mutation 8 86121488 G A 48 77 KIRC TCGA-A3-3376 E2F5 SNP Missense_Mutation 8 86119690 C A 32 69 BRCA TCGA-A8-A06N E2F5 SNP Missense_Mutation 8 86121476 G A 40 85 CRC TCGA-AA-3693 E2F5 DEL Splice_site 8 86119724 G - 47 75 CRC TCGA-AA-3947 E2F5 SNP Nonsense_Mutation 8 86121614 C T 25 73 UCEC TCGA-AP-A051 E2F5 SNP Splice_Site 8 86114381 G T 35 100 UCEC TCGA-AP-A056 E2F5 SNP Missense_Mutation 8 86121608 G A 42 49 UCEC TCGA-AX-A05Z E2F5 SNP Missense_Mutation 8 86121394 G T 33 78 UCEC TCGA-B5-A0JY E2F5 SNP Missense_Mutation 8 86089855 A G 7 71 UCEC TCGA-B5-A11H E2F5 SNP Missense_Mutation 8 86121540 T C 59 49 KIRC TCGA-BP-4781 E2F5 SNP Silent 8 86118418 C A 24 50 HNSC TCGA-CN-5360 E2F5 SNP Splice_Site 8 86114380 A T 7 92 HNSC TCGA-CQ-5331 E2F5 SNP Missense_Mutation 8 86114424 G A 45 100 HNSC TCGA-CV-6948 E2F5 SNP Missense_Mutation 8 86121536 C G 30 67 UCEC TCGA-D1-A167 E2F5 SNP Missense_Mutation 8 86118439 C T 32 59 UCEC TCGA-D1-A17Q E2F5 SNP Splice_site 8 86115490 G T 33 58 UCEC TCGA-D1-A17Q E2F5 SNP Nonsense_Mutation 8 86119719 G T 33 85 HNSC TCGA-D6-6516 E2F5 SNP Missense_Mutation 8 86114445 G A 43 100 BLCA TCGA-DK-A2I4 E2F5 SNP Missense_Mutation 8 86121423 C T 29 86 CARC Carc-Thirlwell3 E2F5 SNP Missense_Mutation 8 86126012 C A 24 93