ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-Ls2367 MEPCE SNP Missense_Mutation 7 100028129 A G 1 81 MEL ME011 MEPCE SNP Missense_Mutation 7 100028633 C T 22 78 MEL ME032 MEPCE SNP Missense_Mutation 7 100028111 G A 41 74 MEL MEL-JWCI-WGS-12 MEPCE SNP Missense_Mutation 7 100028203 G A 43 90 LUAD TCGA-05-4396 MEPCE SNP Splice_Site 7 100028652 G T 35 64 LUAD TCGA-05-4396 MEPCE SNP Silent 7 100028722 C A 23 67 LUSC TCGA-18-3409 MEPCE SNP Missense_Mutation 7 100028584 C T 18 61 LUSC TCGA-18-3409 MEPCE SNP Missense_Mutation 7 100028585 C T 22 67 LUSC TCGA-22-5473 MEPCE SNP Silent 7 100029210 C T 30 60 LUAD TCGA-44-3919 MEPCE DEL Frame_Shift_Del 7 100030533 TGCCCTCAGGGTAATTATG - 63 50 LUAD TCGA-49-4514 MEPCE SNP Missense_Mutation 7 100028300 C T 23 90 LUSC TCGA-66-2767 MEPCE SNP Silent 7 100028427 G A 42 51 BRCA TCGA-A2-A0CQ MEPCE SNP Silent 7 100028415 T A 55 59 CRC TCGA-AA-A00A MEPCE SNP Missense_Mutation 7 100030692 C T 19 64 AML TCGA-AB-2806 MEPCE SNP Missense_Mutation 7 100028398 G A 46 65 CRC TCGA-AG-A002 MEPCE SNP Missense_Mutation 7 100030747 G T 33 79 CRC TCGA-AG-A00Y MEPCE INS Frame_Shift_Ins 7 100030612 - G 54 85 UCEC TCGA-AP-A059 MEPCE SNP Missense_Mutation 7 100028155 C T 27 60 UCEC TCGA-AP-A059 MEPCE SNP Missense_Mutation 7 100028423 A C 3 68 UCEC TCGA-AP-A0LM MEPCE SNP Missense_Mutation 7 100028872 C T 27 47 UCEC TCGA-AP-A0LM MEPCE SNP Missense_Mutation 7 100029074 G A 39 52 KIRC TCGA-B2-4098 MEPCE SNP Missense_Mutation 7 100031142 T A 57 70 UCEC TCGA-BG-A18B MEPCE SNP Missense_Mutation 7 100031137 C A 24 89 UCEC TCGA-BS-A0UF MEPCE SNP Silent 7 100028961 G A 36 53 UCEC TCGA-BS-A0UF MEPCE SNP Missense_Mutation 7 100030735 C T 31 72 UCEC TCGA-BS-A0UV MEPCE SNP Missense_Mutation 7 100029194 G A 37 58 UCEC TCGA-BS-A0UV MEPCE SNP Missense_Mutation 7 100030674 C T 23 48 UCEC TCGA-D1-A103 MEPCE SNP Missense_Mutation 7 100028915 G A 38 72 UCEC TCGA-D1-A15X MEPCE SNP Missense_Mutation 7 100029091 C T 23 71 BRCA TCGA-D8-A1JN MEPCE SNP Missense_Mutation 7 100030928 G C 33 76 BLCA TCGA-DK-A3IS MEPCE SNP Missense_Mutation 7 100028615 G A 35 68