ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-045 PGM2L1 SNP Nonsense_Mutation 11 74053656 A T 2 60 HNSC HN_62671 PGM2L1 SNP Missense 11 74062457 C T 21 58 MEL MEL-JWCI-WGS-1 PGM2L1 SNP Missense_Mutation 11 74085522 G A 37 62 MEL MEL-Ma-Mel-36 PGM2L1 SNP Missense_Mutation 11 74058339 A T 1 61 MM MM-0489 PGM2L1 SNP Silent 11 74058331 C T 22 24 PRAD PR-08-556 PGM2L1 SNP Silent 11 74109168 C G 25 57 LUAD TCGA-05-4396 PGM2L1 SNP Missense_Mutation 11 74082789 C A 23 89 LUAD TCGA-05-4424 PGM2L1 SNP Missense_Mutation 11 74053997 C T 29 96 OV TCGA-13-1510 PGM2L1 SNP Missense_Mutation 11 74047745 C G 32 53 LUAD TCGA-17-Z051 PGM2L1 SNP Missense_Mutation 11 74054407 T G 64 49 LUAD TCGA-17-Z058 PGM2L1 SNP Missense_Mutation 11 74053691 C A 21 92 LUSC TCGA-18-3414 PGM2L1 SNP Nonsense_Mutation 11 74062614 C T 21 96 LUSC TCGA-22-5491 PGM2L1 SNP Missense_Mutation 11 74057825 G A 42 92 OV TCGA-24-1463 PGM2L1 SNP Silent 11 74056676 G A 45 83 LUSC TCGA-33-4566 PGM2L1 SNP Silent 11 74047787 T C 57 50 LUSC TCGA-33-4583 PGM2L1 SNP Missense_Mutation 11 74053659 C G 17 44 LUAD TCGA-50-6594 PGM2L1 SNP Missense_Mutation 11 74049567 C A 30 96 LUSC TCGA-70-6723 PGM2L1 SNP Silent 11 74049611 T C 51 33 LUSC TCGA-85-6560 PGM2L1 SNP Silent 11 74054399 T C 56 60 UCEC TCGA-A5-A0VP PGM2L1 SNP Missense_Mutation 11 74058231 C T 19 97 AML TCGA-AB-2833 PGM2L1 SNP Missense_Mutation 11 74049537 T A 54 88 CRC TCGA-AG-A002 PGM2L1 SNP Nonsense_Mutation 11 74047777 C A 32 76 CRC TCGA-AG-A002 PGM2L1 SNP Missense_Mutation 11 74056556 T G 64 63 UCEC TCGA-AJ-A23M PGM2L1 SNP Splice_Site 11 74058192 C A 18 97 UCEC TCGA-AP-A056 PGM2L1 SNP Missense_Mutation 11 74053588 G T 47 92 UCEC TCGA-AP-A0LM PGM2L1 SNP Silent 11 74081995 T C 56 77 UCEC TCGA-AX-A0J0 PGM2L1 SNP Missense_Mutation 11 74058371 G A 37 56 BRCA TCGA-B6-A0X1 PGM2L1 SNP Missense_Mutation 11 74058348 G T 46 96 HNSC TCGA-BB-7861 PGM2L1 SNP Silent 11 74058232 G A 39 39 UCEC TCGA-BG-A0MQ PGM2L1 SNP Missense_Mutation 11 74082813 C T 26 76 BRCA TCGA-BH-A18P PGM2L1 SNP Silent 11 74062496 C G 29 61 KIRC TCGA-BP-4340 PGM2L1 SNP Splice_Site 11 74081946 C T 20 83 UCEC TCGA-BS-A0U8 PGM2L1 SNP Missense_Mutation 11 74056576 C T 28 64 UCEC TCGA-BS-A0UF PGM2L1 SNP Nonsense_Mutation 11 74056611 G T 45 92 UCEC TCGA-BS-A0UF PGM2L1 SNP Silent 11 74082761 G A 42 60 BLCA TCGA-BT-A3PH PGM2L1 SNP Missense_Mutation 11 74109127 G A 40 63 HNSC TCGA-CN-4723 PGM2L1 SNP Missense_Mutation 11 74053568 C G 25 52 HNSC TCGA-CV-7427 PGM2L1 SNP Silent 11 74056565 G C 33 72 UCEC TCGA-D1-A0ZO PGM2L1 SNP Missense_Mutation 11 74056662 A G 5 87 UCEC TCGA-D1-A16Y PGM2L1 SNP Missense_Mutation 11 74056590 T C 60 58 BLCA TCGA-DK-A1AF PGM2L1 SNP Silent 11 74056622 C T 32 58 BLCA TCGA-FD-A3NA PGM2L1 SNP Missense_Mutation 11 74053678 G A 45 70