ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-Ls420 MAN1B1 SNP Missense_Mutation 9 139995473 G T 41 65 ESO ESO-2143 MAN1B1 SNP Missense_Mutation 9 139994231 G A 45 95 ESO ESO-774 MAN1B1 SNP Missense_Mutation 9 139981464 G C 37 51 MEL MEL-JWCI-WGS-25 MAN1B1 SNP Missense_Mutation 9 139990824 C T 30 19 MEL MEL-Ma-Mel-48 MAN1B1 SNP Silent 9 140001848 C T 31 50 OV TCGA-04-1367 MAN1B1 SNP Silent 9 139983342 A T 9 74 LUAD TCGA-05-4396 MAN1B1 SNP Silent 9 140001842 C A 23 46 LUAD TCGA-17-Z010 MAN1B1 SNP Missense_Mutation 9 139982623 G T 45 52 LUSC TCGA-18-3414 MAN1B1 SNP Silent 9 140002866 C T 29 61 LUAD TCGA-38-4625 MAN1B1 SNP Missense_Mutation 9 140001223 G T 48 80 CRC TCGA-AA-3555 MAN1B1 SNP Silent 9 140001201 C T 23 25 CRC TCGA-AA-3949 MAN1B1 SNP Missense_Mutation 9 139994310 T C 51 88 AML TCGA-AB-2854 MAN1B1 SNP Missense_Mutation 9 139983453 C T 29 67 UCEC TCGA-AP-A056 MAN1B1 SNP Missense_Mutation 9 140002967 A G 10 69 UCEC TCGA-AP-A0LM MAN1B1 SNP Missense_Mutation 9 139982566 C A 32 53 UCEC TCGA-AP-A0LM MAN1B1 SNP Missense_Mutation 9 139982614 A G 5 63 UCEC TCGA-AP-A0LM MAN1B1 SNP Missense_Mutation 9 139990703 C G 17 49 UCEC TCGA-AP-A0LM MAN1B1 SNP Missense_Mutation 9 140002859 C T 32 96 UCEC TCGA-AP-A0LM MAN1B1 SNP Missense_Mutation 9 140002908 G T 33 61 KIRC TCGA-B0-4823 MAN1B1 SNP Silent 9 140002045 C T 27 46 HNSC TCGA-BA-4074 MAN1B1 SNP Splice_Site 9 139990687 A C 7 73 BLCA TCGA-BT-A3PH MAN1B1 SNP Missense_Mutation 9 140003028 C G 32 65 BLCA TCGA-BT-A3PJ MAN1B1 SNP Missense_Mutation 9 139981500 T A 58 50 HNSC TCGA-CN-4725 MAN1B1 SNP Silent 9 139995566 C G 24 77 HNSC TCGA-CV-5439 MAN1B1 SNP Missense_Mutation 9 139981560 A G 8 55 HNSC TCGA-CV-7425 MAN1B1 SNP Nonsense_Mutation 9 139994165 C T 21 82 UCEC TCGA-D1-A103 MAN1B1 SNP Missense_Mutation 9 139996044 G A 37 95 BLCA TCGA-DK-A3IN MAN1B1 SNP Missense_Mutation 9 140002847 C G 31 68 BLCA TCGA-DK-A3IN MAN1B1 SNP Silent 9 140002885 C G 29 48 BRCA TCGA-E2-A159 MAN1B1 SNP Missense_Mutation 9 139995528 G C 45 99 BRCA TCGA-E9-A1NG MAN1B1 SNP Missense_Mutation 9 139996024 A C 6 70