ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CW243 MAN1A1 SNP Missense_Mutation 6 119669923 C A 23 59 DLBCL DLBCL-Ls2367 MAN1A1 SNP Missense_Mutation 6 119669840 C G 26 94 DLBCL DLBCL-MAYO_DLBCL_234 MAN1A1 SNP Missense_Mutation 6 119526043 T C 49 66 LUAD LUAD-CHTN-MAD06-00668 MAN1A1 SNP Missense_Mutation 6 119611895 G A 40 89 LUAD LUAD-RT-S01477 MAN1A1 SNP Missense_Mutation 6 119569468 G A 45 71 MEL MEL-JWCI-27 MAN1A1 SNP Nonsense_Mutation 6 119569513 G A 37 86 MEL MEL-JWCI-WGS-1 MAN1A1 SNP Splice_Site 6 119511049 C T 24 100 MEL MEL-JWCI-WGS-12 MAN1A1 SNP Silent 6 119514975 C T 21 46 MEL MEL-JWCI-WGS-12 MAN1A1 SNP Missense_Mutation 6 119669708 C T 30 56 MEL MEL-JWCI-WGS-13 MAN1A1 SNP Missense_Mutation 6 119669858 G A 39 64 MEL MEL-JWCI-WGS-18 MAN1A1 SNP Missense_Mutation 6 119510940 C T 22 87 MEL MEL-JWCI-WGS-6 MAN1A1 SNP Missense_Mutation 6 119510939 C T 22 100 MEL MEL-Ma-Mel-35 MAN1A1 SNP Silent 6 119510944 G A 37 53 MEL MEL-Ma-Mel-53 MAN1A1 DNP Missense_Mutation 6 119511027 GG AA 39 77 MEL MEL-Ma-Mel-62 MAN1A1 SNP Missense_Mutation 6 119569512 C T 31 73 MEL MEL-Ma-Mel-65 MAN1A1 SNP Missense_Mutation 6 119623210 C T 29 94 MEL MEL-Ma-Mel-79 MAN1A1 SNP Silent 6 119525945 T A 62 53 MM MM-0322 MAN1A1 SNP Missense_Mutation 6 119509712 A C 1 93 MM MM-0335 MAN1A1 SNP Splice_Site_SNP 6 119623269 C A 24 94 OV TCGA-09-1661 MAN1A1 SNP Missense_Mutation 6 119526032 G C 36 57 GBM TCGA-19-2620 MAN1A1 SNP Missense_Mutation 6 119669897 C G 30 58 LUSC TCGA-33-4586 MAN1A1 SNP Missense_Mutation 6 119669750 G T 47 51 LUSC TCGA-37-5819 MAN1A1 SNP Missense_Mutation 6 119510840 T C 49 91 LUAD TCGA-55-1594 MAN1A1 INS Frame_Shift_Ins 6 119510935 - C 46 57 LUSC TCGA-66-2787 MAN1A1 SNP Missense_Mutation 6 119514988 T A 58 65 LUSC TCGA-66-2800 MAN1A1 SNP Missense_Mutation 6 119525941 G C 43 71 LUAD TCGA-75-5125 MAN1A1 SNP Silent 6 119670168 C A 26 49 CRC TCGA-A6-2672 MAN1A1 SNP Missense_Mutation 6 119515009 A G 7 92 BRCA TCGA-A8-A09R MAN1A1 SNP Silent 6 119569483 A G 4 68 CRC TCGA-AA-3715 MAN1A1 SNP Missense_Mutation 6 119501033 A G 11 90 CRC TCGA-AA-3845 MAN1A1 SNP Missense_Mutation 6 119510862 C T 25 87 CRC TCGA-AA-3955 MAN1A1 SNP Missense_Mutation 6 119623194 C G 32 94 CRC TCGA-AA-A01R MAN1A1 SNP Silent 6 119510998 G A 37 47 CRC TCGA-AG-A002 MAN1A1 SNP Nonsense_Mutation 6 119510835 G A 37 75 BRCA TCGA-AO-A124 MAN1A1 SNP Missense_Mutation 6 119501033 A G 11 90 UCEC TCGA-AP-A051 MAN1A1 SNP Missense_Mutation 6 119510928 C T 27 100 UCEC TCGA-AP-A056 MAN1A1 SNP Missense_Mutation 6 119511012 C T 23 100 UCEC TCGA-AX-A0J1 MAN1A1 SNP Missense_Mutation 6 119509656 G A 40 70 UCEC TCGA-B5-A11E MAN1A1 SNP Missense_Mutation 6 119509653 G A 42 100 UCEC TCGA-B5-A11E MAN1A1 SNP Missense_Mutation 6 119511012 C T 23 100 UCEC TCGA-BS-A0TJ MAN1A1 SNP Missense_Mutation 6 119510891 T C 63 69 UCEC TCGA-BS-A0UF MAN1A1 SNP Silent 6 119510929 G A 37 61 UCEC TCGA-BS-A0UJ MAN1A1 SNP Missense_Mutation 6 119628150 T C 64 73 UCEC TCGA-BS-A0UV MAN1A1 SNP Missense_Mutation 6 119525969 A T 13 52 BLCA TCGA-BT-A3PK MAN1A1 SNP Missense_Mutation 6 119669755 T C 55 57 KIRC TCGA-CJ-5677 MAN1A1 DEL Frame_Shift_Del 6 119522461 A - 13 90 HNSC TCGA-CR-7373 MAN1A1 SNP Silent 6 119501047 G A 38 38 UCEC TCGA-D1-A103 MAN1A1 SNP Silent 6 119501047 G A 38 38 UCEC TCGA-D1-A103 MAN1A1 SNP Missense_Mutation 6 119509728 G T 44 100 UCEC TCGA-D1-A103 MAN1A1 SNP Missense_Mutation 6 119522442 G A 43 98 UCEC TCGA-D1-A103 MAN1A1 SNP Missense_Mutation 6 119623164 C A 32 63 UCEC TCGA-D1-A16I MAN1A1 SNP Missense_Mutation 6 119628109 T G 64 85 UCEC TCGA-D1-A17Q MAN1A1 SNP Missense_Mutation 6 119669881 A G 7 51 BLCA TCGA-DK-A1AC MAN1A1 SNP Missense_Mutation 6 119669855 C T 31 69 KIRC TCGA-DV-5566 MAN1A1 SNP Missense_Mutation 6 119623209 T G 62 60