ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-045 MAN2A1 SNP Missense_Mutation 5 109153073 A T 2 54 ESO ESO-164 MAN2A1 SNP Missense_Mutation 5 109091073 G A 44 95 HNSC HN_00122 MAN2A1 SNP Splice_site 5 109200738 T C 59 53 LUAD LUAD-D01603 MAN2A1 SNP Nonsense_Mutation 5 109178037 G T 35 95 LUAD LUAD-RT-S01711 MAN2A1 SNP Nonsense_Mutation 5 109110646 C T 29 99 MEL ME002 MAN2A1 SNP Missense_Mutation 5 109110535 C T 31 99 MEL MEL-JWCI-WGS-6 MAN2A1 SNP Silent 5 109049367 C T 29 58 NB NB-0478 MAN2A1 SNP Missense_Mutation 5 109159532 A T 8 51 NB NB-3180 MAN2A1 SNP Silent 5 109103301 C T 32 78 LUAD TCGA-05-4396 MAN2A1 SNP Missense_Mutation 5 109103257 G T 47 100 LUAD TCGA-05-4396 MAN2A1 SNP Missense_Mutation 5 109153042 C A 23 68 OV TCGA-13-0714 MAN2A1 SNP Missense_Mutation 5 109190892 T A 62 72 LUAD TCGA-17-Z009 MAN2A1 SNP Missense_Mutation 5 109117165 G T 35 54 OV TCGA-24-2289 MAN2A1 SNP Silent 5 109103354 T C 61 52 LUSC TCGA-33-4583 MAN2A1 SNP Missense_Mutation 5 109103254 G T 42 87 LUSC TCGA-34-2596 MAN2A1 SNP Silent 5 109106207 C T 22 50 LUSC TCGA-34-5234 MAN2A1 SNP Missense_Mutation 5 109155491 G C 41 51 LUAD TCGA-35-3621 MAN2A1 SNP Splice_site 5 109202698 G A 45 88 LUSC TCGA-37-4133 MAN2A1 SNP Missense_Mutation 5 109190950 T C 56 58 LUSC TCGA-39-5016 MAN2A1 SNP Missense_Mutation 5 109181686 G T 35 97 LUAD TCGA-44-2656 MAN2A1 SNP Silent 5 109117174 G C 37 48 LUAD TCGA-44-5645 MAN2A1 SNP Missense_Mutation 5 109091091 A G 14 56 LUAD TCGA-49-6743 MAN2A1 SNP Missense_Mutation 5 109183385 G A 33 97 LUAD TCGA-49-6744 MAN2A1 SNP Missense_Mutation 5 109110522 G T 36 60 LUAD TCGA-50-6590 MAN2A1 SNP Missense_Mutation 5 109051935 T C 56 72 LUAD TCGA-50-6590 MAN2A1 SNP Missense_Mutation 5 109065175 G T 47 100 LUAD TCGA-64-5781 MAN2A1 SNP Missense_Mutation 5 109178149 T G 53 74 LUSC TCGA-66-2792 MAN2A1 SNP Missense_Mutation 5 109181611 G T 48 59 LUAD TCGA-75-5126 MAN2A1 SNP Missense_Mutation 5 109155485 A G 12 46 LUAD TCGA-91-6829 MAN2A1 SNP Missense_Mutation 5 109051926 C T 24 100 UCEC TCGA-A5-A0GH MAN2A1 SNP Silent 5 109049313 C T 29 55 UCEC TCGA-A5-A0GH MAN2A1 SNP Silent 5 109181688 G T 43 37 UCEC TCGA-A5-A0GP MAN2A1 SNP Missense_Mutation 5 109190857 C T 31 91 BRCA TCGA-A8-A08X MAN2A1 SNP Silent 5 109091135 T C 50 55 CRC TCGA-AA-3516 MAN2A1 SNP Missense_Mutation 5 109120531 C T 25 64 CRC TCGA-AA-3516 MAN2A1 SNP Missense_Mutation 5 109159443 C T 23 51 CRC TCGA-AA-3525 MAN2A1 SNP Silent 5 109106066 T G 55 56 CRC TCGA-AA-3976 MAN2A1 SNP Missense_Mutation 5 109125208 A G 13 55 CRC TCGA-AA-A004 MAN2A1 SNP Missense_Mutation 5 109117197 A T 12 91 CRC TCGA-AA-A010 MAN2A1 SNP Missense_Mutation 5 109120470 G A 38 82 CRC TCGA-AA-A01Q MAN2A1 SNP Missense_Mutation 5 109152979 T A 56 82 CRC TCGA-AA-A01R MAN2A1 SNP Missense_Mutation 5 109106146 G A 46 100 CRC TCGA-AA-A02Y MAN2A1 SNP Missense_Mutation 5 109065129 C T 19 56 CRC TCGA-AG-3581 MAN2A1 SNP Missense_Mutation 5 109049312 T A 58 83 CRC TCGA-AG-3892 MAN2A1 SNP Missense_Mutation 5 109200797 C T 31 64 CRC TCGA-AG-A002 MAN2A1 SNP Missense_Mutation 5 109155562 C T 31 46 CRC TCGA-AG-A002 MAN2A1 SNP Missense_Mutation 5 109156017 C A 24 78 KIRC TCGA-AK-3434 MAN2A1 SNP Missense_Mutation 5 109049281 A G 13 83 UCEC TCGA-AP-A051 MAN2A1 SNP Missense_Mutation 5 109049264 G A 40 77 UCEC TCGA-AP-A051 MAN2A1 SNP Missense_Mutation 5 109106077 T G 52 93 UCEC TCGA-AP-A056 MAN2A1 SNP Missense_Mutation 5 109110612 G T 33 57 UCEC TCGA-AP-A059 MAN2A1 SNP Silent 5 109106195 C A 24 55 UCEC TCGA-AP-A059 MAN2A1 SNP Missense_Mutation 5 109155562 C T 31 46 UCEC TCGA-AP-A059 MAN2A1 SNP Missense_Mutation 5 109178108 T G 64 59 UCEC TCGA-AP-A0LM MAN2A1 SNP Missense_Mutation 5 109152994 C A 24 89 UCEC TCGA-AP-A0LM MAN2A1 SNP Silent 5 109178114 T G 55 50 UCEC TCGA-AP-A0LM MAN2A1 SNP Silent 5 109202609 C A 24 57 BRCA TCGA-AR-A0TP MAN2A1 SNP Missense_Mutation 5 109202637 A G 9 81 BRCA TCGA-AR-A0TU MAN2A1 SNP Missense_Mutation 5 109200756 A G 4 62 UCEC TCGA-AX-A05Z MAN2A1 SNP Nonsense_Mutation 5 109183456 C T 31 82 UCEC TCGA-AX-A0IW MAN2A1 SNP Silent 5 109103384 G A 47 64 UCEC TCGA-AX-A0J0 MAN2A1 SNP Missense_Mutation 5 109106067 G T 48 68 UCEC TCGA-AX-A0J1 MAN2A1 SNP Missense_Mutation 5 109155943 G A 44 60 KIRC TCGA-B0-5696 MAN2A1 SNP Missense_Mutation 5 109110522 G C 36 60 UCEC TCGA-B5-A0K9 MAN2A1 SNP Missense_Mutation 5 109153095 G A 38 88 UCEC TCGA-B5-A11E MAN2A1 SNP Missense_Mutation 5 109190857 C T 31 91 UCEC TCGA-B5-A11N MAN2A1 SNP Missense_Mutation 5 109155562 C T 31 46 UCEC TCGA-BG-A0LX MAN2A1 SNP Silent 5 109117133 C T 28 48 UCEC TCGA-BG-A18B MAN2A1 SNP Missense_Mutation 5 109117235 A G 11 91 BRCA TCGA-BH-A0C1 MAN2A1 SNP Silent 5 109183450 C T 32 55 UCEC TCGA-BS-A0TC MAN2A1 SNP Silent 5 109152986 C T 32 54 UCEC TCGA-BS-A0TC MAN2A1 SNP Missense_Mutation 5 109190936 C A 32 52 UCEC TCGA-BS-A0TE MAN2A1 SNP Missense_Mutation 5 109155529 G T 35 54 UCEC TCGA-BS-A0UF MAN2A1 SNP Nonsense_Mutation 5 109091037 G T 33 55 UCEC TCGA-BS-A0UF MAN2A1 SNP Missense_Mutation 5 109120458 C A 32 82 UCEC TCGA-BS-A0UF MAN2A1 SNP Missense_Mutation 5 109120509 C A 32 74 UCEC TCGA-BS-A0UF MAN2A1 SNP Missense_Mutation 5 109190985 T G 50 51 HNSC TCGA-CN-4723 MAN2A1 SNP Missense_Mutation 5 109181672 C G 32 97 HNSC TCGA-CN-5359 MAN2A1 SNP Missense_Mutation 5 109153015 C T 31 89 HNSC TCGA-CN-5374 MAN2A1 SNP Silent 5 109152986 C G 32 54 UCEC TCGA-D1-A103 MAN2A1 SNP Missense_Mutation 5 109117124 T G 64 91 UCEC TCGA-D1-A103 MAN2A1 SNP Silent 5 109181640 C A 30 56 UCEC TCGA-D1-A16X MAN2A1 SNP Missense_Mutation 5 109120509 C A 32 74 UCEC TCGA-D1-A17Q MAN2A1 SNP Silent 5 109103261 T C 53 50 BRCA TCGA-D8-A140 MAN2A1 SNP Missense_Mutation 5 109091068 G T 42 95 BLCA TCGA-DK-A1AC MAN2A1 SNP Nonsense_Mutation 5 109202634 C T 29 65 BLCA TCGA-DK-A3IN MAN2A1 SNP Missense_Mutation 5 109191017 G C 45 56 BLCA TCGA-FD-A3B4 MAN2A1 SNP Missense_Mutation 5 109026216 A G 14 65 BLCA TCGA-GV-A3JX MAN2A1 SNP Missense_Mutation 5 109026163 C G 32 60 CARC Carc-Asa8 MAN2A1 SNP Silent 5 109159486 G A 45 61