Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4248 |
| ensemblid | ENSG00000128268.12 |
| hgncid | 7046 |
| symbol | MGAT3 |
| name | beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase |
| refseq_nuc | NM_002409.5 |
| refseq_prot | NP_002400.3 |
| ensembl_nuc | ENST00000341184.7 |
| ensembl_prot | ENSP00000345270.6 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 39457012 |
| end | 39492194 |
| strand | + |
| ver | v1.2 |
| region | chr22:39457012-39492194 |
| region5000 | chr22:39452012-39497194 |
| regionname0 | MGAT3_chr22_39457012_39492194 |
| regionname5000 | MGAT3_chr22_39452012_39497194 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 533 | 303 | 95 | 74 | 70 | 18 | 44 | 40 | MGAT3_chr22_39452012_39497194 | MGAT3 | MKMRR others(528): Show |
chr22 | 39452012 | 39497194 |
| a0002 | 0/0 | 533 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MGAT3_chr22_39452012_39497194 | MGAT3 | MKMRR others(528): Show |
chr22 | 39452012 | 39497194 |
| a0003 | 0/0 | 533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | MKMRR others(528): Show |
chr22 | 39452012 | 39497194 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1599 | 245 | 72 | 71 | 45 | 15 | 40 | MGAT3_chr22_39452012_39497194 | MGAT3 | ATGAA others(1594): Show |
chr22 | 39452012 | 39497194 | ||
| a0001c0002 | 0/0 | 1599 | 46 | 20 | 3 | 20 | 0 | 3 | MGAT3_chr22_39452012_39497194 | MGAT3 | ATGAA others(1594): Show |
chr22 | 39452012 | 39497194 | ||
| a0001c0003 | 0/0 | 1599 | 4 | 0 | 0 | 1 | 2 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | ATGAA others(1594): Show |
chr22 | 39452012 | 39497194 | ||
| a0001c0004 | 0/0 | 1599 | 4 | 0 | 0 | 4 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ATGAA others(1594): Show |
chr22 | 39452012 | 39497194 | ||
| a0001c0005 | 0/0 | 1599 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ATGAA others(1594): Show |
chr22 | 39452012 | 39497194 | ||
| a0001c0007 | 0/0 | 1599 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ATGAA others(1594): Show |
chr22 | 39452012 | 39497194 | ||
| a0001c0008 | 0/0 | 1599 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ATGAA others(1594): Show |
chr22 | 39452012 | 39497194 | ||
| a0002c0006 | 0/0 | 1599 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ATGAA others(1594): Show |
chr22 | 39452012 | 39497194 | ||
| a0003c0009 | 0/0 | 1599 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ATGAA others(1594): Show |
chr22 | 39452012 | 39497194 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5393 | 145 | 28 | 47 | 34 | 12 | 23 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0002 | 0/0 | 5393 | 3 | 1 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0003 | 0/0 | 5393 | 22 | 10 | 3 | 1 | 0 | 8 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0004 | 1/0 | 5393 | 21 | 2 | 8 | 3 | 1 | 6 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0005 | 0/0 | 5393 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0006 | 0/0 | 5393 | 9 | 7 | 1 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0007 | 0/0 | 5392 | 7 | 7 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5387): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0008 | 0/0 | 5393 | 4 | 4 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0010 | 0/0 | 5393 | 3 | 3 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0011 | 0/0 | 5396 | 3 | 1 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5391): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0012 | 0/0 | 5393 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0013 | 0/0 | 5394 | 2 | 0 | 1 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5389): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0014 | 0/0 | 5393 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0017 | 0/0 | 5394 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5389): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0019 | 0/0 | 5393 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0020 | 0/0 | 5393 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0021 | 0/0 | 5392 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5387): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0022 | 0/0 | 5393 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0023 | 0/0 | 5393 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0024 | 0/0 | 5393 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0026 | 0/0 | 5394 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5389): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0027 | 0/0 | 5397 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5392): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0028 | 0/0 | 5393 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0029 | 0/0 | 5393 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0030 | 0/0 | 5393 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0031 | 0/0 | 5393 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0032 | 0/0 | 5393 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0033 | 0/0 | 5393 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0034 | 0/0 | 5393 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0035 | 0/0 | 5393 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0036 | 0/0 | 5393 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0038 | 0/0 | 5393 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0039 | 0/0 | 5393 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0001t0040 | 0/0 | 5393 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0002t0002 | 0/0 | 5393 | 31 | 8 | 2 | 18 | 0 | 3 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0002t0005 | 0/0 | 5393 | 11 | 11 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0002t0016 | 0/0 | 5393 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0002t0018 | 0/0 | 5393 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0002t0025 | 0/0 | 5393 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0002t0037 | 0/0 | 5393 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0003t0002 | 0/0 | 5393 | 4 | 0 | 0 | 1 | 2 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0004t0009 | 0/0 | 5393 | 4 | 0 | 0 | 4 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0005t0015 | 0/0 | 5393 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0007t0008 | 0/0 | 5393 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0001c0008t0001 | 0/0 | 5393 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0002c0006t0001 | 0/0 | 5393 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| a0003c0009t0003 | 0/0 | 5393 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | ACTCA others(5388): Show |
chr22 | 39452012 | 39497194 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 0 | 4 | 7 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 0 | 3 | 2 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0010 | 0/1 | 3 | 1 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0004g0003 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0004g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0004g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0004g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0006g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0006g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0007g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0007g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0008g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0008g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0010g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0010g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0010g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0011g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0011g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0011g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0012g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0012g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0013g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0013g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0014g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0014g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0017g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0019g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0020g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0021g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0022g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0023g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0024g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0026g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0027g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0028g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0029g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0030g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0031g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0032g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0033g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0034g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0035g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0036g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0038g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0039g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0001t0040g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0005g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0005g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0016g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0018g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0025g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0002t0037g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0004t0009g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0004t0009g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0005t0015g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0007t0008g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0001c0008t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0002c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0002c0006t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| a0003c0009t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00099 | hp2 | a0001 | c0008 | t0001 | g0002 | EUR | GBR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0227 | EUR | GBR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00280 | hp1 | a0001 | c0001 | t0024 | g0098 | EUR | FIN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | FIN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | FIN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00423 | hp1 | a0001 | c0001 | t0026 | g0037 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0034 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00609 | hp2 | a0001 | c0001 | t0035 | g0040 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00639 | hp1 | a0001 | c0001 | t0011 | g0065 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00639 | hp2 | a0001 | c0001 | t0012 | g0228 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0223 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00642 | hp2 | a0001 | c0001 | t0013 | g0027 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0232 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01081 | hp1 | a0001 | c0001 | t0040 | g0113 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01099 | hp2 | a0001 | c0001 | t0017 | g0003 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0231 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0117 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01167 | hp1 | a0001 | c0002 | t0018 | g0234 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01175 | hp1 | a0001 | c0001 | t0021 | g0212 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01243 | hp1 | a0001 | c0001 | t0022 | g0215 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0205 | AMR | PUR | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0226 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01496 | hp2 | a0001 | c0001 | t0012 | g0225 | AMR | CLM | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01515 | hp1 | a0001 | c0003 | t0002 | g0199 | EUR | IBS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | IBS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | IBS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0193 | EUR | IBS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01517 | hp1 | a0001 | c0003 | t0002 | g0198 | EUR | IBS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | IBS | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0109 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0213 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01934 | hp1 | a0001 | c0001 | t0011 | g0066 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01943 | hp1 | a0001 | c0001 | t0028 | g0195 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0158 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0094 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0220 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02129 | hp2 | a0001 | c0001 | t0033 | g0182 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0056 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0049 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CDX | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | CDX | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CDX | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CDX | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0201 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02258 | hp2 | a0003 | c0009 | t0003 | g0067 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | PEL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02451 | hp2 | a0001 | c0002 | t0005 | g0095 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0127 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0207 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02647 | hp1 | a0001 | c0001 | t0020 | g0233 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02647 | hp2 | a0001 | c0001 | t0036 | g0079 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0097 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02698 | hp2 | a0001 | c0001 | t0030 | g0186 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02717 | hp1 | a0001 | c0002 | t0005 | g0106 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0216 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0107 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0230 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0090 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0166 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02886 | hp1 | a0001 | c0002 | t0005 | g0105 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02895 | hp1 | a0001 | c0001 | t0014 | g0078 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0218 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0047 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02896 | hp2 | a0001 | c0001 | t0014 | g0076 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0221 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02922 | hp2 | a0001 | c0001 | t0010 | g0071 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02965 | hp1 | a0001 | c0002 | t0005 | g0015 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02965 | hp2 | a0001 | c0001 | t0038 | g0050 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0103 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0059 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02976 | hp1 | a0001 | c0001 | t0029 | g0062 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03041 | hp2 | a0001 | c0007 | t0008 | g0115 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03098 | hp1 | a0001 | c0002 | t0005 | g0118 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0217 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0214 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0244 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0142 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0235 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03486 | hp1 | a0001 | c0002 | t0016 | g0209 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03486 | hp2 | a0001 | c0002 | t0005 | g0016 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0131 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0128 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03516 | hp1 | a0001 | c0002 | t0005 | g0016 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03516 | hp2 | a0001 | c0001 | t0027 | g0030 | AFR | ESN | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0051 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03579 | hp2 | a0001 | c0002 | t0005 | g0015 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0224 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0028 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0229 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03831 | hp1 | a0001 | c0001 | t0023 | g0168 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03831 | hp2 | a0001 | c0001 | t0039 | g0179 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03927 | hp1 | a0001 | c0003 | t0002 | g0162 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0130 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0075 | AFR | YRI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | CHB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18906 | hp1 | a0001 | c0005 | t0015 | g0011 | AFR | YRI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | YRI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18952 | hp2 | a0001 | c0001 | t0031 | g0163 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18964 | hp2 | a0001 | c0004 | t0009 | g0009 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA18994 | hp2 | a0001 | c0002 | t0025 | g0092 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19007 | hp1 | a0002 | c0006 | t0001 | g0140 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19007 | hp2 | a0001 | c0004 | t0009 | g0009 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19009 | hp1 | a0001 | c0004 | t0009 | g0164 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19009 | hp2 | a0001 | c0002 | t0037 | g0173 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19011 | hp2 | a0001 | c0004 | t0009 | g0009 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | LWK | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | LWK | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19043 | hp2 | a0001 | c0001 | t0019 | g0236 | AFR | LWK | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19056 | hp2 | a0001 | c0003 | t0002 | g0161 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19075 | hp2 | a0001 | c0001 | t0034 | g0125 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19080 | hp2 | a0001 | c0001 | t0032 | g0135 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19090 | hp1 | a0001 | c0001 | t0013 | g0175 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19090 | hp2 | a0002 | c0006 | t0001 | g0001 | EAS | JPT | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19240 | hp1 | a0001 | c0001 | t0011 | g0030 | AFR | YRI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0108 | AFR | YRI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA20129 | hp1 | a0001 | c0005 | t0015 | g0011 | AFR | ASW | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0204 | AFR | ASW | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0222 | EUR | TSI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | TSI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | GIH | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0159 | SAS | GIH | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02486 | hp1 | a0001 | c0002 | t0005 | g0093 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0206 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02559 | hp1 | a0001 | c0002 | t0005 | g0200 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG02559 | hp2 | a0001 | c0002 | t0005 | g0238 | AFR | ACB | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | USA | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | USA | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | USA | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | USA | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0104 | AFR | LWK | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0132 | AFR | LWK | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0010 | REF | REF | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0237 | REF | REF | MGAT3_chr22_39452012_39497194 | MGAT3 | chr22 | 39452012 | 39497194 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39487544 | G | T | 1 | a0003 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.197G>T | p.Gly66Val | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 744/5394 | 197/1602 | 66/533 | chr22 | 39487544 | |||
| chr22:39487600 | C | T | 1 | a0002 | 2 | NA19007.hp1 NA19090.hp2 |
missense_variant | MODERATE | c.253C>T | p.Pro85Ser | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 800/5394 | 253/1602 | 85/533 | chr22 | 39487600 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39487599 | G | T | 1 | a0002c0006 | 2 | NA19007.hp1 NA19090.hp2 |
synonymous_variant | LOW | c.252G>T | p.Leu84Leu | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 799/5394 | 252/1602 | 84/533 | chr22 | 39487599 | |||
| chr22:39487731 | G | C | 2 | a0001c0002 a0001c0003 |
50 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
synonymous_variant | LOW | c.384G>C | p.Pro128Pro | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 931/5394 | 384/1602 | 128/533 | chr22 | 39487731 | |||
| chr22:39488274 | C | T | 1 | a0001c0004 | 4 | NA18964.hp2 NA19007.hp2 NA19009.hp1 others(1): Show |
synonymous_variant | LOW | c.927C>T | p.Pro309Pro | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1474/5394 | 927/1602 | 309/533 | chr22 | 39488274 | |||
| chr22:39488352 | C | G | 1 | a0001c0008 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.1005C>G | p.Gly335Gly | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1552/5394 | 1005/1602 | 335/533 | chr22 | 39488352 | |||
| chr22:39488388 | G | A | 1 | a0001c0005 | 2 | NA18906.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.1041G>A | p.Ser347Ser | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1588/5394 | 1041/1602 | 347/533 | chr22 | 39488388 | |||
| chr22:39488436 | A | G | 1 | a0001c0007 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.1089A>G | p.Ser363Ser | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1636/5394 | 1089/1602 | 363/533 | chr22 | 39488436 | |||
| chr22:39488937 | G | A | 1 | a0001c0003 | 4 | HG01515.hp1 HG01517.hp1 HG03927.hp1 others(1): Show |
synonymous_variant | LOW | c.1590G>A | p.Glu530Glu | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 2137/5394 | 1590/1602 | 530/533 | chr22 | 39488937 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39457185 | C | A | 1 | a0001c0002t0016 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-374C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/2 | 30163 | chr22 | 39457185 | ||||||
| chr22:39457244 | C | G | 1 | a0001c0001t0040 | 1 | HG01081.hp1 | 5_prime_UTR_variant | MODIFIER | c.-315C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/2 | 30104 | chr22 | 39457244 | ||||||
| chr22:39457253 | C | G | 1 | a0001c0001t0039 | 1 | HG03831.hp2 | 5_prime_UTR_variant | MODIFIER | c.-306C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/2 | 30095 | chr22 | 39457253 | ||||||
| chr22:39457308 | C | T | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(35): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-251C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/2 | chr22 | 39457308 | |||||||
| chr22:39457362 | T | G | 1 | a0001c0001t0023 | 1 | HG03831.hp1 | 5_prime_UTR_variant | MODIFIER | c.-197T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/2 | 29986 | chr22 | 39457362 | ||||||
| chr22:39457411 | G | C | 1 | a0001c0001t0024 | 1 | HG00280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-148G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/2 | 29937 | chr22 | 39457411 | ||||||
| chr22:39457458 | G | A | 2 | a0001c0001t0024 a0001c0002t0025 |
2 | HG00280.hp1 NA18994.hp2 |
5_prime_UTR_variant | MODIFIER | c.-101G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/2 | 29890 | chr22 | 39457458 | ||||||
| chr22:39457525 | C | T | 1 | a0001c0001t0022 | 1 | HG01243.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-34C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/2 | chr22 | 39457525 | |||||||
| chr22:39488982 | C | CG | 4 | a0001c0001t0013 a0001c0001t0017 a0001c0001t0026 others(1): Show |
5 | HG00423.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*38dupG | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 39 | INFO_REALIGN_3_PRIME | chr22 | 39488982 | |||||
| chr22:39489166 | G | T | 3 | a0001c0001t0011 a0001c0001t0027 a0001c0001t0038 |
5 | HG00639.hp1 HG01934.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*217G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 217 | chr22 | 39489166 | ||||||
| chr22:39489182 | C | T | 1 | a0001c0002t0037 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*233C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 233 | chr22 | 39489182 | ||||||
| chr22:39489250 | C | T | 3 | a0001c0001t0011 a0001c0001t0027 a0001c0001t0038 |
5 | HG00639.hp1 HG01934.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*301C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 301 | chr22 | 39489250 | ||||||
| chr22:39489552 | C | A | 1 | a0001c0001t0028 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*603C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 603 | chr22 | 39489552 | ||||||
| chr22:39489645 | G | A | 1 | a0001c0001t0029 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*696G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 696 | chr22 | 39489645 | ||||||
| chr22:39489719 | TG | T | 2 | a0001c0001t0007 a0001c0001t0021 |
8 | HG01175.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*771delG | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 771 | chr22 | 39489719 | ||||||
| chr22:39490052 | G | A | 2 | a0001c0001t0030 a0001c0001t0040 |
2 | HG01081.hp1 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1103G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1103 | chr22 | 39490052 | ||||||
| chr22:39490212 | C | G | 5 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0022 others(2): Show |
34 | HG00140.hp2 HG00642.hp1 HG01243.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1263C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1263 | chr22 | 39490212 | ||||||
| chr22:39490219 | C | G | 2 | a0001c0001t0020 a0001c0001t0036 |
2 | HG02647.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1270C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1270 | chr22 | 39490219 | ||||||
| chr22:39490226 | G | GCTT | 2 | a0001c0001t0011 a0001c0001t0027 |
4 | HG00639.hp1 HG01934.hp1 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1278_*1279insTTC | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1279 | INFO_REALIGN_3_PRIME | chr22 | 39490226 | |||||
| chr22:39490228 | A | C | 2 | a0001c0001t0011 a0001c0001t0027 |
4 | HG00639.hp1 HG01934.hp1 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1279A>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1279 | chr22 | 39490228 | ||||||
| chr22:39490364 | T | C | 1 | a0001c0001t0038 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1415T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1415 | chr22 | 39490364 | ||||||
| chr22:39490510 | G | A | 1 | a0001c0001t0031 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1561G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1561 | chr22 | 39490510 | ||||||
| chr22:39490528 | C | G | 4 | a0001c0001t0005 a0001c0001t0019 a0001c0002t0005 others(1): Show |
14 | HG01884.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1579C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1579 | chr22 | 39490528 | ||||||
| chr22:39490550 | G | A | 1 | a0001c0004t0009 | 4 | NA18964.hp2 NA19007.hp2 NA19009.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1601G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1601 | chr22 | 39490550 | ||||||
| chr22:39490633 | C | T | 1 | a0001c0001t0035 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1684C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1684 | chr22 | 39490633 | ||||||
| chr22:39490679 | G | A | 1 | a0001c0001t0032 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1730G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1730 | chr22 | 39490679 | ||||||
| chr22:39490745 | T | G | 1 | a0001c0001t0033 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1796T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 1796 | chr22 | 39490745 | ||||||
| chr22:39491062 | C | A | 1 | a0001c0001t0034 | 1 | NA19075.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2113C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 2113 | chr22 | 39491062 | ||||||
| chr22:39491207 | C | T | 4 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0021 others(1): Show |
12 | HG00639.hp2 HG01175.hp1 HG01496.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2258C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 2258 | chr22 | 39491207 | ||||||
| chr22:39491230 | G | A | 1 | a0001c0001t0010 | 3 | HG02818.hp1 HG02922.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2281G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 2281 | chr22 | 39491230 | ||||||
| chr22:39491537 | C | G | 12 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0011 others(9): Show |
29 | HG00639.hp1 HG00639.hp2 HG01496.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2588C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 2588 | chr22 | 39491537 | ||||||
| chr22:39491550 | G | C | 4 | a0001c0001t0005 a0001c0001t0019 a0001c0002t0005 others(1): Show |
14 | HG01884.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2601G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 2601 | chr22 | 39491550 | ||||||
| chr22:39491681 | A | G | 27 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(24): Show |
117 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*2732A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 2732 | chr22 | 39491681 | ||||||
| chr22:39491891 | G | T | 1 | a0001c0001t0014 | 2 | HG02895.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2942G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 2/2 | 2942 | chr22 | 39491891 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39457587 | C | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
10 | HG02280.hp2 HG02572.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2+30C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39457587 | |||||||
| chr22:39457700 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-2+143C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39457700 | |||||||
| chr22:39457735 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-2+178G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39457735 | |||||||
| chr22:39457736 | G | C | 32 | a0001c0001t0001g0036 a0001c0001t0001g0039 a0001c0001t0001g0048 others(29): Show |
38 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.-2+179G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39457736 | |||||||
| chr22:39458099 | AGGGCCCC others(19): Show |
A | 1 | a0001c0001t0004g0239 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-2+554_-2+579delCA others(24): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39458099 | ||||||
| chr22:39458350 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-2+793A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39458350 | |||||||
| chr22:39458362 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0029g0062 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-2+805G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39458362 | |||||||
| chr22:39458363 | C | G | 1 | a0001c0001t0001g0210 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-2+806C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39458363 | |||||||
| chr22:39458416 | C | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(215): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-2+859C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39458416 | |||||||
| chr22:39458545 | G | C | 8 | a0001c0001t0006g0031 a0001c0001t0006g0213 a0001c0001t0006g0214 others(5): Show |
9 | HG01175.hp1 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2+988G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39458545 | |||||||
| chr22:39458817 | A | G | 1 | a0001c0002t0016g0209 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-2+1260A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39458817 | |||||||
| chr22:39458979 | C | T | 2 | a0001c0001t0011g0030 a0001c0001t0027g0030 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+1422C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39458979 | |||||||
| chr22:39459072 | CT | C | 30 | a0001c0001t0001g0064 a0001c0001t0001g0241 a0001c0001t0001g0242 others(27): Show |
35 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-2+1534delT | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39459072 | ||||||
| chr22:39459072 | CTTTTTT | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(193): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.-2+1529_-2+1534del others(6): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39459072 | ||||||
| chr22:39459072 | CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0005g0200 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-2+1524_-2+1534del others(11): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39459072 | ||||||
| chr22:39459073 | T | TTTTCTTT others(2): Show |
9 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0208 others(6): Show |
11 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+1519_-2+1520ins others(9): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39459073 | ||||||
| chr22:39459073 | T | TTTTCTTT others(7): Show |
1 | a0001c0001t0001g0004 | 2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-2+1519_-2+1520ins others(14): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39459073 | ||||||
| chr22:39459073 | T | TTTTCTTT others(12): Show |
1 | a0001c0001t0001g0202 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-2+1519_-2+1520ins others(19): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39459073 | ||||||
| chr22:39459073 | T | TTTTCTTT others(17): Show |
1 | a0001c0002t0002g0204 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-2+1519_-2+1520ins others(24): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39459073 | ||||||
| chr22:39459078 | T | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(21): Show |
28 | HG00639.hp1 HG01243.hp2 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.-2+1521T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39459078 | |||||||
| chr22:39459083 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(217): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-2+1526T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39459083 | |||||||
| chr22:39459123 | G | C | 1 | a0001c0001t0019g0236 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-2+1566G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39459123 | |||||||
| chr22:39459185 | C | T | 3 | a0001c0001t0004g0219 a0001c0001t0004g0220 a0001c0001t0004g0239 |
3 | HG02129.hp1 NA18979.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-2+1628C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39459185 | |||||||
| chr22:39459489 | G | A | 1 | a0003c0009t0003g0067 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-2+1932G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39459489 | |||||||
| chr22:39459535 | G | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(219): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-2+1978G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39459535 | |||||||
| chr22:39459570 | C | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(195): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.-2+2013C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39459570 | |||||||
| chr22:39459723 | G | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(218): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-2+2166G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39459723 | |||||||
| chr22:39459878 | C | T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(218): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-2+2321C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39459878 | |||||||
| chr22:39460027 | A | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(134): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.-2+2470A>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39460027 | |||||||
| chr22:39460278 | G | T | 3 | a0001c0001t0004g0219 a0001c0001t0004g0220 a0001c0001t0004g0239 |
3 | HG02129.hp1 NA18979.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-2+2721G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39460278 | |||||||
| chr22:39460351 | G | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(218): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-2+2794G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39460351 | |||||||
| chr22:39460496 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-2+2939T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39460496 | |||||||
| chr22:39460510 | C | T | 8 | a0001c0001t0006g0031 a0001c0001t0006g0213 a0001c0001t0006g0214 others(5): Show |
9 | HG01175.hp1 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2+2953C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39460510 | |||||||
| chr22:39460650 | T | A | 1 | a0001c0001t0001g0210 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-2+3093T>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39460650 | |||||||
| chr22:39460976 | A | T | 2 | a0001c0003t0002g0198 a0001c0003t0002g0199 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-2+3419A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39460976 | |||||||
| chr22:39461042 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-2+3485C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39461042 | |||||||
| chr22:39461320 | G | C | 1 | a0001c0001t0019g0236 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-2+3763G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39461320 | |||||||
| chr22:39461413 | G | A | 2 | a0001c0003t0002g0198 a0001c0003t0002g0199 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-2+3856G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39461413 | |||||||
| chr22:39461635 | T | C | 2 | a0001c0001t0011g0030 a0001c0001t0027g0030 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+4078T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39461635 | |||||||
| chr22:39461721 | C | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0202 others(14): Show |
21 | HG00639.hp1 HG01243.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.-2+4164C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39461721 | |||||||
| chr22:39461885 | T | C | 5 | a0001c0001t0003g0070 a0001c0001t0010g0071 a0001c0002t0002g0068 others(2): Show |
5 | HG02280.hp1 HG02922.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+4328T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39461885 | |||||||
| chr22:39461904 | C | CT | 6 | a0001c0001t0004g0219 a0001c0001t0004g0220 a0001c0001t0004g0239 others(3): Show |
6 | HG02129.hp1 HG02257.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+4359dupT | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39461904 | ||||||
| chr22:39461904 | CT | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0072 others(17): Show |
24 | HG00639.hp1 HG01243.hp2 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.-2+4359delT | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39461904 | ||||||
| chr22:39461957 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-2+4400A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39461957 | |||||||
| chr22:39462012 | C | T | 2 | a0001c0002t0002g0117 a0001c0002t0005g0118 |
2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-2+4455C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39462012 | |||||||
| chr22:39462048 | C | T | 4 | a0001c0001t0004g0219 a0001c0001t0004g0220 a0001c0001t0004g0239 others(1): Show |
4 | HG02129.hp1 HG02257.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+4491C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39462048 | |||||||
| chr22:39462178 | C | T | 1 | a0001c0001t0004g0235 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-2+4621C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39462178 | |||||||
| chr22:39462191 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-2+4634A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39462191 | |||||||
| chr22:39462322 | C | T | 12 | a0001c0001t0004g0219 a0001c0001t0004g0220 a0001c0001t0004g0239 others(9): Show |
13 | HG01175.hp1 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-2+4765C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39462322 | |||||||
| chr22:39462412 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-2+4855A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39462412 | |||||||
| chr22:39463047 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0029g0062 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-2+5490G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39463047 | |||||||
| chr22:39463053 | A | T | 8 | a0001c0001t0006g0031 a0001c0001t0006g0213 a0001c0001t0006g0214 others(5): Show |
9 | HG01175.hp1 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2+5496A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39463053 | |||||||
| chr22:39463164 | C | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(226): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-2+5607C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39463164 | |||||||
| chr22:39463167 | A | G | 1 | a0001c0001t0001g0017 | 2 | HG01261.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-2+5610A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39463167 | |||||||
| chr22:39463231 | C | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-2+5674C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39463231 | |||||||
| chr22:39463518 | C | G | 18 | a0001c0001t0001g0063 a0001c0001t0001g0202 a0001c0001t0001g0203 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2+5961C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39463518 | |||||||
| chr22:39463538 | G | A | 18 | a0001c0001t0001g0063 a0001c0001t0001g0202 a0001c0001t0001g0203 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2+5981G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39463538 | |||||||
| chr22:39463584 | C | T | 1 | a0003c0009t0003g0067 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-2+6027C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39463584 | |||||||
| chr22:39463757 | A | T | 2 | a0001c0001t0003g0070 a0001c0001t0010g0071 |
2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-2+6200A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39463757 | |||||||
| chr22:39463921 | T | TA | 10 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0126 others(7): Show |
10 | HG02165.hp2 HG02602.hp1 HG03490.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+6373dupA | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39463921 | ||||||
| chr22:39463921 | TA | T | 18 | a0001c0001t0001g0063 a0001c0001t0001g0202 a0001c0001t0001g0203 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2+6373delA | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39463921 | ||||||
| chr22:39464125 | C | T | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(226): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-2+6568C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464125 | |||||||
| chr22:39464194 | G | C | 3 | a0001c0001t0004g0219 a0001c0001t0004g0220 a0001c0001t0004g0239 |
3 | HG02129.hp1 NA18979.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-2+6637G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464194 | |||||||
| chr22:39464196 | A | T | 3 | a0001c0001t0004g0219 a0001c0001t0004g0220 a0001c0001t0004g0239 |
3 | HG02129.hp1 NA18979.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-2+6639A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464196 | |||||||
| chr22:39464237 | G | A | 1 | a0001c0002t0002g0132 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-2+6680G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464237 | |||||||
| chr22:39464237 | G | T | 1 | a0001c0002t0018g0234 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-2+6680G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464237 | |||||||
| chr22:39464259 | C | T | 1 | a0001c0001t0019g0236 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-2+6702C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464259 | |||||||
| chr22:39464260 | C | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0243 a0001c0001t0008g0244 |
7 | HG02280.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+6703C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464260 | |||||||
| chr22:39464409 | C | A | 9 | a0001c0001t0006g0031 a0001c0001t0006g0213 a0001c0001t0006g0214 others(6): Show |
10 | HG01175.hp1 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+6852C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464409 | |||||||
| chr22:39464458 | G | T | 1 | a0001c0001t0020g0233 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-2+6901G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464458 | |||||||
| chr22:39464463 | G | A | 18 | a0001c0001t0001g0063 a0001c0001t0001g0202 a0001c0001t0001g0203 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2+6906G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464463 | |||||||
| chr22:39464488 | G | A | 1 | a0001c0001t0019g0236 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-2+6931G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464488 | |||||||
| chr22:39464584 | A | G | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(226): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-2+7027A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464584 | |||||||
| chr22:39464790 | GC | G | 4 | a0001c0001t0004g0219 a0001c0001t0004g0220 a0001c0001t0004g0239 others(1): Show |
4 | HG02129.hp1 HG02257.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+7236delC | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39464790 | ||||||
| chr22:39464851 | C | T | 1 | a0001c0001t0008g0201 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-2+7294C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464851 | |||||||
| chr22:39464863 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(224): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-2+7306A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464863 | |||||||
| chr22:39464902 | C | T | 2 | a0001c0001t0011g0065 a0001c0001t0011g0066 |
2 | HG00639.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-2+7345C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39464902 | |||||||
| chr22:39465172 | A | C | 2 | a0001c0001t0001g0194 a0001c0001t0028g0195 |
2 | HG01943.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-2+7615A>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39465172 | |||||||
| chr22:39465404 | C | G | 1 | a0001c0002t0002g0061 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-2+7847C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39465404 | |||||||
| chr22:39465515 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-2+7958C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39465515 | |||||||
| chr22:39465653 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-2+8096A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39465653 | |||||||
| chr22:39465697 | C | T | 13 | a0001c0001t0001g0063 a0001c0001t0001g0203 a0001c0001t0001g0208 others(10): Show |
13 | HG00639.hp1 HG01243.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.-2+8140C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39465697 | |||||||
| chr22:39465760 | C | T | 2 | a0001c0003t0002g0198 a0001c0003t0002g0199 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-2+8203C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39465760 | |||||||
| chr22:39465931 | TA | T | 9 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0001g0192 others(6): Show |
9 | HG00639.hp1 HG01516.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2+8391delA | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39465931 | ||||||
| chr22:39466033 | G | T | 1 | a0001c0001t0006g0217 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-2+8476G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466033 | |||||||
| chr22:39466062 | G | T | 1 | a0001c0001t0019g0236 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-2+8505G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466062 | |||||||
| chr22:39466183 | C | A | 1 | a0001c0001t0001g0133 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-2+8626C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466183 | |||||||
| chr22:39466200 | C | T | 1 | a0001c0002t0005g0200 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-2+8643C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466200 | |||||||
| chr22:39466336 | G | A | 199 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(196): Show |
237 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.-2+8779G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466336 | |||||||
| chr22:39466338 | T | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(97): Show |
130 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-2+8781T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466338 | |||||||
| chr22:39466384 | A | G | 1 | a0001c0001t0005g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-2+8827A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466384 | |||||||
| chr22:39466468 | G | A | 1 | a0001c0002t0002g0038 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-2+8911G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466468 | |||||||
| chr22:39466484 | C | T | 10 | a0001c0001t0001g0063 a0001c0001t0007g0075 a0001c0001t0008g0201 others(7): Show |
10 | HG02257.hp2 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+8927C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466484 | |||||||
| chr22:39466485 | C | G | 9 | a0001c0001t0001g0245 a0001c0001t0006g0216 a0001c0001t0008g0166 others(6): Show |
9 | HG00639.hp1 HG01934.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2+8928C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466485 | |||||||
| chr22:39466558 | C | A | 1 | a0001c0001t0001g0110 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-2+9001C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466558 | |||||||
| chr22:39466573 | C | T | 1 | a0001c0001t0039g0179 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-2+9016C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466573 | |||||||
| chr22:39466677 | G | C | 1 | a0001c0001t0004g0239 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-2+9120G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466677 | |||||||
| chr22:39466693 | G | T | 1 | a0001c0001t0008g0201 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-2+9136G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466693 | |||||||
| chr22:39466848 | T | C | 1 | a0001c0002t0002g0056 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-2+9291T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466848 | |||||||
| chr22:39466997 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0029g0062 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-2+9440T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39466997 | |||||||
| chr22:39467041 | C | T | 4 | a0001c0001t0003g0014 a0001c0001t0003g0080 a0001c0001t0003g0097 others(1): Show |
5 | HG00642.hp1 HG01255.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+9484C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467041 | |||||||
| chr22:39467080 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-2+9523A>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467080 | |||||||
| chr22:39467140 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-2+9583G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467140 | |||||||
| chr22:39467304 | G | T | 1 | a0001c0001t0004g0239 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-2+9747G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467304 | |||||||
| chr22:39467321 | G | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
124 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-2+9764G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467321 | |||||||
| chr22:39467332 | A | G | 1 | a0001c0002t0005g0238 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-2+9775A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467332 | |||||||
| chr22:39467346 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0029g0062 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-2+9789G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467346 | |||||||
| chr22:39467366 | G | A | 1 | a0001c0001t0032g0135 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-2+9809G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467366 | |||||||
| chr22:39467435 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-2+9878C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467435 | |||||||
| chr22:39467493 | A | G | 1 | a0001c0001t0001g0029 | 2 | HG03669.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-2+9936A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467493 | |||||||
| chr22:39467519 | GTGGGCAG others(6): Show |
G | 1 | a0001c0001t0006g0227 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-2+9965_-2+9977del others(13): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39467519 | ||||||
| chr22:39467640 | TTTTTC | T | 5 | a0001c0001t0001g0063 a0001c0001t0011g0030 a0001c0001t0027g0030 others(2): Show |
5 | HG02145.hp1 HG02976.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+10099_-2+10103d others(7): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39467640 | ||||||
| chr22:39467671 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-2+10114G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467671 | |||||||
| chr22:39467716 | T | TGTTTCGT others(3): Show |
11 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0082 others(8): Show |
14 | HG00738.hp1 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.-2+10168_-2+10169i others(12): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39467716 | ||||||
| chr22:39467722 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-2+10165G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467722 | |||||||
| chr22:39467726 | T | C | 24 | a0001c0001t0001g0005 a0001c0001t0001g0060 a0001c0001t0001g0074 others(21): Show |
28 | HG00642.hp1 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-2+10169T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467726 | |||||||
| chr22:39467733 | T | C | 1 | a0001c0002t0002g0056 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-2+10176T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467733 | |||||||
| chr22:39467739 | T | C | 6 | a0001c0002t0002g0038 a0001c0002t0002g0042 a0001c0002t0002g0043 others(3): Show |
6 | HG00597.hp1 HG00597.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+10182T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467739 | |||||||
| chr22:39467771 | G | A | 3 | a0001c0002t0002g0117 a0001c0002t0002g0204 a0001c0002t0002g0205 |
3 | HG01109.hp1 HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-2+10214G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467771 | |||||||
| chr22:39467809 | C | CA | 30 | a0001c0001t0001g0005 a0001c0001t0001g0060 a0001c0001t0001g0074 others(27): Show |
34 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.-2+10272dupA | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39467809 | ||||||
| chr22:39467809 | CA | C | 19 | a0001c0001t0001g0021 a0001c0001t0001g0096 a0001c0001t0001g0121 others(16): Show |
21 | HG01496.hp1 HG01515.hp1 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.-2+10272delA | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39467809 | ||||||
| chr22:39467828 | A | T | 1 | a0001c0001t0001g0036 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-2+10271A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467828 | |||||||
| chr22:39467845 | G | T | 1 | a0001c0001t0020g0233 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-2+10288G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467845 | |||||||
| chr22:39467975 | A | G | 3 | a0001c0001t0031g0163 a0001c0004t0009g0009 a0001c0004t0009g0164 |
5 | NA18952.hp2 NA18964.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+10418A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39467975 | |||||||
| chr22:39468124 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-2+10567C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39468124 | |||||||
| chr22:39468194 | G | A | 2 | a0001c0002t0005g0200 a0001c0005t0015g0011 |
3 | HG02559.hp1 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-2+10637G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39468194 | |||||||
| chr22:39468344 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0029g0062 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-2+10787C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39468344 | |||||||
| chr22:39468513 | A | T | 3 | a0001c0001t0005g0109 a0001c0001t0019g0236 a0001c0002t0016g0209 |
3 | HG01884.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-2+10956A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39468513 | |||||||
| chr22:39468638 | CAGGCCTG others(546): Show |
C | 3 | a0001c0001t0011g0030 a0001c0001t0027g0030 a0001c0002t0002g0056 |
3 | HG02145.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+11084_-2+11636d others(2): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39468638 | ||||||
| chr22:39468766 | C | T | 1 | a0003c0009t0003g0067 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-2+11209C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39468766 | |||||||
| chr22:39469009 | G | A | 1 | a0001c0001t0003g0028 | 2 | HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-2+11452G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39469009 | |||||||
| chr22:39469253 | T | C | 2 | a0001c0001t0004g0219 a0002c0006t0001g0140 |
2 | NA18979.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-2+11696T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39469253 | |||||||
| chr22:39469470 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
235 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-2+11913A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39469470 | |||||||
| chr22:39469505 | C | T | 3 | a0001c0001t0005g0109 a0001c0001t0019g0236 a0001c0002t0016g0209 |
3 | HG01884.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-2+11948C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39469505 | |||||||
| chr22:39469830 | G | A | 1 | a0003c0009t0003g0067 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-2+12273G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39469830 | |||||||
| chr22:39469919 | G | A | 1 | a0001c0002t0005g0200 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-2+12362G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39469919 | |||||||
| chr22:39470050 | G | T | 3 | a0001c0001t0005g0109 a0001c0001t0019g0236 a0001c0002t0016g0209 |
3 | HG01884.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-2+12493G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470050 | |||||||
| chr22:39470075 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(109): Show |
142 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.-2+12518T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470075 | |||||||
| chr22:39470161 | C | T | 3 | a0001c0001t0005g0109 a0001c0001t0019g0236 a0001c0002t0016g0209 |
3 | HG01884.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-2+12604C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470161 | |||||||
| chr22:39470162 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0193 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-2+12605G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470162 | |||||||
| chr22:39470170 | C | T | 1 | a0001c0001t0032g0135 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-2+12613C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470170 | |||||||
| chr22:39470171 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0029g0062 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-2+12614G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470171 | |||||||
| chr22:39470194 | TC | T | 3 | a0001c0001t0005g0109 a0001c0001t0019g0236 a0001c0002t0016g0209 |
3 | HG01884.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-2+12638delC | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470194 | |||||||
| chr22:39470324 | G | A | 3 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0004g0221 |
3 | HG02615.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-2+12767G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470324 | |||||||
| chr22:39470378 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0152 |
3 | HG03704.hp1 HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-2+12821A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470378 | |||||||
| chr22:39470451 | C | T | 1 | a0001c0001t0003g0130 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-2+12894C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470451 | |||||||
| chr22:39470466 | G | A | 2 | a0001c0001t0011g0065 a0001c0001t0011g0066 |
2 | HG00639.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-2+12909G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470466 | |||||||
| chr22:39470714 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0029g0062 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-2+13157C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470714 | |||||||
| chr22:39470789 | G | A | 5 | a0001c0001t0001g0072 a0001c0001t0001g0153 a0001c0001t0001g0165 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+13232G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470789 | |||||||
| chr22:39470933 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(107): Show |
140 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-2+13376T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39470933 | |||||||
| chr22:39471078 | G | A | 2 | a0001c0002t0005g0200 a0001c0005t0015g0011 |
3 | HG02559.hp1 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-2+13521G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39471078 | |||||||
| chr22:39471382 | C | T | 2 | a0001c0001t0006g0216 a0001c0001t0006g0218 |
2 | HG02717.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-2+13825C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39471382 | |||||||
| chr22:39471582 | C | T | 1 | a0001c0001t0010g0059 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-2+14025C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39471582 | |||||||
| chr22:39471599 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-2+14042C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39471599 | |||||||
| chr22:39471654 | C | T | 1 | a0001c0002t0016g0209 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-2+14097C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39471654 | |||||||
| chr22:39471656 | C | G | 88 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0074 others(85): Show |
99 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(96): Show |
intron_variant | MODIFIER | c.-2+14099C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39471656 | |||||||
| chr22:39471813 | A | G | 1 | a0001c0002t0018g0234 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-2+14256A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39471813 | |||||||
| chr22:39471964 | G | C | 3 | a0001c0001t0003g0102 a0001c0001t0008g0103 a0001c0001t0008g0244 |
3 | HG02886.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-2+14407G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39471964 | |||||||
| chr22:39472104 | G | C | 74 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0001g0074 others(71): Show |
82 | HG00140.hp2 HG00639.hp1 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.-2+14547G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472104 | |||||||
| chr22:39472120 | A | G | 10 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0035 others(7): Show |
13 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-2+14563A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472120 | |||||||
| chr22:39472155 | C | T | 1 | a0001c0002t0016g0209 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-2+14598C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472155 | |||||||
| chr22:39472178 | C | T | 1 | a0001c0002t0002g0068 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-2+14621C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472178 | |||||||
| chr22:39472254 | C | G | 1 | a0001c0001t0040g0113 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-2+14697C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472254 | |||||||
| chr22:39472296 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-2+14739T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472296 | |||||||
| chr22:39472339 | G | C | 1 | a0001c0001t0001g0126 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-2+14782G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472339 | |||||||
| chr22:39472369 | A | G | 1 | a0001c0002t0005g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-2+14812A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472369 | |||||||
| chr22:39472428 | A | G | 1 | a0001c0002t0016g0209 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-2+14871A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472428 | |||||||
| chr22:39472503 | A | G | 1 | a0001c0002t0016g0209 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-1-14844A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472503 | |||||||
| chr22:39472684 | G | A | 1 | a0001c0002t0016g0209 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-1-14663G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472684 | |||||||
| chr22:39472794 | G | A | 3 | a0001c0001t0031g0163 a0001c0004t0009g0009 a0001c0004t0009g0164 |
5 | NA18952.hp2 NA18964.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-14553G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472794 | |||||||
| chr22:39472862 | T | C | 1 | a0001c0001t0028g0195 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-1-14485T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472862 | |||||||
| chr22:39472870 | A | C | 1 | a0001c0001t0033g0182 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-1-14477A>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472870 | |||||||
| chr22:39472886 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0029g0062 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-1-14461G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39472886 | |||||||
| chr22:39473204 | C | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(177): Show |
218 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.-1-14143C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39473204 | |||||||
| chr22:39473577 | A | G | 3 | a0001c0001t0031g0163 a0001c0004t0009g0009 a0001c0004t0009g0164 |
5 | NA18952.hp2 NA18964.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-13770A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39473577 | |||||||
| chr22:39473578 | T | G | 1 | a0001c0002t0016g0209 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-1-13769T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39473578 | |||||||
| chr22:39473714 | A | G | 54 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0001g0074 others(51): Show |
60 | HG00140.hp2 HG01109.hp1 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.-1-13633A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39473714 | |||||||
| chr22:39473774 | C | T | 1 | a0001c0001t0004g0232 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-1-13573C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39473774 | |||||||
| chr22:39473992 | T | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(177): Show |
219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.-1-13355T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39473992 | |||||||
| chr22:39474294 | G | T | 2 | a0001c0001t0005g0109 a0001c0001t0019g0236 |
2 | HG01884.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-1-13053G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474294 | |||||||
| chr22:39474304 | A | G | 1 | a0001c0001t0005g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-1-13043A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474304 | |||||||
| chr22:39474553 | A | G | 2 | a0001c0001t0014g0076 a0001c0001t0014g0078 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-1-12794A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474553 | |||||||
| chr22:39474655 | C | G | 3 | a0001c0001t0003g0102 a0001c0001t0008g0103 a0001c0001t0008g0244 |
3 | HG02886.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-1-12692C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474655 | |||||||
| chr22:39474662 | C | T | 1 | a0001c0002t0005g0106 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-1-12685C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474662 | |||||||
| chr22:39474795 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-1-12552G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474795 | |||||||
| chr22:39474814 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0111 a0001c0001t0001g0112 others(2): Show |
8 | HG00735.hp1 HG01255.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-12533G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474814 | |||||||
| chr22:39474909 | G | A | 1 | a0001c0001t0001g0019 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-1-12438G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474909 | |||||||
| chr22:39474970 | G | A | 1 | a0001c0002t0005g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-1-12377G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474970 | |||||||
| chr22:39474982 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-1-12365C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474982 | |||||||
| chr22:39474998 | C | T | 2 | a0001c0001t0003g0157 a0001c0001t0003g0158 |
2 | HG01952.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-1-12349C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39474998 | |||||||
| chr22:39475052 | A | G | 3 | a0001c0001t0031g0163 a0001c0004t0009g0009 a0001c0004t0009g0164 |
5 | NA18952.hp2 NA18964.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-12295A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475052 | |||||||
| chr22:39475074 | C | T | 1 | a0001c0001t0007g0049 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-1-12273C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475074 | |||||||
| chr22:39475122 | G | C | 3 | a0001c0001t0003g0102 a0001c0001t0008g0103 a0001c0001t0008g0244 |
3 | HG02886.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-1-12225G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475122 | |||||||
| chr22:39475123 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-1-12224C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475123 | |||||||
| chr22:39475128 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0072 a0001c0001t0001g0153 |
2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-1-12206_-1-12197d others(12): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | ||||||
| chr22:39475128 | C | CTTTTTTT others(9): Show |
4 | a0001c0001t0001g0077 a0001c0001t0001g0202 a0001c0001t0001g0203 others(1): Show |
4 | HG02809.hp1 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-12212_-1-12197d others(18): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | ||||||
| chr22:39475128 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0004 a0001c0001t0001g0165 |
6 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-12213_-1-12197d others(19): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | ||||||
| chr22:39475128 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0001g0245 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-1-12217_-1-12197d others(23): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | ||||||
| chr22:39475128 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0038g0050 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-1-12197_-1-12196i others(26): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | ||||||
| chr22:39475128 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0001g0096 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-1-12197_-1-12196i others(27): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | ||||||
| chr22:39475128 | C | CTTTTTTT others(25): Show |
1 | a0001c0001t0001g0242 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-1-12197_-1-12196i others(34): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | ||||||
| chr22:39475128 | C | CTTTTTTT others(26): Show |
1 | a0001c0001t0001g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-1-12197_-1-12196i others(35): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | ||||||
| chr22:39475128 | CT | C | 42 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0060 others(39): Show |
51 | HG00642.hp1 HG00738.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-1-12197delT | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | ||||||
| chr22:39475128 | CTT | C | 9 | a0001c0001t0001g0063 a0001c0001t0001g0081 a0001c0001t0001g0156 others(6): Show |
11 | HG01081.hp2 HG01106.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-12198_-1-12197d others(4): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | ||||||
| chr22:39475128 | CTTT | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(77): Show |
106 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.-1-12199_-1-12197d others(5): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | ||||||
| chr22:39475128 | CTTTT | C | 6 | a0001c0001t0005g0109 a0001c0001t0011g0065 a0001c0001t0011g0066 others(3): Show |
6 | HG00639.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-12200_-1-12197d others(6): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39475128 | ||||||
| chr22:39475490 | G | A | 1 | a0001c0002t0005g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-1-11857G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475490 | |||||||
| chr22:39475561 | C | T | 1 | a0001c0001t0032g0135 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-1-11786C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475561 | |||||||
| chr22:39475574 | T | G | 1 | a0001c0001t0006g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-1-11773T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475574 | |||||||
| chr22:39475616 | G | A | 1 | a0001c0002t0005g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-1-11731G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475616 | |||||||
| chr22:39475723 | A | G | 11 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0160 others(8): Show |
11 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-11624A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475723 | |||||||
| chr22:39475784 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-1-11563C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475784 | |||||||
| chr22:39475938 | C | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0082 others(8): Show |
14 | HG00738.hp1 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-11409C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39475938 | |||||||
| chr22:39476009 | C | T | 1 | a0001c0001t0008g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-1-11338C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476009 | |||||||
| chr22:39476068 | A | G | 69 | a0001c0001t0001g0022 a0001c0001t0001g0054 a0001c0001t0001g0055 others(66): Show |
74 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-1-11279A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476068 | |||||||
| chr22:39476122 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.-1-11225A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476122 | |||||||
| chr22:39476174 | A | C | 2 | a0001c0001t0014g0076 a0001c0001t0014g0078 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-1-11173A>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476174 | |||||||
| chr22:39476211 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-1-11136G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476211 | |||||||
| chr22:39476302 | A | G | 9 | a0001c0001t0003g0102 a0001c0001t0005g0109 a0001c0001t0008g0103 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1-11045A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476302 | |||||||
| chr22:39476411 | G | A | 3 | a0001c0001t0011g0030 a0001c0001t0027g0030 a0001c0002t0002g0056 |
3 | HG02145.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-1-10936G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476411 | |||||||
| chr22:39476649 | G | A | 6 | a0001c0001t0002g0046 a0001c0001t0007g0007 a0001c0001t0007g0047 others(3): Show |
8 | HG01175.hp1 HG02109.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-10698G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476649 | |||||||
| chr22:39476674 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-1-10673C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476674 | |||||||
| chr22:39476695 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0019 others(61): Show |
86 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.-1-10652C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476695 | |||||||
| chr22:39476702 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(170): Show |
212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.-1-10645G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476702 | |||||||
| chr22:39476800 | C | T | 10 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0035 others(7): Show |
13 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1-10547C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476800 | |||||||
| chr22:39476851 | C | CACTTTGT others(13): Show |
1 | a0001c0001t0006g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-10495_-1-10476d others(22): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39476851 | ||||||
| chr22:39476939 | T | C | 1 | a0001c0001t0004g0224 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-1-10408T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39476939 | |||||||
| chr22:39477053 | A | G | 4 | a0001c0001t0011g0065 a0001c0001t0011g0066 a0001c0001t0014g0076 others(1): Show |
4 | HG00639.hp1 HG01934.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-10294A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477053 | |||||||
| chr22:39477318 | C | T | 4 | a0001c0001t0003g0102 a0001c0001t0008g0103 a0001c0001t0008g0201 others(1): Show |
4 | HG02257.hp2 HG02258.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-10029C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477318 | |||||||
| chr22:39477465 | A | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(186): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.-1-9882A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477465 | |||||||
| chr22:39477552 | G | GA | 7 | a0001c0001t0001g0082 a0001c0001t0001g0134 a0001c0001t0003g0157 others(4): Show |
7 | HG00639.hp1 HG01361.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-9781dupA | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39477552 | ||||||
| chr22:39477552 | GA | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(84): Show |
115 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-1-9781delA | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39477552 | ||||||
| chr22:39477567 | C | A | 2 | a0001c0001t0006g0217 a0001c0001t0022g0215 |
2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-1-9780C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477567 | |||||||
| chr22:39477624 | C | T | 4 | a0001c0001t0011g0065 a0001c0001t0011g0066 a0001c0001t0014g0076 others(1): Show |
4 | HG00639.hp1 HG01934.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-9723C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477624 | |||||||
| chr22:39477801 | C | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0001g0077 others(6): Show |
13 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-1-9546C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477801 | |||||||
| chr22:39477864 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-1-9483C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477864 | |||||||
| chr22:39477910 | G | A | 3 | a0001c0001t0011g0030 a0001c0001t0027g0030 a0001c0002t0002g0056 |
3 | HG02145.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-1-9437G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477910 | |||||||
| chr22:39477914 | C | A | 1 | a0001c0002t0002g0206 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-1-9433C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477914 | |||||||
| chr22:39477924 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0181 a0001c0001t0004g0224 |
4 | HG00323.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-9423G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477924 | |||||||
| chr22:39477932 | G | A | 26 | a0001c0001t0001g0010 a0001c0001t0001g0114 a0001c0001t0001g0122 others(23): Show |
33 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-1-9415G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39477932 | |||||||
| chr22:39478151 | G | A | 2 | a0001c0001t0004g0226 a0001c0002t0005g0118 |
2 | HG01433.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-1-9196G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39478151 | |||||||
| chr22:39478153 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-1-9194G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39478153 | |||||||
| chr22:39478309 | A | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(213): Show |
263 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.-1-9038A>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39478309 | |||||||
| chr22:39478315 | A | G | 1 | a0001c0002t0002g0068 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-1-9032A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39478315 | |||||||
| chr22:39478361 | A | G | 5 | a0001c0001t0003g0102 a0001c0001t0008g0103 a0001c0001t0008g0201 others(2): Show |
5 | HG02257.hp2 HG02258.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-8986A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39478361 | |||||||
| chr22:39478566 | G | C | 8 | a0001c0001t0001g0063 a0001c0001t0001g0096 a0001c0001t0001g0241 others(5): Show |
8 | HG02965.hp2 HG02976.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-8781G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39478566 | |||||||
| chr22:39478785 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0017 others(133): Show |
163 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.-1-8562A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39478785 | |||||||
| chr22:39478832 | C | T | 1 | a0001c0001t0004g0226 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-1-8515C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39478832 | |||||||
| chr22:39478917 | C | T | 1 | a0001c0001t0004g0221 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-1-8430C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39478917 | |||||||
| chr22:39479135 | C | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG00738.hp1 HG01074.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-1-8212C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479135 | |||||||
| chr22:39479195 | GCCGAGTG others(10): Show |
G | 2 | a0001c0001t0001g0129 a0001c0001t0003g0159 |
2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-1-8149_-1-8133del others(17): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39479195 | ||||||
| chr22:39479213 | C | T | 1 | a0001c0002t0005g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-1-8134C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479213 | |||||||
| chr22:39479310 | G | T | 1 | a0001c0005t0015g0011 | 2 | NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-1-8037G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479310 | |||||||
| chr22:39479442 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-1-7905T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479442 | |||||||
| chr22:39479459 | G | A | 1 | a0001c0001t0004g0229 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-1-7888G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479459 | |||||||
| chr22:39479532 | C | T | 1 | a0001c0002t0002g0044 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-1-7815C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479532 | |||||||
| chr22:39479590 | G | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.-1-7757G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479590 | |||||||
| chr22:39479620 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0038g0050 |
2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-1-7727C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479620 | |||||||
| chr22:39479662 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-1-7685T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479662 | |||||||
| chr22:39479785 | C | G | 1 | a0001c0001t0030g0186 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-1-7562C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479785 | |||||||
| chr22:39479790 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-1-7557C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479790 | |||||||
| chr22:39479835 | C | T | 1 | a0001c0001t0008g0201 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-1-7512C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479835 | |||||||
| chr22:39479848 | T | C | 1 | a0001c0005t0015g0011 | 2 | NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-1-7499T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479848 | |||||||
| chr22:39479856 | C | T | 1 | a0001c0002t0016g0209 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-1-7491C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479856 | |||||||
| chr22:39479910 | C | T | 3 | a0001c0001t0031g0163 a0001c0004t0009g0009 a0001c0004t0009g0164 |
5 | NA18952.hp2 NA18964.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-7437C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479910 | |||||||
| chr22:39479961 | T | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(177): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.-1-7386T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39479961 | |||||||
| chr22:39480099 | C | T | 3 | a0001c0001t0031g0163 a0001c0004t0009g0009 a0001c0004t0009g0164 |
5 | NA18952.hp2 NA18964.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-7248C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39480099 | |||||||
| chr22:39480316 | C | T | 2 | a0001c0002t0002g0104 a0001c0002t0002g0108 |
2 | NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-1-7031C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39480316 | |||||||
| chr22:39480336 | C | T | 10 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0035 others(7): Show |
13 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1-7011C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39480336 | |||||||
| chr22:39480361 | C | A | 1 | a0001c0002t0005g0238 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-1-6986C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39480361 | |||||||
| chr22:39480366 | G | A | 2 | a0001c0001t0014g0076 a0001c0001t0014g0078 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-1-6981G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39480366 | |||||||
| chr22:39480579 | C | T | 2 | a0001c0001t0008g0201 a0003c0009t0003g0067 |
2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-1-6768C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39480579 | |||||||
| chr22:39480768 | G | T | 3 | a0001c0001t0001g0048 a0001c0001t0005g0109 a0001c0001t0019g0236 |
3 | HG01884.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-1-6579G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39480768 | |||||||
| chr22:39480833 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0004g0032 |
4 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-6514A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39480833 | |||||||
| chr22:39481082 | G | T | 31 | a0001c0001t0001g0048 a0001c0001t0001g0072 a0001c0001t0001g0074 others(28): Show |
34 | HG01167.hp1 HG01175.hp1 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.-1-6265G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481082 | |||||||
| chr22:39481336 | C | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0086 a0001c0001t0001g0087 others(4): Show |
10 | HG00735.hp1 HG00738.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-6011C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481336 | |||||||
| chr22:39481337 | G | A | 18 | a0001c0001t0001g0060 a0001c0001t0001g0156 a0001c0001t0001g0165 others(15): Show |
22 | HG01109.hp2 HG01175.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-1-6010G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481337 | |||||||
| chr22:39481391 | G | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0086 a0001c0001t0001g0087 others(5): Show |
11 | HG00735.hp1 HG00738.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-5956G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481391 | |||||||
| chr22:39481479 | C | T | 1 | a0001c0002t0005g0105 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-1-5868C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481479 | |||||||
| chr22:39481551 | G | T | 8 | a0001c0002t0002g0068 a0001c0002t0002g0069 a0001c0002t0002g0104 others(5): Show |
8 | HG01167.hp1 HG03490.hp2 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-5796G>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481551 | |||||||
| chr22:39481642 | G | A | 6 | a0001c0001t0007g0007 a0001c0001t0007g0047 a0001c0001t0007g0049 others(3): Show |
8 | HG01175.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-5705G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481642 | |||||||
| chr22:39481808 | C | T | 1 | a0001c0001t0008g0166 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-1-5539C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481808 | |||||||
| chr22:39481809 | T | C | 12 | a0001c0001t0005g0109 a0001c0001t0019g0236 a0001c0002t0005g0015 others(9): Show |
14 | HG01884.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-5538T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481809 | |||||||
| chr22:39481816 | G | A | 1 | a0001c0001t0023g0168 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-1-5531G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481816 | |||||||
| chr22:39481844 | G | A | 7 | a0001c0001t0007g0007 a0001c0001t0007g0047 a0001c0001t0007g0049 others(4): Show |
9 | HG00609.hp2 HG01175.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1-5503G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39481844 | |||||||
| chr22:39482147 | A | AT | 93 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0019 others(90): Show |
121 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.-1-5180dupT | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39482147 | ||||||
| chr22:39482147 | AT | A | 11 | a0001c0001t0008g0103 a0001c0001t0008g0201 a0001c0001t0008g0244 others(8): Show |
11 | HG00639.hp1 HG01934.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1-5180delT | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39482147 | ||||||
| chr22:39482147 | ATTTTTT | A | 24 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0028 others(21): Show |
28 | HG00140.hp2 HG00642.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1-5185_-1-5180del others(6): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39482147 | ||||||
| chr22:39482559 | C | G | 1 | a0003c0009t0003g0067 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-1-4788C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39482559 | |||||||
| chr22:39482692 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-1-4655G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39482692 | |||||||
| chr22:39482936 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-1-4411G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39482936 | |||||||
| chr22:39482948 | C | T | 1 | a0001c0002t0018g0234 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-1-4399C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39482948 | |||||||
| chr22:39482951 | G | C | 1 | a0001c0001t0023g0168 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-1-4396G>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39482951 | |||||||
| chr22:39482993 | T | C | 62 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0048 others(59): Show |
70 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.-1-4354T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39482993 | |||||||
| chr22:39483035 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-1-4312C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483035 | |||||||
| chr22:39483057 | T | C | 1 | a0001c0001t0008g0166 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-1-4290T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483057 | |||||||
| chr22:39483297 | C | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | HG00741.hp1 HG01361.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-4050C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483297 | |||||||
| chr22:39483415 | G | A | 3 | a0001c0001t0008g0103 a0001c0001t0008g0201 a0001c0001t0008g0244 |
3 | HG02257.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-1-3932G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483415 | |||||||
| chr22:39483439 | C | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0077 a0001c0001t0001g0165 others(3): Show |
10 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-3908C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483439 | |||||||
| chr22:39483467 | A | G | 2 | a0001c0002t0002g0069 a0001c0002t0002g0120 |
2 | NA18963.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-1-3880A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483467 | |||||||
| chr22:39483501 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-1-3846T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483501 | |||||||
| chr22:39483502 | TA | T | 100 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0048 others(97): Show |
113 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.-1-3834delA | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39483502 | ||||||
| chr22:39483626 | C | T | 1 | a0001c0001t0008g0166 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-1-3721C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483626 | |||||||
| chr22:39483644 | C | G | 3 | a0001c0001t0008g0103 a0001c0001t0008g0201 a0001c0001t0008g0244 |
3 | HG02257.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-1-3703C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483644 | |||||||
| chr22:39483674 | A | T | 106 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0048 others(103): Show |
121 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.-1-3673A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483674 | |||||||
| chr22:39483946 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-1-3401C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483946 | |||||||
| chr22:39483960 | G | A | 2 | a0001c0001t0006g0217 a0001c0001t0022g0215 |
2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-1-3387G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39483960 | |||||||
| chr22:39484021 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-1-3326C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39484021 | |||||||
| chr22:39484148 | A | T | 1 | a0001c0001t0008g0166 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-1-3199A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39484148 | |||||||
| chr22:39484163 | A | G | 5 | a0001c0001t0011g0030 a0001c0001t0011g0065 a0001c0001t0011g0066 others(2): Show |
5 | HG00639.hp1 HG01934.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-3184A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39484163 | |||||||
| chr22:39484361 | T | G | 1 | a0001c0001t0001g0143 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-1-2986T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39484361 | |||||||
| chr22:39484365 | T | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0180 |
2 | HG02080.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-1-2982T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39484365 | |||||||
| chr22:39484438 | T | A | 1 | a0001c0001t0004g0219 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-1-2909T>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39484438 | |||||||
| chr22:39484536 | C | G | 3 | a0001c0001t0011g0030 a0001c0001t0027g0030 a0001c0002t0002g0056 |
3 | HG02145.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-1-2811C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39484536 | |||||||
| chr22:39484995 | C | T | 118 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0073 others(115): Show |
136 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.-1-2352C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39484995 | |||||||
| chr22:39485135 | T | G | 28 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0014 others(25): Show |
33 | HG00140.hp2 HG00642.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.-1-2212T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485135 | |||||||
| chr22:39485256 | A | G | 2 | a0001c0004t0009g0009 a0001c0004t0009g0164 |
4 | NA18964.hp2 NA19007.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-2091A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485256 | |||||||
| chr22:39485285 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-1-2062G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485285 | |||||||
| chr22:39485565 | C | G | 1 | a0001c0001t0006g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1782C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485565 | |||||||
| chr22:39485566 | G | A | 1 | a0001c0001t0006g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1781G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485566 | |||||||
| chr22:39485587 | T | G | 1 | a0001c0001t0006g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1760T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485587 | |||||||
| chr22:39485588 | C | G | 5 | a0001c0001t0011g0030 a0001c0001t0011g0065 a0001c0001t0011g0066 others(2): Show |
5 | HG00639.hp1 HG01934.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-1759C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485588 | |||||||
| chr22:39485588 | C | T | 1 | a0001c0001t0006g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1759C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485588 | |||||||
| chr22:39485590 | A | G | 1 | a0001c0001t0006g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1757A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485590 | |||||||
| chr22:39485592 | A | G | 1 | a0001c0001t0006g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1755A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485592 | |||||||
| chr22:39485593 | C | T | 1 | a0001c0001t0006g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1754C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485593 | |||||||
| chr22:39485594 | C | G | 1 | a0001c0001t0006g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1753C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485594 | |||||||
| chr22:39485598 | C | G | 1 | a0001c0001t0006g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1749C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485598 | |||||||
| chr22:39485600 | A | G | 1 | a0001c0001t0006g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1747A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485600 | |||||||
| chr22:39485607 | A | G | 1 | a0001c0001t0006g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1740A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485607 | |||||||
| chr22:39485611 | C | G | 1 | a0001c0001t0006g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1736C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485611 | |||||||
| chr22:39485612 | GAAACCCC others(23): Show |
G | 1 | a0001c0001t0006g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1734_-1-1705del others(30): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485612 | |||||||
| chr22:39485643 | T | G | 1 | a0001c0001t0006g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1704T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485643 | |||||||
| chr22:39485644 | A | G | 1 | a0001c0001t0006g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1703A>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485644 | |||||||
| chr22:39485646 | C | G | 1 | a0001c0001t0006g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1701C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485646 | |||||||
| chr22:39485651 | T | A | 1 | a0001c0001t0006g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1696T>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485651 | |||||||
| chr22:39485654 | G | GGGAATGA others(3): Show |
1 | a0001c0001t0006g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-1692_-1-1691ins others(10): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39485654 | ||||||
| chr22:39485744 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-1-1603G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485744 | |||||||
| chr22:39485816 | C | A | 1 | a0001c0001t0008g0103 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-1-1531C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485816 | |||||||
| chr22:39485833 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-1-1514G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485833 | |||||||
| chr22:39485881 | T | G | 3 | a0001c0001t0008g0103 a0001c0001t0008g0201 a0001c0001t0008g0244 |
3 | HG02257.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-1-1466T>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485881 | |||||||
| chr22:39485895 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-1-1452G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485895 | |||||||
| chr22:39485951 | C | A | 1 | a0001c0001t0001g0185 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-1-1396C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485951 | |||||||
| chr22:39485953 | C | G | 1 | a0001c0003t0002g0161 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-1-1394C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39485953 | |||||||
| chr22:39486007 | G | A | 1 | a0001c0001t0012g0228 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1-1340G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39486007 | |||||||
| chr22:39486144 | AT | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
203 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.-1-1184delT | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39486144 | ||||||
| chr22:39486144 | ATT | A | 65 | a0001c0001t0001g0083 a0001c0001t0001g0141 a0001c0001t0001g0143 others(62): Show |
77 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.-1-1185_-1-1184del others(2): Show |
MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr22 | 39486144 | ||||||
| chr22:39486163 | T | A | 1 | a0001c0001t0002g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-1-1184T>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39486163 | |||||||
| chr22:39486179 | C | G | 2 | a0001c0001t0014g0076 a0001c0001t0014g0078 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-1-1168C>G | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39486179 | |||||||
| chr22:39486554 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-1-793G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39486554 | |||||||
| chr22:39486582 | C | T | 1 | a0001c0001t0029g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-1-765C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39486582 | |||||||
| chr22:39486781 | G | A | 1 | a0001c0001t0029g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-1-566G>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39486781 | |||||||
| chr22:39486792 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-1-555C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39486792 | |||||||
| chr22:39486811 | C | A | 6 | a0001c0001t0007g0007 a0001c0001t0007g0047 a0001c0001t0007g0049 others(3): Show |
8 | HG01175.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-536C>A | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39486811 | |||||||
| chr22:39486949 | A | T | 1 | a0001c0001t0003g0145 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-1-398A>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39486949 | |||||||
| chr22:39487053 | C | T | 3 | a0001c0002t0002g0008 a0001c0002t0002g0034 a0001c0002t0002g0154 |
5 | HG00597.hp2 HG00609.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-294C>T | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39487053 | |||||||
| chr22:39487246 | AC | A | 3 | a0001c0001t0008g0103 a0001c0001t0008g0201 a0001c0001t0008g0244 |
3 | HG02257.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-1-100delC | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39487246 | |||||||
| chr22:39487339 | T | C | 53 | a0001c0001t0005g0109 a0001c0001t0012g0225 a0001c0001t0012g0228 others(50): Show |
60 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(57): Show |
splice_region_variant&intron_variant | LOW | c.-1-8T>C | MGAT3 | ENSG00000128268.12 | transcript | ENST00000341184.7 | protein_coding | 1/1 | chr22 | 39487339 |