Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 83592 |
| ensemblid | ENSG00000165568.18 |
| hgncid | 23437 |
| symbol | AKR1E2 |
| name | aldo-keto reductase family 1 member E2 |
| refseq_nuc | NM_001040177.3 |
| refseq_prot | NP_001035267.1 |
| ensembl_nuc | ENST00000298375.12 |
| ensembl_prot | ENSP00000298375.7 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 4826207 |
| end | 4848062 |
| strand | + |
| ver | v1.2 |
| region | chr10:4826207-4848062 |
| region5000 | chr10:4821207-4853062 |
| regionname0 | AKR1E2_chr10_4826207_4848062 |
| regionname5000 | AKR1E2_chr10_4821207_4853062 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 320 | 296 | 78 | 58 | 114 | 10 | 34 | 76 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | MGDIP others(315): Show |
chr10 | 4821207 | 4853062 |
| a0002 | 0/0 | 320 | 29 | 1 | 3 | 25 | 0 | 0 | 21 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | MGDIP others(315): Show |
chr10 | 4821207 | 4853062 |
| a0003 | 0/0 | 320 | 11 | 3 | 8 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | MGDIP others(315): Show |
chr10 | 4821207 | 4853062 |
| a0004 | 0/0 | 300 | 11 | 2 | 5 | 0 | 0 | 4 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | MGDIP others(295): Show |
chr10 | 4821207 | 4853062 |
| a0005 | 0/0 | 320 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | MGDIP others(315): Show |
chr10 | 4821207 | 4853062 |
| a0006 | 0/0 | 320 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | MGDIP others(315): Show |
chr10 | 4821207 | 4853062 |
| a0007 | 0/0 | 320 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | MGDIP others(315): Show |
chr10 | 4821207 | 4853062 |
| a0008 | 0/0 | 320 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | MGDIP others(315): Show |
chr10 | 4821207 | 4853062 |
| a0009 | 0/0 | 320 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | MGDIP others(315): Show |
chr10 | 4821207 | 4853062 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 960 | 294 | 77 | 57 | 114 | 10 | 34 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | ATGGG others(955): Show |
chr10 | 4821207 | 4853062 | ||
| a0001c0009 | 0/0 | 960 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | ATGGG others(955): Show |
chr10 | 4821207 | 4853062 | ||
| a0001c0011 | 0/0 | 960 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | ATGGG others(955): Show |
chr10 | 4821207 | 4853062 | ||
| a0002c0002 | 0/0 | 960 | 29 | 1 | 3 | 25 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | ATGGG others(955): Show |
chr10 | 4821207 | 4853062 | ||
| a0003c0003 | 0/0 | 960 | 11 | 3 | 8 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | ATGGG others(955): Show |
chr10 | 4821207 | 4853062 | ||
| a0004c0004 | 0/0 | 960 | 11 | 2 | 5 | 0 | 0 | 4 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | ATGGG others(955): Show |
chr10 | 4821207 | 4853062 | ||
| a0005c0005 | 0/0 | 960 | 4 | 4 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | ATGGG others(955): Show |
chr10 | 4821207 | 4853062 | ||
| a0006c0006 | 0/0 | 960 | 3 | 0 | 0 | 3 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | ATGGG others(955): Show |
chr10 | 4821207 | 4853062 | ||
| a0007c0007 | 0/0 | 960 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | ATGGG others(955): Show |
chr10 | 4821207 | 4853062 | ||
| a0008c0008 | 0/0 | 960 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | ATGGG others(955): Show |
chr10 | 4821207 | 4853062 | ||
| a0009c0010 | 0/0 | 960 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | ATGGG others(955): Show |
chr10 | 4821207 | 4853062 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1613 | 224 | 32 | 49 | 109 | 10 | 23 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1608): Show |
chr10 | 4821207 | 4853062 |
| a0001c0001t0002 | 1/0 | 1613 | 58 | 39 | 6 | 2 | 0 | 10 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1608): Show |
chr10 | 4821207 | 4853062 |
| a0001c0001t0004 | 0/0 | 1613 | 2 | 1 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1608): Show |
chr10 | 4821207 | 4853062 |
| a0001c0001t0008 | 0/0 | 1613 | 3 | 0 | 0 | 3 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1608): Show |
chr10 | 4821207 | 4853062 |
| a0001c0001t0009 | 0/0 | 1613 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1608): Show |
chr10 | 4821207 | 4853062 |
| a0001c0001t0010 | 0/0 | 1621 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1616): Show |
chr10 | 4821207 | 4853062 |
| a0001c0001t0011 | 0/0 | 1613 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1608): Show |
chr10 | 4821207 | 4853062 |
| a0001c0001t0013 | 0/0 | 1613 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1608): Show |
chr10 | 4821207 | 4853062 |
| a0001c0001t0015 | 0/0 | 1613 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1608): Show |
chr10 | 4821207 | 4853062 |
| a0001c0009t0002 | 0/0 | 1613 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1608): Show |
chr10 | 4821207 | 4853062 |
| a0001c0011t0001 | 0/0 | 1613 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1608): Show |
chr10 | 4821207 | 4853062 |
| a0002c0002t0003 | 0/0 | 1614 | 27 | 1 | 3 | 23 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1609): Show |
chr10 | 4821207 | 4853062 |
| a0002c0002t0012 | 0/0 | 1622 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1617): Show |
chr10 | 4821207 | 4853062 |
| a0002c0002t0014 | 0/0 | 1614 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1609): Show |
chr10 | 4821207 | 4853062 |
| a0003c0003t0004 | 0/0 | 1613 | 11 | 3 | 8 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1608): Show |
chr10 | 4821207 | 4853062 |
| a0004c0004t0005 | 0/0 | 1613 | 8 | 2 | 3 | 0 | 0 | 3 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1608): Show |
chr10 | 4821207 | 4853062 |
| a0004c0004t0007 | 0/0 | 1613 | 3 | 0 | 2 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1608): Show |
chr10 | 4821207 | 4853062 |
| a0005c0005t0006 | 0/0 | 1605 | 4 | 4 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1600): Show |
chr10 | 4821207 | 4853062 |
| a0006c0006t0001 | 0/0 | 1613 | 3 | 0 | 0 | 3 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1608): Show |
chr10 | 4821207 | 4853062 |
| a0007c0007t0002 | 0/0 | 1613 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1608): Show |
chr10 | 4821207 | 4853062 |
| a0008c0008t0001 | 0/0 | 1613 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1608): Show |
chr10 | 4821207 | 4853062 |
| a0009c0010t0001 | 0/0 | 1613 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | GTCAC others(1608): Show |
chr10 | 4821207 | 4853062 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 50 | 1 | 17 | 26 | 0 | 6 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0002 | 0/0 | 34 | 1 | 6 | 20 | 2 | 5 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0004 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0005 | 0/0 | 10 | 2 | 3 | 3 | 0 | 2 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0006 | 0/0 | 10 | 0 | 6 | 0 | 2 | 2 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0007 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0012 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0017 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0002 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0003 | 0/0 | 16 | 11 | 0 | 0 | 0 | 5 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0019 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0021 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0004g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0008g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0008g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0009g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0010g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0011g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0013g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0015g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0009t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0011t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0012g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0014g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0003c0003t0004g0010 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0003c0003t0004g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0003c0003t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0003c0003t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0003c0003t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0004c0004t0005g0023 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0004c0004t0005g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0004c0004t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0004c0004t0005g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0004c0004t0005g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0004c0004t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0004c0004t0007g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0004c0004t0007g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0004c0004t0007g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0005c0005t0006g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0005c0005t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0006c0006t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0007c0007t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0008c0008t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0009c0010t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | GBR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00642 | hp1 | a0002 | c0002 | t0003 | g0048 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00642 | hp2 | a0001 | c0011 | t0001 | g0001 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00735 | hp1 | a0003 | c0003 | t0004 | g0010 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00741 | hp1 | a0003 | c0003 | t0004 | g0010 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00741 | hp2 | a0002 | c0002 | t0003 | g0024 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01070 | hp2 | a0003 | c0003 | t0004 | g0010 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01071 | hp2 | a0003 | c0003 | t0004 | g0010 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01074 | hp2 | a0003 | c0003 | t0004 | g0010 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0037 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01106 | hp2 | a0002 | c0002 | t0003 | g0024 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01167 | hp2 | a0003 | c0003 | t0004 | g0020 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01169 | hp2 | a0003 | c0003 | t0004 | g0020 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01175 | hp2 | a0004 | c0004 | t0005 | g0147 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01346 | hp2 | a0004 | c0004 | t0005 | g0039 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01433 | hp2 | a0003 | c0003 | t0004 | g0020 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | IBS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01928 | hp1 | a0004 | c0004 | t0005 | g0039 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01928 | hp2 | a0004 | c0004 | t0007 | g0145 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01952 | hp1 | a0001 | c0001 | t0015 | g0017 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01981 | hp2 | a0004 | c0004 | t0007 | g0023 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02015 | hp1 | a0002 | c0002 | t0003 | g0015 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02129 | hp1 | a0002 | c0002 | t0003 | g0052 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02155 | hp2 | a0002 | c0002 | t0012 | g0015 | EAS | CDX | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CDX | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0026 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0027 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02622 | hp1 | a0005 | c0005 | t0006 | g0022 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0027 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02717 | hp1 | a0007 | c0007 | t0002 | g0031 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02723 | hp2 | a0003 | c0003 | t0004 | g0043 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02735 | hp2 | a0008 | c0008 | t0001 | g0113 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02886 | hp1 | a0005 | c0005 | t0006 | g0022 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02922 | hp1 | a0007 | c0007 | t0002 | g0031 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03130 | hp1 | a0001 | c0009 | t0002 | g0021 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03195 | hp1 | a0005 | c0005 | t0006 | g0109 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0026 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03209 | hp1 | a0004 | c0004 | t0005 | g0045 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03239 | hp1 | a0004 | c0004 | t0007 | g0078 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03453 | hp2 | a0002 | c0002 | t0003 | g0047 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03486 | hp1 | a0001 | c0001 | t0011 | g0074 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03490 | hp2 | a0004 | c0004 | t0005 | g0144 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03492 | hp2 | a0004 | c0004 | t0005 | g0146 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03540 | hp2 | a0003 | c0003 | t0004 | g0042 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03710 | hp2 | a0001 | c0001 | t0013 | g0069 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | BEB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04228 | hp2 | a0009 | c0010 | t0001 | g0093 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | YRI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18522 | hp2 | a0004 | c0004 | t0005 | g0023 | AFR | YRI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18612 | hp1 | a0002 | c0002 | t0003 | g0016 | EAS | CHB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18906 | hp1 | a0003 | c0003 | t0004 | g0041 | AFR | YRI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | YRI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18941 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18944 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18946 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18950 | hp1 | a0002 | c0002 | t0003 | g0050 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18950 | hp2 | a0002 | c0002 | t0014 | g0016 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18953 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18954 | hp2 | a0002 | c0002 | t0003 | g0053 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18961 | hp2 | a0002 | c0002 | t0003 | g0016 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18964 | hp1 | a0002 | c0002 | t0003 | g0015 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18971 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18977 | hp1 | a0002 | c0002 | t0003 | g0025 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18981 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18988 | hp2 | a0002 | c0002 | t0003 | g0046 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18992 | hp2 | a0006 | c0006 | t0001 | g0013 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18994 | hp1 | a0002 | c0002 | t0003 | g0016 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19001 | hp2 | a0001 | c0001 | t0008 | g0104 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19009 | hp2 | a0006 | c0006 | t0001 | g0013 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19010 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | LWK | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | LWK | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19062 | hp1 | a0001 | c0001 | t0008 | g0103 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19064 | hp1 | a0002 | c0002 | t0003 | g0051 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19066 | hp2 | a0006 | c0006 | t0001 | g0013 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19077 | hp2 | a0002 | c0002 | t0003 | g0054 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19082 | hp2 | a0002 | c0002 | t0003 | g0015 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19085 | hp2 | a0002 | c0002 | t0003 | g0025 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19091 | hp1 | a0002 | c0002 | t0003 | g0055 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19091 | hp2 | a0002 | c0002 | t0003 | g0049 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | TSI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | TSI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA20905 | hp1 | a0004 | c0004 | t0005 | g0023 | SAS | GIH | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | GIH | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02559 | hp2 | a0005 | c0005 | t0006 | g0022 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | USA | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18955 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | USA | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | LWK | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0017 | REF | REF | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0019 | REF | REF | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:4830696 | G | A | 1 | a0008 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.61G>A | p.Glu21Lys | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/10 | 179/1613 | 61/963 | 21/320 | chr10 | 4830696 | |||
| chr10:4830738 | G | A | 1 | a0003 | 11 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(8): Show |
missense_variant | MODERATE | c.103G>A | p.Asp35Asn | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/10 | 221/1613 | 103/963 | 35/320 | chr10 | 4830738 | |||
| chr10:4830789 | T | G | 1 | a0007 | 2 | HG02717.hp1 HG02922.hp1 |
missense_variant | MODERATE | c.154T>G | p.Cys52Gly | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/10 | 272/1613 | 154/963 | 52/320 | chr10 | 4830789 | |||
| chr10:4833399 | A | G | 1 | a0002 | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
missense_variant | MODERATE | c.257A>G | p.Lys86Arg | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/10 | 375/1613 | 257/963 | 86/320 | chr10 | 4833399 | |||
| chr10:4835679 | C | G | 1 | a0005 | 4 | HG02559.hp2 HG02622.hp1 HG02886.hp1 others(1): Show |
missense_variant | MODERATE | c.329C>G | p.Pro110Arg | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/10 | 447/1613 | 329/963 | 110/320 | chr10 | 4835679 | |||
| chr10:4835787 | C | G | 1 | a0009 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.437C>G | p.Thr146Arg | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/10 | 555/1613 | 437/963 | 146/320 | chr10 | 4835787 | |||
| chr10:4847211 | C | T | 1 | a0004 | 11 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(8): Show |
stop_gained | HIGH | c.901C>T | p.Arg301* | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 9/10 | 1019/1613 | 901/963 | 301/320 | chr10 | 4847211 | |||
| chr10:4847493 | A | G | 1 | a0006 | 3 | NA18992.hp2 NA19009.hp2 NA19066.hp2 |
missense_variant | MODERATE | c.926A>G | p.Lys309Arg | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 1044/1613 | 926/963 | 309/320 | chr10 | 4847493 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:4830695 | C | A | 1 | a0002c0002 | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
synonymous_variant | LOW | c.60C>A | p.Thr20Thr | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/10 | 178/1613 | 60/963 | 20/320 | chr10 | 4830695 | |||
| chr10:4830695 | C | T | 1 | a0001c0011 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.60C>T | p.Thr20Thr | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/10 | 178/1613 | 60/963 | 20/320 | chr10 | 4830695 | |||
| chr10:4830719 | C | T | 1 | a0002c0002 | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
synonymous_variant | LOW | c.84C>T | p.Asp28Asp | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/10 | 202/1613 | 84/963 | 28/320 | chr10 | 4830719 | |||
| chr10:4837575 | C | G | 1 | a0001c0009 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.576C>G | p.Thr192Thr | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/10 | 694/1613 | 576/963 | 192/320 | chr10 | 4837575 | |||
| chr10:4839743 | A | G | 1 | a0002c0002 | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
synonymous_variant | LOW | c.597A>G | p.Pro199Pro | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/10 | 715/1613 | 597/963 | 199/320 | chr10 | 4839743 | |||
| chr10:4842450 | T | C | 1 | a0002c0002 | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
synonymous_variant | LOW | c.783T>C | p.Asn261Asn | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/10 | 901/1613 | 783/963 | 261/320 | chr10 | 4842450 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:4826253 | G | T | 15 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(12): Show |
265 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(262): Show |
5_prime_UTR_variant | MODIFIER | c.-72G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/10 | 72 | chr10 | 4826253 | ||||||
| chr10:4826287 | T | C | 1 | a0001c0001t0013 | 1 | HG03710.hp2 | 5_prime_UTR_variant | MODIFIER | c.-38T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/10 | 38 | chr10 | 4826287 | ||||||
| chr10:4826287 | T | TGCGGGGC others(1): Show |
2 | a0001c0001t0010 a0002c0002t0012 |
3 | HG02155.hp2 HG02280.hp2 HG03195.hp2 |
5_prime_UTR_variant | MODIFIER | c.-19_-12dupGGGGCGGC | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/10 | 11 | INFO_REALIGN_3_PRIME | chr10 | 4826287 | |||||
| chr10:4826287 | TGCGGGGC others(1): Show |
T | 1 | a0005c0005t0006 | 4 | HG02559.hp2 HG02622.hp1 HG02886.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-19_-12delGGGGCGGC | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/10 | 12 | INFO_REALIGN_3_PRIME | chr10 | 4826287 | |||||
| chr10:4826321 | G | A | 1 | a0001c0001t0009 | 2 | HG02615.hp1 HG02630.hp1 |
5_prime_UTR_variant | MODIFIER | c.-4G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/10 | 4 | chr10 | 4826321 | ||||||
| chr10:4847534 | C | CA | 3 | a0002c0002t0003 a0002c0002t0012 a0002c0002t0014 |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4_*5insA | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 5 | chr10 | 4847534 | ||||||
| chr10:4847538 | T | A | 1 | a0004c0004t0007 | 3 | HG01928.hp2 HG01981.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8T>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 8 | chr10 | 4847538 | ||||||
| chr10:4847540 | C | T | 2 | a0001c0001t0004 a0003c0003t0004 |
13 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*10C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 10 | chr10 | 4847540 | ||||||
| chr10:4847578 | T | C | 3 | a0002c0002t0003 a0002c0002t0012 a0002c0002t0014 |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*48T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 48 | chr10 | 4847578 | ||||||
| chr10:4847614 | C | T | 3 | a0002c0002t0003 a0002c0002t0012 a0002c0002t0014 |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*84C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 84 | chr10 | 4847614 | ||||||
| chr10:4847672 | C | G | 1 | a0001c0001t0011 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*142C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 142 | chr10 | 4847672 | ||||||
| chr10:4847782 | G | A | 3 | a0002c0002t0003 a0002c0002t0012 a0002c0002t0014 |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*252G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 252 | chr10 | 4847782 | ||||||
| chr10:4847882 | C | T | 1 | a0001c0001t0015 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*352C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 352 | chr10 | 4847882 | ||||||
| chr10:4847883 | G | A | 1 | a0001c0001t0008 | 3 | NA18944.hp1 NA19001.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*353G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 353 | chr10 | 4847883 | ||||||
| chr10:4847924 | A | T | 3 | a0002c0002t0003 a0002c0002t0012 a0002c0002t0014 |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*394A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 394 | chr10 | 4847924 | ||||||
| chr10:4847953 | C | T | 2 | a0004c0004t0005 a0004c0004t0007 |
11 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*423C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 423 | chr10 | 4847953 | ||||||
| chr10:4847994 | A | G | 3 | a0002c0002t0003 a0002c0002t0012 a0002c0002t0014 |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*464A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 464 | chr10 | 4847994 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:4826373 | T | C | 5 | a0003c0003t0004g0010 a0003c0003t0004g0020 a0003c0003t0004g0041 others(2): Show |
11 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.39+10T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826373 | |||||||
| chr10:4826589 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.39+226G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826589 | |||||||
| chr10:4826626 | G | A | 1 | a0004c0004t0005g0045 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.39+263G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826626 | |||||||
| chr10:4826631 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+268T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826631 | |||||||
| chr10:4826678 | T | C | 15 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(12): Show |
27 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.39+315T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826678 | |||||||
| chr10:4826687 | C | G | 9 | a0001c0001t0001g0040 a0004c0004t0005g0023 a0004c0004t0005g0039 others(6): Show |
12 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.39+324C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826687 | |||||||
| chr10:4826700 | C | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+337C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826700 | |||||||
| chr10:4826729 | G | T | 1 | a0001c0001t0001g0038 | 2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.39+366G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826729 | |||||||
| chr10:4826799 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+436G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826799 | |||||||
| chr10:4826839 | G | A | 1 | a0001c0001t0010g0026 | 2 | HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.39+476G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826839 | |||||||
| chr10:4826896 | C | T | 4 | a0001c0001t0001g0040 a0001c0001t0002g0014 a0001c0001t0002g0142 others(1): Show |
9 | HG01891.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.39+533C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826896 | |||||||
| chr10:4826956 | G | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.39+593G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826956 | |||||||
| chr10:4826981 | T | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.39+618T>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826981 | |||||||
| chr10:4827051 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+688T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827051 | |||||||
| chr10:4827075 | G | GA | 65 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(62): Show |
153 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.39+730dupA | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827075 | ||||||
| chr10:4827075 | G | GAA | 3 | a0001c0001t0001g0011 a0001c0001t0001g0070 a0004c0004t0005g0144 |
7 | HG01257.hp1 HG03490.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.39+729_39+730dupAA | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827075 | ||||||
| chr10:4827075 | G | GAAA | 9 | a0001c0001t0001g0004 a0001c0001t0001g0062 a0001c0001t0001g0063 others(6): Show |
19 | HG01261.hp2 HG02132.hp1 HG02738.hp2 others(16): Show |
intron_variant | MODIFIER | c.39+728_39+730dupAA others(1): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827075 | ||||||
| chr10:4827075 | G | GAAAA | 5 | a0001c0001t0001g0038 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
6 | HG02486.hp1 HG02559.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.39+727_39+730dupAA others(2): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827075 | ||||||
| chr10:4827075 | GAAAAAA | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0140 |
10 | HG00558.hp1 HG00621.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.39+725_39+730delAA others(4): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827075 | ||||||
| chr10:4827075 | GAAAAAAA | G | 3 | a0002c0002t0003g0008 a0002c0002t0003g0025 a0002c0002t0003g0053 |
10 | NA18941.hp1 NA18946.hp1 NA18953.hp1 others(7): Show |
intron_variant | MODIFIER | c.39+724_39+730delAA others(5): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827075 | ||||||
| chr10:4827075 | GAAAAAAA others(1): Show |
G | 5 | a0001c0001t0001g0040 a0001c0001t0002g0014 a0001c0001t0002g0141 others(2): Show |
10 | HG01891.hp1 HG01891.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.39+723_39+730delAA others(6): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827075 | ||||||
| chr10:4827088 | A | AG | 7 | a0001c0001t0001g0139 a0001c0001t0004g0037 a0003c0003t0004g0010 others(4): Show |
14 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.39+725_39+726insG | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827088 | |||||||
| chr10:4827301 | T | A | 1 | a0003c0003t0004g0020 | 3 | HG01167.hp2 HG01169.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.39+938T>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827301 | |||||||
| chr10:4827306 | ATTG | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0105 a0001c0001t0001g0138 |
12 | HG00140.hp1 HG01069.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.39+946_39+948delGT others(1): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827306 | ||||||
| chr10:4827318 | AAGATGTT others(177): Show |
A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+957_39+1140del | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827318 | ||||||
| chr10:4827422 | G | T | 1 | a0001c0001t0002g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.39+1059G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827422 | |||||||
| chr10:4827604 | T | TA | 8 | a0001c0001t0001g0062 a0001c0001t0001g0139 a0001c0001t0004g0037 others(5): Show |
15 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.39+1252dupA | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827604 | ||||||
| chr10:4827604 | TA | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+1252delA | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827604 | ||||||
| chr10:4827610 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.39+1247A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827610 | |||||||
| chr10:4827696 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG00597.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.39+1333G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827696 | |||||||
| chr10:4827706 | ATAT | A | 2 | a0002c0002t0003g0016 a0002c0002t0014g0016 |
4 | NA18612.hp1 NA18950.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+1348_39+1350del others(3): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827706 | ||||||
| chr10:4827730 | C | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+1367C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827730 | |||||||
| chr10:4827781 | C | T | 1 | a0002c0002t0003g0052 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.39+1418C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827781 | |||||||
| chr10:4827794 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+1431G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827794 | |||||||
| chr10:4827839 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(21): Show |
66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.39+1476G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827839 | |||||||
| chr10:4827849 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.39+1486T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827849 | |||||||
| chr10:4827893 | G | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+1530G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827893 | |||||||
| chr10:4827958 | ATATTC | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+1600_39+1604del others(5): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827958 | ||||||
| chr10:4828032 | C | A | 3 | a0001c0001t0001g0040 a0001c0001t0002g0014 a0001c0001t0002g0142 |
8 | HG01891.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.39+1669C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828032 | |||||||
| chr10:4828050 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(126): Show |
305 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.39+1687C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828050 | |||||||
| chr10:4828148 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+1785A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828148 | |||||||
| chr10:4828250 | G | A | 18 | a0001c0001t0009g0027 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+1887G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828250 | |||||||
| chr10:4828328 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(124): Show |
302 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.39+1965G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828328 | |||||||
| chr10:4828452 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): Show |
276 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.39+2089G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828452 | |||||||
| chr10:4828650 | A | C | 2 | a0001c0001t0001g0013 a0006c0006t0001g0013 |
5 | HG00558.hp2 HG00597.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-2025A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828650 | |||||||
| chr10:4828662 | C | T | 18 | a0001c0001t0009g0027 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.40-2013C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828662 | |||||||
| chr10:4828721 | T | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(21): Show |
66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.40-1954T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828721 | |||||||
| chr10:4828814 | G | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.40-1861G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828814 | |||||||
| chr10:4828860 | G | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(126): Show |
305 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.40-1815G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828860 | |||||||
| chr10:4828927 | G | A | 18 | a0001c0001t0009g0027 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.40-1748G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828927 | |||||||
| chr10:4828981 | TATC | T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
6 | HG02109.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-1689_40-1687del others(3): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4828981 | ||||||
| chr10:4829023 | C | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(126): Show |
305 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.40-1652C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829023 | |||||||
| chr10:4829058 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-1617C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829058 | |||||||
| chr10:4829242 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-1433G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829242 | |||||||
| chr10:4829264 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-1411T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829264 | |||||||
| chr10:4829399 | A | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-1276A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829399 | |||||||
| chr10:4829414 | G | T | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.40-1261G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829414 | |||||||
| chr10:4829462 | T | A | 1 | a0001c0001t0001g0077 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.40-1213T>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829462 | |||||||
| chr10:4829473 | G | A | 9 | a0004c0004t0005g0023 a0004c0004t0005g0039 a0004c0004t0005g0045 others(6): Show |
11 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.40-1202G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829473 | |||||||
| chr10:4829515 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.40-1160T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829515 | |||||||
| chr10:4829551 | A | AT | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-1117dupT | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4829551 | ||||||
| chr10:4829590 | C | CTT | 16 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(13): Show |
28 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.40-1078_40-1077dup others(2): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4829590 | ||||||
| chr10:4829590 | C | T | 1 | a0002c0002t0003g0054 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.40-1085C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829590 | |||||||
| chr10:4829605 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0009g0027 |
3 | HG02615.hp1 HG02630.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.40-1070C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829605 | |||||||
| chr10:4829696 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
312 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.40-979G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829696 | |||||||
| chr10:4829767 | G | A | 1 | a0001c0001t0002g0125 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.40-908G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829767 | |||||||
| chr10:4829930 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-745C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829930 | |||||||
| chr10:4830021 | G | A | 3 | a0001c0001t0002g0032 a0001c0001t0002g0124 a0001c0001t0011g0074 |
4 | HG01243.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-654G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830021 | |||||||
| chr10:4830022 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-653A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830022 | |||||||
| chr10:4830053 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0059 others(11): Show |
24 | HG01261.hp2 HG02109.hp2 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.40-622C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830053 | |||||||
| chr10:4830071 | A | C | 1 | a0002c0002t0003g0024 | 2 | HG00741.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.40-604A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830071 | |||||||
| chr10:4830131 | C | T | 4 | a0001c0001t0002g0032 a0001c0001t0002g0124 a0001c0001t0002g0143 others(1): Show |
5 | HG01243.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-544C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830131 | |||||||
| chr10:4830229 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-446A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830229 | |||||||
| chr10:4830240 | A | G | 2 | a0001c0001t0009g0027 a0007c0007t0002g0031 |
4 | HG02615.hp1 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-435A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830240 | |||||||
| chr10:4830256 | A | G | 1 | a0001c0001t0008g0104 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.40-419A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830256 | |||||||
| chr10:4830332 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
314 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(311): Show |
intron_variant | MODIFIER | c.40-343A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830332 | |||||||
| chr10:4830347 | T | TC | 10 | a0001c0001t0001g0136 a0004c0004t0005g0023 a0004c0004t0005g0039 others(7): Show |
12 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.40-328_40-327insC | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830347 | |||||||
| chr10:4830364 | C | G | 24 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(21): Show |
66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.40-311C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830364 | |||||||
| chr10:4830381 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
352 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(349): Show |
intron_variant | MODIFIER | c.40-294G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830381 | |||||||
| chr10:4830425 | C | T | 7 | a0001c0001t0001g0139 a0001c0001t0004g0037 a0003c0003t0004g0010 others(4): Show |
14 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.40-250C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830425 | |||||||
| chr10:4830459 | GT | G | 18 | a0001c0001t0009g0027 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.40-207delT | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4830459 | ||||||
| chr10:4830495 | T | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-180T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830495 | |||||||
| chr10:4830577 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-98T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830577 | |||||||
| chr10:4830630 | A | C | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.40-45A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830630 | |||||||
| chr10:4830640 | C | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.40-35C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830640 | |||||||
| chr10:4830845 | A | G | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
splice_region_variant&intron_variant | LOW | c.207+3A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4830845 | |||||||
| chr10:4830914 | T | C | 10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0017 others(7): Show |
30 | HG00140.hp1 HG01069.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.207+72T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4830914 | |||||||
| chr10:4831072 | A | T | 2 | a0001c0001t0008g0103 a0002c0002t0003g0053 |
2 | NA18954.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.207+230A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831072 | |||||||
| chr10:4831331 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
314 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(311): Show |
intron_variant | MODIFIER | c.207+489T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831331 | |||||||
| chr10:4831350 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+508G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831350 | |||||||
| chr10:4831466 | G | A | 2 | a0001c0001t0002g0143 a0001c0001t0009g0027 |
3 | HG02615.hp1 HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.207+624G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831466 | |||||||
| chr10:4831492 | A | C | 18 | a0001c0001t0009g0027 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.207+650A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831492 | |||||||
| chr10:4831493 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+651G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831493 | |||||||
| chr10:4831511 | G | C | 18 | a0001c0001t0009g0027 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.207+669G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831511 | |||||||
| chr10:4831530 | G | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+688G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831530 | |||||||
| chr10:4831534 | C | T | 18 | a0001c0001t0009g0027 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.207+692C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831534 | |||||||
| chr10:4831565 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.207+723A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831565 | |||||||
| chr10:4831574 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+732T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831574 | |||||||
| chr10:4831734 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+892T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831734 | |||||||
| chr10:4831744 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+902T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831744 | |||||||
| chr10:4831745 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+903G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831745 | |||||||
| chr10:4831752 | A | G | 18 | a0001c0001t0009g0027 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.207+910A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831752 | |||||||
| chr10:4831827 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+985A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831827 | |||||||
| chr10:4831852 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+1010A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831852 | |||||||
| chr10:4831876 | A | G | 18 | a0001c0001t0009g0027 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.207+1034A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831876 | |||||||
| chr10:4831933 | A | T | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.207+1091A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831933 | |||||||
| chr10:4832022 | G | T | 9 | a0004c0004t0005g0023 a0004c0004t0005g0039 a0004c0004t0005g0045 others(6): Show |
11 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.207+1180G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832022 | |||||||
| chr10:4832120 | G | GT | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
312 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.208-1229dupT | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 4832120 | ||||||
| chr10:4832208 | C | T | 1 | a0001c0001t0010g0026 | 2 | HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.208-1142C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832208 | |||||||
| chr10:4832335 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.208-1015G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832335 | |||||||
| chr10:4832397 | G | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.208-953G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832397 | |||||||
| chr10:4832520 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.208-830G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832520 | |||||||
| chr10:4832602 | A | G | 9 | a0004c0004t0005g0023 a0004c0004t0005g0039 a0004c0004t0005g0045 others(6): Show |
11 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.208-748A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832602 | |||||||
| chr10:4832607 | A | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.208-743A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832607 | |||||||
| chr10:4832607 | A | T | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.208-743A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832607 | |||||||
| chr10:4832644 | A | G | 18 | a0001c0001t0009g0027 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.208-706A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832644 | |||||||
| chr10:4832679 | G | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(22): Show |
68 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.208-671G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832679 | |||||||
| chr10:4832724 | TTTTACTT others(8): Show |
T | 24 | a0001c0001t0004g0037 a0001c0001t0009g0027 a0002c0002t0003g0008 others(21): Show |
44 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.208-601_208-587del others(15): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 4832724 | ||||||
| chr10:4832875 | G | A | 18 | a0001c0001t0009g0027 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.208-475G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832875 | |||||||
| chr10:4832880 | C | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.208-470C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832880 | |||||||
| chr10:4832958 | T | C | 18 | a0001c0001t0009g0027 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.208-392T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832958 | |||||||
| chr10:4832997 | G | A | 2 | a0002c0002t0003g0047 a0002c0002t0003g0048 |
2 | HG00642.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.208-353G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832997 | |||||||
| chr10:4833043 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.208-307T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4833043 | |||||||
| chr10:4833070 | A | G | 24 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(21): Show |
66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.208-280A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4833070 | |||||||
| chr10:4833079 | A | G | 1 | a0001c0001t0002g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.208-271A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4833079 | |||||||
| chr10:4833084 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.208-266C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4833084 | |||||||
| chr10:4833172 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.208-178C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4833172 | |||||||
| chr10:4833208 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.208-142C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4833208 | |||||||
| chr10:4833217 | T | C | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.208-133T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4833217 | |||||||
| chr10:4833249 | G | T | 1 | a0001c0001t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.208-101G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4833249 | |||||||
| chr10:4833263 | C | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0061 a0001c0001t0001g0062 others(7): Show |
20 | HG01261.hp2 HG02132.hp1 HG02738.hp2 others(17): Show |
intron_variant | MODIFIER | c.208-87C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4833263 | |||||||
| chr10:4833472 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
splice_region_variant&intron_variant | LOW | c.324+6G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4833472 | |||||||
| chr10:4833637 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.324+171C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4833637 | |||||||
| chr10:4833682 | G | T | 1 | a0001c0001t0010g0026 | 2 | HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.324+216G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4833682 | |||||||
| chr10:4833702 | G | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(18): Show |
61 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.324+236G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4833702 | |||||||
| chr10:4833731 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.324+265A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4833731 | |||||||
| chr10:4833987 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.324+521A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4833987 | |||||||
| chr10:4834028 | C | T | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.324+562C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834028 | |||||||
| chr10:4834030 | T | G | 1 | a0002c0002t0003g0054 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.324+564T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834030 | |||||||
| chr10:4834154 | C | T | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.324+688C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834154 | |||||||
| chr10:4834183 | G | T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
6 | HG02109.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+717G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834183 | |||||||
| chr10:4834211 | C | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.324+745C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834211 | |||||||
| chr10:4834377 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.324+911T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834377 | |||||||
| chr10:4834382 | G | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.324+916G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834382 | |||||||
| chr10:4834434 | A | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
156 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.324+968A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834434 | |||||||
| chr10:4834691 | T | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(21): Show |
66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.325-984T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834691 | |||||||
| chr10:4834768 | G | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.325-907G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834768 | |||||||
| chr10:4834779 | A | G | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.325-896A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834779 | |||||||
| chr10:4834781 | A | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.325-894A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834781 | |||||||
| chr10:4834898 | A | G | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.325-777A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834898 | |||||||
| chr10:4834909 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.325-766C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834909 | |||||||
| chr10:4834923 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.325-752G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834923 | |||||||
| chr10:4835121 | A | T | 1 | a0001c0001t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.325-554A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835121 | |||||||
| chr10:4835167 | A | G | 18 | a0001c0001t0009g0027 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.325-508A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835167 | |||||||
| chr10:4835200 | A | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
314 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(311): Show |
intron_variant | MODIFIER | c.325-475A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835200 | |||||||
| chr10:4835267 | A | C | 1 | a0001c0001t0001g0028 | 2 | HG01106.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.325-408A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835267 | |||||||
| chr10:4835330 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(21): Show |
66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.325-345G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835330 | |||||||
| chr10:4835388 | T | C | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.325-287T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835388 | |||||||
| chr10:4835443 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.325-232C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835443 | |||||||
| chr10:4835524 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.325-151T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835524 | |||||||
| chr10:4835544 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.325-131G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835544 | |||||||
| chr10:4835618 | G | T | 2 | a0001c0001t0001g0073 a0001c0001t0009g0027 |
3 | HG02615.hp1 HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.325-57G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835618 | |||||||
| chr10:4835622 | T | TTTTTG | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
148 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.325-33_325-29dupGT others(3): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr10 | 4835622 | ||||||
| chr10:4835624 | T | G | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.325-51T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835624 | |||||||
| chr10:4835625 | T | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.325-50T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835625 | |||||||
| chr10:4835627 | G | T | 18 | a0001c0001t0009g0027 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.325-48G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835627 | |||||||
| chr10:4835628 | T | G | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.325-47T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835628 | |||||||
| chr10:4835633 | TTTTG | T | 16 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(13): Show |
28 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.325-38_325-35delGT others(2): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr10 | 4835633 | ||||||
| chr10:4835642 | G | T | 18 | a0001c0001t0009g0027 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.325-33G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835642 | |||||||
| chr10:4835889 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+80G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4835889 | |||||||
| chr10:4835940 | A | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
314 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(311): Show |
intron_variant | MODIFIER | c.459+131A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4835940 | |||||||
| chr10:4835955 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+146C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4835955 | |||||||
| chr10:4836012 | T | C | 42 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(39): Show |
97 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.459+203T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836012 | |||||||
| chr10:4836040 | A | G | 18 | a0001c0001t0009g0027 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.459+231A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836040 | |||||||
| chr10:4836083 | T | G | 18 | a0001c0001t0009g0027 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.459+274T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836083 | |||||||
| chr10:4836123 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+314C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836123 | |||||||
| chr10:4836127 | T | C | 18 | a0001c0001t0009g0027 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.459+318T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836127 | |||||||
| chr10:4836129 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+320C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836129 | |||||||
| chr10:4836217 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+408T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836217 | |||||||
| chr10:4836218 | C | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+409C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836218 | |||||||
| chr10:4836239 | A | G | 10 | a0001c0001t0001g0136 a0004c0004t0005g0023 a0004c0004t0005g0039 others(7): Show |
12 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.459+430A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836239 | |||||||
| chr10:4836349 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+540A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836349 | |||||||
| chr10:4836372 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.459+563G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836372 | |||||||
| chr10:4836403 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
312 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.459+594T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836403 | |||||||
| chr10:4836410 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0013g0069 |
2 | HG02738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.459+601C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836410 | |||||||
| chr10:4836472 | A | G | 14 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0024 others(11): Show |
24 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.459+663A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836472 | |||||||
| chr10:4836514 | G | T | 1 | a0001c0001t0010g0026 | 2 | HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.459+705G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836514 | |||||||
| chr10:4836543 | G | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.459+734G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836543 | |||||||
| chr10:4836687 | G | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0071 a0001c0001t0001g0106 others(13): Show |
53 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.460-772G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836687 | |||||||
| chr10:4836731 | G | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
312 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.460-728G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836731 | |||||||
| chr10:4836739 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.460-720A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836739 | |||||||
| chr10:4836769 | G | A | 2 | a0002c0002t0003g0054 a0002c0002t0003g0055 |
2 | NA19077.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.460-690G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836769 | |||||||
| chr10:4836780 | G | A | 18 | a0001c0001t0001g0063 a0001c0001t0001g0136 a0001c0001t0004g0037 others(15): Show |
27 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.460-679G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836780 | |||||||
| chr10:4836834 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.460-625C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836834 | |||||||
| chr10:4836903 | A | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(57): Show |
162 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.460-556A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836903 | |||||||
| chr10:4837055 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.460-404G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4837055 | |||||||
| chr10:4837180 | C | G | 10 | a0001c0001t0001g0004 a0001c0001t0001g0061 a0001c0001t0001g0062 others(7): Show |
20 | HG01261.hp2 HG02132.hp1 HG02738.hp2 others(17): Show |
intron_variant | MODIFIER | c.460-279C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4837180 | |||||||
| chr10:4837188 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.460-271C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4837188 | |||||||
| chr10:4837221 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.460-238T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4837221 | |||||||
| chr10:4837233 | A | G | 24 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(21): Show |
66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.460-226A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4837233 | |||||||
| chr10:4837273 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
312 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.460-186T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4837273 | |||||||
| chr10:4837376 | A | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.460-83A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4837376 | |||||||
| chr10:4837447 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.460-12G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4837447 | |||||||
| chr10:4837723 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.582+142T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4837723 | |||||||
| chr10:4837885 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.582+304T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4837885 | |||||||
| chr10:4837971 | G | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
314 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(311): Show |
intron_variant | MODIFIER | c.582+390G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4837971 | |||||||
| chr10:4838046 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.582+465C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838046 | |||||||
| chr10:4838049 | T | C | 2 | a0001c0001t0002g0075 a0001c0001t0002g0126 |
2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.582+468T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838049 | |||||||
| chr10:4838099 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.582+518T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838099 | |||||||
| chr10:4838130 | A | C | 1 | a0001c0001t0002g0133 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.582+549A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838130 | |||||||
| chr10:4838182 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(125): Show |
304 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.582+601T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838182 | |||||||
| chr10:4838207 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.582+626G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838207 | |||||||
| chr10:4838232 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.582+651G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838232 | |||||||
| chr10:4838244 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.582+663A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838244 | |||||||
| chr10:4838282 | T | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(21): Show |
66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.582+701T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838282 | |||||||
| chr10:4838423 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.582+842T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838423 | |||||||
| chr10:4838468 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.582+887G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838468 | |||||||
| chr10:4838488 | G | A | 1 | a0001c0001t0010g0026 | 2 | HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.582+907G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838488 | |||||||
| chr10:4838496 | T | C | 20 | a0001c0001t0001g0009 a0001c0001t0001g0087 a0001c0001t0001g0088 others(17): Show |
37 | HG00621.hp1 HG00642.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.582+915T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838496 | |||||||
| chr10:4838689 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.583-1040C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838689 | |||||||
| chr10:4838936 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0058 |
3 | HG02559.hp1 HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.583-793G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838936 | |||||||
| chr10:4839022 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.583-707C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839022 | |||||||
| chr10:4839299 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0015g0017 |
3 | HG01952.hp1 HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.583-430A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839299 | |||||||
| chr10:4839354 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.583-375G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839354 | |||||||
| chr10:4839419 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.583-310G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839419 | |||||||
| chr10:4839453 | TTATC | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(21): Show |
66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.583-274_583-271del others(4): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 4839453 | ||||||
| chr10:4839490 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.583-239G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839490 | |||||||
| chr10:4839507 | A | C | 1 | a0001c0001t0002g0132 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.583-222A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839507 | |||||||
| chr10:4839586 | C | T | 2 | a0001c0001t0002g0032 a0001c0001t0002g0124 |
3 | HG01243.hp1 HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.583-143C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839586 | |||||||
| chr10:4839596 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.583-133G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839596 | |||||||
| chr10:4839631 | C | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.583-98C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839631 | |||||||
| chr10:4839654 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.583-75C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839654 | |||||||
| chr10:4839675 | C | T | 1 | a0003c0003t0004g0020 | 3 | HG01167.hp2 HG01169.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.583-54C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839675 | |||||||
| chr10:4839686 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.583-43C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839686 | |||||||
| chr10:4839889 | T | C | 1 | a0002c0002t0003g0050 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.680+63T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4839889 | |||||||
| chr10:4839903 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.680+77C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4839903 | |||||||
| chr10:4840108 | A | G | 3 | a0001c0001t0002g0032 a0001c0001t0002g0124 a0001c0001t0011g0074 |
4 | HG01243.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.680+282A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840108 | |||||||
| chr10:4840118 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.680+292C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840118 | |||||||
| chr10:4840173 | G | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(22): Show |
68 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.680+347G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840173 | |||||||
| chr10:4840197 | C | T | 11 | a0002c0002t0003g0008 a0002c0002t0003g0016 a0002c0002t0003g0025 others(8): Show |
20 | NA18612.hp1 NA18941.hp1 NA18946.hp1 others(17): Show |
intron_variant | MODIFIER | c.680+371C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840197 | |||||||
| chr10:4840215 | G | C | 1 | a0001c0001t0002g0128 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.680+389G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840215 | |||||||
| chr10:4840306 | C | G | 1 | a0001c0001t0002g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.680+480C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840306 | |||||||
| chr10:4840341 | A | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(21): Show |
66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.680+515A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840341 | |||||||
| chr10:4840342 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(21): Show |
66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.680+516G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840342 | |||||||
| chr10:4840365 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.680+539G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840365 | |||||||
| chr10:4840521 | A | G | 5 | a0001c0001t0001g0139 a0001c0001t0002g0032 a0001c0001t0002g0124 others(2): Show |
6 | HG01243.hp1 HG02886.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.680+695A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840521 | |||||||
| chr10:4840532 | G | C | 6 | a0001c0001t0004g0037 a0003c0003t0004g0010 a0003c0003t0004g0020 others(3): Show |
14 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.680+706G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840532 | |||||||
| chr10:4840594 | C | T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
6 | HG02109.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.680+768C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840594 | |||||||
| chr10:4840628 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.680+802C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840628 | |||||||
| chr10:4840782 | T | G | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.680+956T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840782 | |||||||
| chr10:4840866 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.681-919G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840866 | |||||||
| chr10:4840900 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(21): Show |
66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.681-885G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840900 | |||||||
| chr10:4841132 | G | C | 1 | a0001c0001t0010g0026 | 2 | HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.681-653G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841132 | |||||||
| chr10:4841190 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.681-595C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841190 | |||||||
| chr10:4841195 | C | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.681-590C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841195 | |||||||
| chr10:4841274 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.681-511C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841274 | |||||||
| chr10:4841282 | T | G | 1 | a0001c0001t0002g0129 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.681-503T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841282 | |||||||
| chr10:4841322 | A | G | 3 | a0001c0001t0001g0040 a0001c0001t0002g0014 a0001c0001t0002g0142 |
8 | HG01891.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-463A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841322 | |||||||
| chr10:4841475 | C | CA | 41 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(38): Show |
95 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.681-310_681-309ins others(1): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841475 | |||||||
| chr10:4841516 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.681-269G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841516 | |||||||
| chr10:4841533 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.681-252T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841533 | |||||||
| chr10:4841544 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.681-241A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841544 | |||||||
| chr10:4841558 | T | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.681-227T>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841558 | |||||||
| chr10:4841572 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0061 a0001c0001t0001g0062 others(7): Show |
20 | HG01261.hp2 HG02132.hp1 HG02738.hp2 others(17): Show |
intron_variant | MODIFIER | c.681-213G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841572 | |||||||
| chr10:4841678 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.681-107T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841678 | |||||||
| chr10:4841755 | G | T | 1 | a0001c0001t0002g0142 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.681-30G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841755 | |||||||
| chr10:4841874 | G | C | 1 | a0001c0001t0002g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.753+17G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4841874 | |||||||
| chr10:4841884 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.753+27A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4841884 | |||||||
| chr10:4841907 | A | G | 1 | a0004c0004t0005g0147 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.753+50A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4841907 | |||||||
| chr10:4841912 | C | T | 1 | a0002c0002t0003g0048 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.753+55C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4841912 | |||||||
| chr10:4841968 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.753+111G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4841968 | |||||||
| chr10:4842019 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.753+162C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4842019 | |||||||
| chr10:4842025 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.753+168T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4842025 | |||||||
| chr10:4842052 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.753+195C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4842052 | |||||||
| chr10:4842095 | C | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0070 a0006c0006t0001g0013 |
6 | HG00558.hp2 HG00597.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.753+238C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4842095 | |||||||
| chr10:4842130 | A | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.753+273A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4842130 | |||||||
| chr10:4842234 | C | G | 7 | a0001c0001t0001g0139 a0001c0001t0002g0032 a0001c0001t0002g0075 others(4): Show |
8 | HG01243.hp1 HG02647.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.754-187C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4842234 | |||||||
| chr10:4842255 | G | T | 9 | a0004c0004t0005g0023 a0004c0004t0005g0039 a0004c0004t0005g0045 others(6): Show |
11 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.754-166G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4842255 | |||||||
| chr10:4842529 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+25G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842529 | |||||||
| chr10:4842531 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.837+27C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842531 | |||||||
| chr10:4842592 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(133): Show |
314 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(311): Show |
intron_variant | MODIFIER | c.837+88T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842592 | |||||||
| chr10:4842593 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.837+89G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842593 | |||||||
| chr10:4842608 | A | G | 41 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(38): Show |
95 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.837+104A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842608 | |||||||
| chr10:4842616 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+112T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842616 | |||||||
| chr10:4842618 | C | T | 3 | a0001c0001t0002g0032 a0001c0001t0002g0124 a0001c0001t0011g0074 |
4 | HG01243.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+114C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842618 | |||||||
| chr10:4842652 | T | TC | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+151dupC | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr10 | 4842652 | ||||||
| chr10:4842736 | A | C | 1 | a0001c0001t0001g0079 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.837+232A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842736 | |||||||
| chr10:4842771 | T | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(38): Show |
95 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.837+267T>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842771 | |||||||
| chr10:4842854 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0058 others(12): Show |
26 | HG01261.hp2 HG02109.hp2 HG02132.hp1 others(23): Show |
intron_variant | MODIFIER | c.837+350G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842854 | |||||||
| chr10:4842858 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+354A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842858 | |||||||
| chr10:4842941 | CT | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(21): Show |
66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.837+440delT | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr10 | 4842941 | ||||||
| chr10:4843025 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+521C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843025 | |||||||
| chr10:4843026 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.837+522G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843026 | |||||||
| chr10:4843039 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+535A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843039 | |||||||
| chr10:4843056 | T | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0091 |
2 | HG02071.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.837+552T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843056 | |||||||
| chr10:4843136 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.837+632A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843136 | |||||||
| chr10:4843151 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.837+647C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843151 | |||||||
| chr10:4843207 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+703C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843207 | |||||||
| chr10:4843302 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0002g0014 a0001c0001t0002g0142 |
8 | HG01891.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.837+798G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843302 | |||||||
| chr10:4843313 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+809G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843313 | |||||||
| chr10:4843321 | A | T | 1 | a0001c0001t0001g0095 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.837+817A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843321 | |||||||
| chr10:4843337 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.837+833C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843337 | |||||||
| chr10:4843340 | A | G | 2 | a0004c0004t0005g0144 a0004c0004t0005g0146 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.837+836A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843340 | |||||||
| chr10:4843344 | A | C | 1 | a0001c0001t0002g0035 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.837+840A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843344 | |||||||
| chr10:4843423 | T | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0061 a0001c0001t0001g0062 others(7): Show |
20 | HG01261.hp2 HG02132.hp1 HG02738.hp2 others(17): Show |
intron_variant | MODIFIER | c.837+919T>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843423 | |||||||
| chr10:4843428 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.837+924G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843428 | |||||||
| chr10:4843458 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+954T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843458 | |||||||
| chr10:4843614 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
156 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.837+1110G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843614 | |||||||
| chr10:4843618 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.837+1114T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843618 | |||||||
| chr10:4843642 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+1138A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843642 | |||||||
| chr10:4843651 | G | T | 3 | a0001c0001t0001g0040 a0001c0001t0002g0014 a0001c0001t0002g0142 |
8 | HG01891.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.837+1147G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843651 | |||||||
| chr10:4843727 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+1223A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843727 | |||||||
| chr10:4843742 | A | C | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.837+1238A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843742 | |||||||
| chr10:4843743 | C | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.837+1239C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843743 | |||||||
| chr10:4843829 | C | T | 1 | a0007c0007t0002g0031 | 2 | HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.837+1325C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843829 | |||||||
| chr10:4843848 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.837+1344G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843848 | |||||||
| chr10:4843908 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+1404G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843908 | |||||||
| chr10:4843925 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+1421A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843925 | |||||||
| chr10:4843976 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+1472A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843976 | |||||||
| chr10:4844059 | G | A | 2 | a0003c0003t0004g0041 a0003c0003t0004g0042 |
2 | HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.837+1555G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844059 | |||||||
| chr10:4844091 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.837+1587C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844091 | |||||||
| chr10:4844093 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.837+1589C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844093 | |||||||
| chr10:4844125 | A | C | 1 | a0001c0001t0008g0103 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.837+1621A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844125 | |||||||
| chr10:4844126 | G | T | 1 | a0001c0001t0008g0103 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.837+1622G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844126 | |||||||
| chr10:4844136 | C | T | 1 | a0001c0001t0010g0026 | 2 | HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.837+1632C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844136 | |||||||
| chr10:4844171 | G | A | 5 | a0001c0001t0001g0038 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
6 | HG02109.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.837+1667G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844171 | |||||||
| chr10:4844225 | A | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+1721A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844225 | |||||||
| chr10:4844237 | G | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.837+1733G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844237 | |||||||
| chr10:4844314 | A | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0071 a0001c0001t0001g0106 others(13): Show |
53 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.837+1810A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844314 | |||||||
| chr10:4844337 | C | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(18): Show |
61 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.837+1833C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844337 | |||||||
| chr10:4844409 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.837+1905C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844409 | |||||||
| chr10:4844410 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+1906G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844410 | |||||||
| chr10:4844427 | G | A | 1 | a0003c0003t0004g0041 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.837+1923G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844427 | |||||||
| chr10:4844431 | T | C | 1 | a0001c0001t0001g0029 | 2 | HG03654.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.837+1927T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844431 | |||||||
| chr10:4844449 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+1945T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844449 | |||||||
| chr10:4844453 | T | G | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.837+1949T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844453 | |||||||
| chr10:4844459 | G | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+1955G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844459 | |||||||
| chr10:4844535 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+2031G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844535 | |||||||
| chr10:4844540 | G | C | 4 | a0004c0004t0005g0039 a0004c0004t0005g0144 a0004c0004t0005g0146 others(1): Show |
5 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.837+2036G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844540 | |||||||
| chr10:4844693 | G | A | 1 | a0005c0005t0006g0022 | 3 | HG02559.hp2 HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.837+2189G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844693 | |||||||
| chr10:4844713 | G | GTGAGCTA others(157): Show |
17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+2249_837+2250i others(166): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr10 | 4844713 | ||||||
| chr10:4844754 | G | A | 1 | a0004c0004t0007g0145 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.837+2250G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844754 | |||||||
| chr10:4844865 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0081 |
3 | NA18973.hp2 NA18998.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.838-2283C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844865 | |||||||
| chr10:4844866 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.838-2282G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844866 | |||||||
| chr10:4844900 | C | T | 18 | a0001c0001t0001g0122 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
30 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.838-2248C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844900 | |||||||
| chr10:4844931 | G | T | 3 | a0001c0001t0001g0108 a0005c0005t0006g0022 a0005c0005t0006g0109 |
5 | HG02055.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.838-2217G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844931 | |||||||
| chr10:4844950 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-2198T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844950 | |||||||
| chr10:4845001 | G | C | 1 | a0001c0001t0001g0112 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.838-2147G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845001 | |||||||
| chr10:4845063 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-2085G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845063 | |||||||
| chr10:4845103 | C | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-2045C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845103 | |||||||
| chr10:4845104 | C | T | 18 | a0001c0001t0001g0066 a0002c0002t0003g0008 a0002c0002t0003g0015 others(15): Show |
30 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.838-2044C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845104 | |||||||
| chr10:4845130 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-2018T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845130 | |||||||
| chr10:4845148 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.838-2000C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845148 | |||||||
| chr10:4845164 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1984A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845164 | |||||||
| chr10:4845199 | A | G | 58 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(55): Show |
125 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.838-1949A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845199 | |||||||
| chr10:4845202 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1946C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845202 | |||||||
| chr10:4845207 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1941C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845207 | |||||||
| chr10:4845236 | A | T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
6 | HG02109.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.838-1912A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845236 | |||||||
| chr10:4845268 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1880G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845268 | |||||||
| chr10:4845278 | G | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
180 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.838-1870G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845278 | |||||||
| chr10:4845279 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1869A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845279 | |||||||
| chr10:4845297 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.838-1851C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845297 | |||||||
| chr10:4845329 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1819G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845329 | |||||||
| chr10:4845340 | C | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
181 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.838-1808C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845340 | |||||||
| chr10:4845373 | C | T | 5 | a0001c0001t0001g0139 a0001c0001t0002g0032 a0001c0001t0002g0124 others(2): Show |
6 | HG01243.hp1 HG02886.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.838-1775C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845373 | |||||||
| chr10:4845390 | C | T | 2 | a0005c0005t0006g0022 a0005c0005t0006g0109 |
4 | HG02559.hp2 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.838-1758C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845390 | |||||||
| chr10:4845398 | G | A | 1 | a0001c0001t0002g0130 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.838-1750G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845398 | |||||||
| chr10:4845442 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1706T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845442 | |||||||
| chr10:4845448 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1700T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845448 | |||||||
| chr10:4845453 | A | AGGGCTGC others(55): Show |
1 | a0001c0001t0002g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.838-1690_838-1629d others(64): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr10 | 4845453 | ||||||
| chr10:4845453 | AGGGCTGC others(24): Show |
A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
210 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.838-1659_838-1629d others(33): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr10 | 4845453 | ||||||
| chr10:4845546 | G | A | 2 | a0003c0003t0004g0010 a0003c0003t0004g0020 |
8 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.838-1602G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845546 | |||||||
| chr10:4845621 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1527C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845621 | |||||||
| chr10:4845664 | G | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0058 |
3 | HG02559.hp1 HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.838-1484G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845664 | |||||||
| chr10:4845680 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.838-1468G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845680 | |||||||
| chr10:4845698 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.838-1450C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845698 | |||||||
| chr10:4845724 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.838-1424G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845724 | |||||||
| chr10:4845743 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1405T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845743 | |||||||
| chr10:4845796 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(21): Show |
66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.838-1352G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845796 | |||||||
| chr10:4845813 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.838-1335G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845813 | |||||||
| chr10:4845892 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.838-1256G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845892 | |||||||
| chr10:4845895 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.838-1253G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845895 | |||||||
| chr10:4845908 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.838-1240C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845908 | |||||||
| chr10:4845948 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1200A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845948 | |||||||
| chr10:4845957 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1191A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845957 | |||||||
| chr10:4846002 | C | T | 1 | a0007c0007t0002g0031 | 2 | HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.838-1146C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846002 | |||||||
| chr10:4846030 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(22): Show |
67 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.838-1118C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846030 | |||||||
| chr10:4846087 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1061T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846087 | |||||||
| chr10:4846142 | A | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1006A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846142 | |||||||
| chr10:4846157 | G | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0089 |
7 | HG01069.hp2 HG01071.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.838-991G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846157 | |||||||
| chr10:4846233 | A | G | 2 | a0001c0001t0001g0114 a0008c0008t0001g0113 |
2 | HG02523.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.838-915A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846233 | |||||||
| chr10:4846263 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-885G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846263 | |||||||
| chr10:4846284 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-864C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846284 | |||||||
| chr10:4846290 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0092 |
2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.838-858G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846290 | |||||||
| chr10:4846318 | G | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-830G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846318 | |||||||
| chr10:4846361 | G | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
147 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.838-787G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846361 | |||||||
| chr10:4846382 | C | G | 1 | a0001c0001t0008g0104 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.838-766C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846382 | |||||||
| chr10:4846399 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.838-749T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846399 | |||||||
| chr10:4846449 | C | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-699C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846449 | |||||||
| chr10:4846454 | G | A | 3 | a0001c0001t0002g0032 a0001c0001t0002g0124 a0001c0001t0011g0074 |
4 | HG01243.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.838-694G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846454 | |||||||
| chr10:4846492 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.838-656T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846492 | |||||||
| chr10:4846530 | G | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.838-618G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846530 | |||||||
| chr10:4846549 | C | CTTT | 16 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(13): Show |
27 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.838-587_838-585dup others(3): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr10 | 4846549 | ||||||
| chr10:4846590 | A | G | 24 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0071 others(21): Show |
66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.838-558A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846590 | |||||||
| chr10:4846614 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-534C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846614 | |||||||
| chr10:4846651 | T | C | 1 | a0009c0010t0001g0093 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.838-497T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846651 | |||||||
| chr10:4846717 | T | A | 1 | a0001c0001t0001g0105 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.838-431T>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846717 | |||||||
| chr10:4846769 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-379C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846769 | |||||||
| chr10:4846824 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
209 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.838-324G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846824 | |||||||
| chr10:4846828 | A | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-320A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846828 | |||||||
| chr10:4846833 | C | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-315C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846833 | |||||||
| chr10:4846838 | C | A | 1 | a0007c0007t0002g0031 | 2 | HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.838-310C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846838 | |||||||
| chr10:4846844 | G | A | 1 | a0008c0008t0001g0113 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.838-304G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846844 | |||||||
| chr10:4846920 | G | C | 1 | a0001c0001t0002g0033 | 2 | HG02040.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.838-228G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846920 | |||||||
| chr10:4846947 | C | A | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-201C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846947 | |||||||
| chr10:4847006 | G | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.838-142G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4847006 | |||||||
| chr10:4847069 | C | T | 1 | a0001c0001t0002g0034 | 2 | HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.838-79C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4847069 | |||||||
| chr10:4847073 | G | A | 14 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(11): Show |
25 | HG02015.hp1 HG02129.hp1 HG02155.hp2 others(22): Show |
intron_variant | MODIFIER | c.838-75G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4847073 | |||||||
| chr10:4847115 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.838-33A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4847115 | |||||||
| chr10:4847283 | G | T | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.920+53G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 9/9 | chr10 | 4847283 | |||||||
| chr10:4847312 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.920+82C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 9/9 | chr10 | 4847312 | |||||||
| chr10:4847333 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(110): Show |
278 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(275): Show |
intron_variant | MODIFIER | c.920+103T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 9/9 | chr10 | 4847333 | |||||||
| chr10:4847448 | T | C | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.921-40T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 9/9 | chr10 | 4847448 | |||||||
| chr10:4847470 | T | G | 17 | a0002c0002t0003g0008 a0002c0002t0003g0015 a0002c0002t0003g0016 others(14): Show |
29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.921-18T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 9/9 | chr10 | 4847470 |