Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1646 |
| ensemblid | ENSG00000151632.18 |
| hgncid | 385 |
| symbol | AKR1C2 |
| name | aldo-keto reductase family 1 member C2 |
| refseq_nuc | NM_001393392.1 |
| refseq_prot | NP_001380321.1 |
| ensembl_nuc | ENST00000380753.9 |
| ensembl_prot | ENSP00000370129.4 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 4987775 |
| end | 5003857 |
| strand | - |
| ver | v1.2 |
| region | chr10:4987775-5003857 |
| region5000 | chr10:4982775-5008857 |
| regionname0 | AKR1C2_chr10_4987775_5003857 |
| regionname5000 | AKR1C2_chr10_4982775_5008857 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 323 | 387 | 76 | 68 | 180 | 16 | 45 | 136 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | MDSKY others(318): Show |
chr10 | 4982775 | 5008857 |
| a0002 | 0/0 | 323 | 16 | 13 | 3 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | MDSKY others(318): Show |
chr10 | 4982775 | 5008857 |
| a0003 | 0/0 | 323 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | MDSKY others(318): Show |
chr10 | 4982775 | 5008857 |
| a0004 | 0/0 | 323 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | MDSKY others(318): Show |
chr10 | 4982775 | 5008857 |
| a0005 | 0/0 | 323 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | MDSKY others(318): Show |
chr10 | 4982775 | 5008857 |
| a0006 | 0/0 | 323 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | MDSKY others(318): Show |
chr10 | 4982775 | 5008857 |
| a0007 | 0/0 | 323 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | MDSKY others(318): Show |
chr10 | 4982775 | 5008857 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 969 | 313 | 46 | 50 | 173 | 9 | 33 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | ATGGA others(964): Show |
chr10 | 4982775 | 5008857 | ||
| a0001c0002 | 0/0 | 969 | 36 | 14 | 5 | 4 | 4 | 9 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | ATGGA others(964): Show |
chr10 | 4982775 | 5008857 | ||
| a0001c0003 | 0/0 | 969 | 19 | 3 | 10 | 0 | 3 | 3 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | ATGGA others(964): Show |
chr10 | 4982775 | 5008857 | ||
| a0001c0005 | 0/0 | 969 | 11 | 11 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | ATGGA others(964): Show |
chr10 | 4982775 | 5008857 | ||
| a0001c0007 | 0/0 | 969 | 3 | 0 | 3 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | ATGGA others(964): Show |
chr10 | 4982775 | 5008857 | ||
| a0001c0008 | 0/0 | 969 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | ATGGA others(964): Show |
chr10 | 4982775 | 5008857 | ||
| a0001c0012 | 0/0 | 969 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | ATGGA others(964): Show |
chr10 | 4982775 | 5008857 | ||
| a0001c0013 | 0/0 | 969 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | ATGGA others(964): Show |
chr10 | 4982775 | 5008857 | ||
| a0001c0015 | 0/0 | 969 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | ATGGA others(964): Show |
chr10 | 4982775 | 5008857 | ||
| a0002c0004 | 0/0 | 969 | 16 | 13 | 3 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | ATGGA others(964): Show |
chr10 | 4982775 | 5008857 | ||
| a0003c0006 | 0/0 | 969 | 3 | 0 | 2 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | ATGGA others(964): Show |
chr10 | 4982775 | 5008857 | ||
| a0004c0010 | 0/0 | 969 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | ATGGA others(964): Show |
chr10 | 4982775 | 5008857 | ||
| a0004c0011 | 0/0 | 969 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | ATGGA others(964): Show |
chr10 | 4982775 | 5008857 | ||
| a0005c0009 | 0/0 | 969 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | ATGGA others(964): Show |
chr10 | 4982775 | 5008857 | ||
| a0006c0016 | 0/0 | 969 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | ATGGA others(964): Show |
chr10 | 4982775 | 5008857 | ||
| a0007c0014 | 0/0 | 969 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | ATGGA others(964): Show |
chr10 | 4982775 | 5008857 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3215 | 131 | 2 | 21 | 92 | 2 | 14 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0002 | 0/0 | 3216 | 74 | 4 | 6 | 56 | 4 | 4 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3211): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0003 | 0/1 | 3214 | 25 | 10 | 7 | 0 | 1 | 6 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3209): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0004 | 0/0 | 3215 | 22 | 3 | 6 | 4 | 2 | 7 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0007 | 0/0 | 3214 | 3 | 3 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3209): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0008 | 0/0 | 3215 | 11 | 10 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0011 | 0/0 | 3215 | 4 | 0 | 0 | 4 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0013 | 0/0 | 3216 | 4 | 0 | 0 | 4 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3211): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0014 | 0/0 | 3214 | 4 | 4 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3209): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0017 | 0/0 | 3215 | 3 | 0 | 0 | 3 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0018 | 1/0 | 3215 | 1 | 0 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0020 | 0/0 | 3215 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0021 | 0/0 | 3215 | 2 | 0 | 2 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0022 | 0/0 | 3215 | 2 | 1 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0023 | 0/0 | 3214 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3209): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0024 | 0/0 | 3215 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0028 | 0/0 | 3215 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0029 | 0/0 | 3215 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0033 | 0/0 | 3215 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0034 | 0/0 | 3216 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3211): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0035 | 0/0 | 3215 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0036 | 0/0 | 3215 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0037 | 0/0 | 3215 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0038 | 0/0 | 3216 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3211): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0039 | 0/0 | 3215 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0040 | 0/0 | 3214 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3209): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0041 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3209): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0042 | 0/0 | 3214 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3209): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0043 | 0/0 | 3216 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3211): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0044 | 0/0 | 3214 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3209): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0045 | 0/0 | 3215 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0046 | 0/0 | 3216 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3211): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0047 | 0/0 | 3216 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3211): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0048 | 0/0 | 3214 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3209): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0049 | 0/0 | 3216 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3211): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0050 | 0/0 | 3215 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0001t0051 | 0/0 | 3215 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0002t0005 | 0/0 | 3215 | 21 | 0 | 5 | 4 | 4 | 8 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0002t0006 | 0/0 | 3216 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3211): Show |
chr10 | 4982775 | 5008857 |
| a0001c0002t0012 | 0/0 | 3215 | 4 | 4 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0002t0015 | 0/0 | 3215 | 3 | 3 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0002t0016 | 0/0 | 3215 | 3 | 3 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0002t0030 | 0/0 | 3215 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0002t0031 | 0/0 | 3215 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0002t0032 | 0/0 | 3215 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0003t0007 | 0/0 | 3214 | 9 | 1 | 5 | 0 | 2 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3209): Show |
chr10 | 4982775 | 5008857 |
| a0001c0003t0009 | 0/0 | 3214 | 10 | 2 | 5 | 0 | 1 | 2 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3209): Show |
chr10 | 4982775 | 5008857 |
| a0001c0005t0007 | 0/0 | 3214 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3209): Show |
chr10 | 4982775 | 5008857 |
| a0001c0005t0010 | 0/0 | 3216 | 7 | 7 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3211): Show |
chr10 | 4982775 | 5008857 |
| a0001c0005t0025 | 0/0 | 3216 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3211): Show |
chr10 | 4982775 | 5008857 |
| a0001c0005t0027 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3209): Show |
chr10 | 4982775 | 5008857 |
| a0001c0007t0004 | 0/0 | 3215 | 3 | 0 | 3 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0008t0008 | 0/0 | 3215 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0012t0001 | 0/0 | 3215 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0013t0001 | 0/0 | 3215 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0001c0015t0005 | 0/0 | 3215 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0002c0004t0006 | 0/0 | 3216 | 13 | 12 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3211): Show |
chr10 | 4982775 | 5008857 |
| a0002c0004t0019 | 0/0 | 3216 | 2 | 0 | 2 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3211): Show |
chr10 | 4982775 | 5008857 |
| a0002c0004t0026 | 0/0 | 3216 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3211): Show |
chr10 | 4982775 | 5008857 |
| a0003c0006t0001 | 0/0 | 3215 | 3 | 0 | 2 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0004c0010t0003 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3209): Show |
chr10 | 4982775 | 5008857 |
| a0004c0011t0007 | 0/0 | 3214 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3209): Show |
chr10 | 4982775 | 5008857 |
| a0005c0009t0018 | 0/0 | 3215 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3210): Show |
chr10 | 4982775 | 5008857 |
| a0006c0016t0003 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3209): Show |
chr10 | 4982775 | 5008857 |
| a0007c0014t0010 | 0/0 | 3216 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | GCTAA others(3211): Show |
chr10 | 4982775 | 5008857 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 56 | 1 | 5 | 41 | 1 | 8 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0003 | 0/0 | 20 | 0 | 8 | 12 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0010 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0002g0002 | 0/0 | 52 | 3 | 4 | 39 | 3 | 3 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0002g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0003g0004 | 0/0 | 12 | 6 | 3 | 0 | 1 | 2 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0003g0020 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0003g0021 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0003g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0003g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0004g0007 | 0/0 | 9 | 0 | 4 | 1 | 1 | 3 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0004g0012 | 0/0 | 6 | 0 | 1 | 3 | 1 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0004g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0007g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0008g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0008g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0008g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0008g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0011g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0013g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0013g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0014g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0014g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0017g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0017g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0018g0094 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0020g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0021g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0022g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0023g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0024g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0028g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0029g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0033g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0034g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0035g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0036g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0037g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0038g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0039g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0040g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0041g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0042g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0043g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0044g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0045g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0046g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0047g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0048g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0049g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0050g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0001t0051g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0002t0005g0005 | 0/0 | 12 | 0 | 4 | 0 | 4 | 4 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0002t0005g0051 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0002t0005g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0002t0005g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0002t0005g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0002t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0002t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0002t0005g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0002t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0002t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0002t0012g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0002t0015g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0002t0016g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0002t0030g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0002t0031g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0002t0032g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0003t0007g0011 | 0/0 | 6 | 1 | 4 | 0 | 1 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0003t0007g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0003t0007g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0003t0009g0013 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0003t0009g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0003t0009g0039 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0003t0009g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0005t0007g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0005t0010g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0005t0010g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0005t0010g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0005t0025g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0005t0027g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0007t0004g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0008t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0008t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0012t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0013t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0001c0015t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0002c0004t0006g0006 | 0/0 | 11 | 10 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0002c0004t0006g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0002c0004t0019g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0002c0004t0026g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0003c0006t0001g0024 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0004c0010t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0004c0011t0007g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0005c0009t0018g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0006c0016t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| a0007c0014t0010g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | GBR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00140 | hp1 | a0001 | c0003 | t0007 | g0037 | EUR | GBR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00140 | hp2 | a0001 | c0002 | t0005 | g0005 | EUR | GBR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0007 | EUR | FIN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00280 | hp2 | a0001 | c0003 | t0007 | g0011 | EUR | FIN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0012 | EUR | FIN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00323 | hp2 | a0001 | c0003 | t0009 | g0091 | EUR | FIN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00408 | hp2 | a0001 | c0001 | t0024 | g0049 | EAS | CHS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00558 | hp2 | a0001 | c0001 | t0033 | g0109 | EAS | CHS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | CHS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00609 | hp1 | a0001 | c0013 | t0001 | g0122 | EAS | CHS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00642 | hp2 | a0001 | c0003 | t0007 | g0011 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00735 | hp1 | a0001 | c0001 | t0043 | g0061 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00738 | hp1 | a0001 | c0003 | t0007 | g0011 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01070 | hp1 | a0001 | c0007 | t0004 | g0023 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01070 | hp2 | a0001 | c0003 | t0007 | g0037 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01071 | hp1 | a0001 | c0007 | t0004 | g0023 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01074 | hp1 | a0001 | c0007 | t0004 | g0023 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01081 | hp2 | a0001 | c0001 | t0042 | g0087 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0086 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01099 | hp2 | a0001 | c0002 | t0005 | g0005 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01106 | hp2 | a0001 | c0003 | t0007 | g0011 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01109 | hp1 | a0001 | c0001 | t0045 | g0089 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01109 | hp2 | a0002 | c0004 | t0019 | g0033 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01167 | hp1 | a0001 | c0003 | t0009 | g0038 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01168 | hp1 | a0003 | c0006 | t0001 | g0024 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01168 | hp2 | a0001 | c0003 | t0007 | g0011 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01169 | hp1 | a0001 | c0003 | t0009 | g0038 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01169 | hp2 | a0003 | c0006 | t0001 | g0024 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01175 | hp2 | a0002 | c0004 | t0019 | g0033 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01192 | hp2 | a0001 | c0002 | t0005 | g0005 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01243 | hp1 | a0001 | c0001 | t0022 | g0035 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01243 | hp2 | a0002 | c0004 | t0006 | g0006 | AMR | PUR | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01255 | hp1 | a0004 | c0011 | t0007 | g0148 | AMR | CLM | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | CLM | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01261 | hp1 | a0001 | c0002 | t0005 | g0005 | AMR | CLM | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01261 | hp2 | a0001 | c0003 | t0009 | g0013 | AMR | CLM | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01346 | hp1 | a0001 | c0001 | t0021 | g0047 | AMR | CLM | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01361 | hp1 | a0001 | c0003 | t0009 | g0013 | AMR | CLM | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01433 | hp1 | a0001 | c0002 | t0005 | g0005 | AMR | CLM | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01515 | hp1 | a0001 | c0002 | t0005 | g0005 | EUR | IBS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | IBS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01516 | hp1 | a0001 | c0002 | t0005 | g0005 | EUR | IBS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0009 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0043 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01891 | hp2 | a0001 | c0001 | t0014 | g0073 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01928 | hp1 | a0001 | c0001 | t0039 | g0097 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01975 | hp2 | a0001 | c0001 | t0034 | g0130 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01978 | hp1 | a0001 | c0001 | t0029 | g0123 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02027 | hp1 | a0001 | c0001 | t0024 | g0049 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02055 | hp2 | a0001 | c0005 | t0027 | g0101 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02080 | hp1 | a0001 | c0001 | t0037 | g0133 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02129 | hp2 | a0001 | c0001 | t0036 | g0132 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02132 | hp2 | a0001 | c0015 | t0005 | g0155 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02145 | hp2 | a0001 | c0005 | t0010 | g0017 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02257 | hp2 | a0001 | c0002 | t0015 | g0026 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02258 | hp2 | a0001 | c0005 | t0010 | g0018 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02280 | hp1 | a0001 | c0005 | t0010 | g0017 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0096 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02293 | hp1 | a0001 | c0001 | t0040 | g0075 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02300 | hp2 | a0001 | c0002 | t0005 | g0051 | AMR | PEL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02572 | hp1 | a0001 | c0002 | t0015 | g0026 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02602 | hp1 | a0001 | c0003 | t0007 | g0090 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02615 | hp1 | a0001 | c0001 | t0014 | g0022 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02615 | hp2 | a0001 | c0001 | t0023 | g0034 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02622 | hp2 | a0002 | c0004 | t0006 | g0032 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02630 | hp1 | a0001 | c0001 | t0014 | g0022 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02630 | hp2 | a0002 | c0004 | t0006 | g0006 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02647 | hp2 | a0001 | c0001 | t0023 | g0034 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02698 | hp1 | a0001 | c0002 | t0005 | g0051 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02717 | hp1 | a0001 | c0001 | t0014 | g0022 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02717 | hp2 | a0001 | c0002 | t0016 | g0027 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0043 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0045 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02809 | hp1 | a0001 | c0002 | t0012 | g0016 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02809 | hp2 | a0001 | c0003 | t0007 | g0011 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02818 | hp1 | a0001 | c0001 | t0020 | g0036 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02886 | hp1 | a0001 | c0002 | t0015 | g0026 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02886 | hp2 | a0002 | c0004 | t0006 | g0032 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02896 | hp2 | a0001 | c0002 | t0016 | g0027 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02897 | hp1 | a0002 | c0004 | t0026 | g0080 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02897 | hp2 | a0001 | c0002 | t0016 | g0027 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02922 | hp1 | a0006 | c0016 | t0003 | g0079 | AFR | ESN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02922 | hp2 | a0001 | c0001 | t0022 | g0035 | AFR | ESN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02965 | hp1 | a0002 | c0004 | t0006 | g0006 | AFR | ESN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02965 | hp2 | a0001 | c0005 | t0010 | g0017 | AFR | ESN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | ESN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02970 | hp2 | a0001 | c0008 | t0008 | g0053 | AFR | ESN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | ESN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02976 | hp2 | a0005 | c0009 | t0018 | g0040 | AFR | ESN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03041 | hp1 | a0002 | c0004 | t0006 | g0006 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03041 | hp2 | a0001 | c0002 | t0032 | g0150 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03098 | hp1 | a0002 | c0004 | t0006 | g0006 | AFR | MSL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03098 | hp2 | a0001 | c0002 | t0006 | g0152 | AFR | MSL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03130 | hp1 | a0001 | c0005 | t0010 | g0018 | AFR | ESN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03130 | hp2 | a0001 | c0008 | t0008 | g0054 | AFR | ESN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03139 | hp1 | a0004 | c0010 | t0003 | g0147 | AFR | ESN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03139 | hp2 | a0001 | c0002 | t0012 | g0016 | AFR | ESN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0045 | AFR | ESN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03195 | hp2 | a0002 | c0004 | t0006 | g0006 | AFR | ESN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03209 | hp2 | a0001 | c0005 | t0007 | g0042 | AFR | MSL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03225 | hp1 | a0001 | c0002 | t0012 | g0016 | AFR | MSL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | MSL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03239 | hp1 | a0001 | c0002 | t0005 | g0005 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0041 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0020 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03491 | hp2 | a0001 | c0002 | t0005 | g0158 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0041 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03516 | hp1 | a0001 | c0002 | t0012 | g0016 | AFR | ESN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0105 | AFR | ESN | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03540 | hp1 | a0001 | c0001 | t0041 | g0076 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03540 | hp2 | a0002 | c0004 | t0006 | g0006 | AFR | GWD | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03579 | hp1 | a0001 | c0001 | t0050 | g0093 | AFR | MSL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03579 | hp2 | a0001 | c0002 | t0031 | g0149 | AFR | MSL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03654 | hp1 | a0001 | c0002 | t0005 | g0154 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03669 | hp2 | a0001 | c0003 | t0009 | g0013 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | STU | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03704 | hp1 | a0001 | c0002 | t0030 | g0153 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03704 | hp2 | a0001 | c0002 | t0005 | g0005 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0012 | SAS | BEB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0098 | SAS | BEB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03927 | hp2 | a0003 | c0006 | t0001 | g0024 | SAS | BEB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0072 | SAS | STU | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG04115 | hp2 | a0001 | c0003 | t0009 | g0039 | SAS | STU | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG04184 | hp1 | a0001 | c0001 | t0048 | g0099 | SAS | BEB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG04199 | hp1 | a0001 | c0002 | t0005 | g0005 | SAS | STU | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG04199 | hp2 | a0001 | c0001 | t0044 | g0071 | SAS | STU | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG04204 | hp2 | a0001 | c0002 | t0005 | g0005 | SAS | STU | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG04228 | hp2 | a0001 | c0002 | t0005 | g0146 | SAS | STU | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18522 | hp1 | a0001 | c0001 | t0020 | g0036 | AFR | YRI | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | YRI | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18612 | hp2 | a0001 | c0002 | t0005 | g0157 | EAS | CHB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18747 | hp1 | a0001 | c0001 | t0017 | g0028 | EAS | CHB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | YRI | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18906 | hp2 | a0007 | c0014 | t0010 | g0144 | AFR | YRI | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18942 | hp1 | a0001 | c0001 | t0013 | g0019 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18952 | hp1 | a0001 | c0001 | t0011 | g0015 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18957 | hp1 | a0001 | c0001 | t0017 | g0028 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18970 | hp2 | a0001 | c0001 | t0013 | g0068 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18971 | hp2 | a0001 | c0002 | t0005 | g0052 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18972 | hp1 | a0001 | c0001 | t0008 | g0084 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18989 | hp1 | a0001 | c0001 | t0046 | g0057 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18993 | hp2 | a0001 | c0001 | t0013 | g0019 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18995 | hp2 | a0001 | c0001 | t0011 | g0015 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18998 | hp2 | a0001 | c0001 | t0038 | g0124 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19000 | hp1 | a0001 | c0001 | t0035 | g0131 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19005 | hp2 | a0001 | c0001 | t0013 | g0019 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19012 | hp2 | a0001 | c0001 | t0011 | g0015 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | LWK | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19030 | hp2 | a0001 | c0005 | t0010 | g0143 | AFR | LWK | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19043 | hp1 | a0001 | c0001 | t0028 | g0092 | AFR | LWK | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19043 | hp2 | a0001 | c0001 | t0049 | g0058 | AFR | LWK | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19059 | hp1 | a0001 | c0002 | t0005 | g0156 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19059 | hp2 | a0001 | c0001 | t0017 | g0065 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19070 | hp2 | a0001 | c0001 | t0011 | g0015 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19082 | hp2 | a0001 | c0002 | t0005 | g0052 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19085 | hp1 | a0001 | c0012 | t0001 | g0119 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19088 | hp1 | a0001 | c0001 | t0051 | g0134 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19240 | hp1 | a0002 | c0004 | t0006 | g0006 | AFR | YRI | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | YRI | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA20129 | hp1 | a0001 | c0005 | t0007 | g0042 | AFR | ASW | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA20129 | hp2 | a0002 | c0004 | t0006 | g0006 | AFR | ASW | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0062 | EUR | TSI | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA20805 | hp2 | a0001 | c0002 | t0005 | g0005 | EUR | TSI | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | GIH | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | GIH | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01123 | hp1 | a0001 | c0003 | t0009 | g0013 | AMR | CLM | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG01123 | hp2 | a0001 | c0001 | t0021 | g0047 | AMR | CLM | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02109 | hp2 | a0002 | c0004 | t0006 | g0006 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0095 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02486 | hp2 | a0002 | c0004 | t0006 | g0006 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0088 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG02559 | hp2 | a0005 | c0009 | t0018 | g0040 | AFR | ACB | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03471 | hp1 | a0001 | c0005 | t0025 | g0056 | AFR | MSL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG03471 | hp2 | a0001 | c0002 | t0006 | g0151 | AFR | MSL | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0100 | AFR | USA | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| HG06807 | hp2 | a0001 | c0005 | t0010 | g0018 | AFR | USA | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA20300 | hp1 | a0001 | c0003 | t0009 | g0039 | AFR | USA | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA21309 | hp1 | a0001 | c0001 | t0047 | g0106 | AFR | LWK | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| NA21309 | hp2 | a0001 | c0003 | t0009 | g0013 | AFR | LWK | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0070 | REF | REF | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0018 | g0094 | REF | REF | AKR1C2_chr10_4982775_5008857 | AKR1C2 | chr10 | 4982775 | 5008857 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:4995328 | C | G | 1 | a0005 | 2 | HG02559.hp2 HG02976.hp2 |
missense_variant | MODERATE | c.837G>C | p.Gln279His | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/9 | 859/3215 | 837/972 | 279/323 | chr10 | 4995328 | |||
| chr10:4999225 | G | C | 1 | a0007 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.422C>G | p.Thr141Arg | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 4/9 | 444/3215 | 422/972 | 141/323 | chr10 | 4999225 | |||
| chr10:5000555 | C | T | 1 | a0004 | 2 | HG01255.hp1 HG03139.hp1 |
missense_variant | MODERATE | c.364G>A | p.Val122Ile | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/9 | 386/3215 | 364/972 | 122/323 | chr10 | 5000555 | |||
| chr10:5001555 | C | G | 1 | a0003 | 3 | HG01168.hp1 HG01169.hp2 HG03927.hp2 |
missense_variant | MODERATE | c.211G>C | p.Asp71His | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 2/9 | 233/3215 | 211/972 | 71/323 | chr10 | 5001555 | |||
| chr10:5001557 | G | A | 1 | a0006 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.209C>T | p.Ala70Val | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 2/9 | 231/3215 | 209/972 | 70/323 | chr10 | 5001557 | |||
| chr10:5001629 | A | T | 1 | a0002 | 16 | HG01109.hp2 HG01175.hp2 HG01243.hp2 others(13): Show |
missense_variant | MODERATE | c.137T>A | p.Phe46Tyr | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 2/9 | 159/3215 | 137/972 | 46/323 | chr10 | 5001629 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:4995382 | C | T | 2 | a0001c0012 a0001c0013 |
2 | HG00609.hp1 NA19085.hp1 |
synonymous_variant | LOW | c.783G>A | p.Leu261Leu | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/9 | 805/3215 | 783/972 | 261/323 | chr10 | 4995382 | |||
| chr10:4995770 | A | G | 4 | a0001c0005 a0001c0012 a0001c0015 others(1): Show |
14 | HG02055.hp2 HG02132.hp2 HG02145.hp2 others(11): Show |
synonymous_variant | LOW | c.666T>C | p.His222His | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 6/9 | 688/3215 | 666/972 | 222/323 | chr10 | 4995770 | |||
| chr10:4999206 | T | C | 1 | a0001c0003 | 19 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(16): Show |
synonymous_variant | LOW | c.441A>G | p.Thr147Thr | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 4/9 | 463/3215 | 441/972 | 147/323 | chr10 | 4999206 | |||
| chr10:5000577 | A | G | 1 | a0004c0010 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.342T>C | p.Tyr114Tyr | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/9 | 364/3215 | 342/972 | 114/323 | chr10 | 5000577 | |||
| chr10:5000592 | G | A | 2 | a0001c0002 a0001c0015 |
37 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(34): Show |
synonymous_variant | LOW | c.327C>T | p.Asp109Asp | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/9 | 349/3215 | 327/972 | 109/323 | chr10 | 5000592 | |||
| chr10:5000597 | A | G | 1 | a0001c0007 | 3 | HG01070.hp1 HG01071.hp1 HG01074.hp1 |
synonymous_variant | LOW | c.322T>C | p.Leu108Leu | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/9 | 344/3215 | 322/972 | 108/323 | chr10 | 5000597 | |||
| chr10:5003761 | C | T | 1 | a0001c0008 | 2 | HG02970.hp2 HG03130.hp2 |
synonymous_variant | LOW | c.75G>A | p.Ala25Ala | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/9 | 97/3215 | 75/972 | 25/323 | chr10 | 5003761 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:4987848 | G | A | 8 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0017 others(5): Show |
86 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*2148C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 2148 | chr10 | 4987848 | ||||||
| chr10:4987874 | C | A | 1 | a0001c0001t0035 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2122G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 2122 | chr10 | 4987874 | ||||||
| chr10:4987956 | T | C | 4 | a0001c0001t0004 a0001c0001t0039 a0001c0001t0048 others(1): Show |
27 | HG00280.hp1 HG00323.hp1 HG01070.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2040A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 2040 | chr10 | 4987956 | ||||||
| chr10:4987962 | G | C | 1 | a0001c0001t0039 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2034C>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 2034 | chr10 | 4987962 | ||||||
| chr10:4988004 | A | G | 1 | a0001c0001t0046 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1992T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1992 | chr10 | 4988004 | ||||||
| chr10:4988006 | C | CT | 15 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0034 others(12): Show |
111 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*1989dupA | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1989 | chr10 | 4988006 | ||||||
| chr10:4988075 | C | T | 9 | a0001c0001t0020 a0001c0002t0005 a0001c0002t0012 others(6): Show |
37 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1921G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1921 | chr10 | 4988075 | ||||||
| chr10:4988135 | G | T | 1 | a0001c0001t0011 | 4 | NA18952.hp1 NA18995.hp2 NA19012.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1861C>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1861 | chr10 | 4988135 | ||||||
| chr10:4988163 | C | T | 2 | a0001c0001t0045 a0002c0004t0019 |
3 | HG01109.hp1 HG01109.hp2 HG01175.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1833G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1833 | chr10 | 4988163 | ||||||
| chr10:4988173 | G | A | 1 | a0001c0001t0036 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1823C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1823 | chr10 | 4988173 | ||||||
| chr10:4988176 | A | T | 8 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0040 others(5): Show |
34 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1820T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1820 | chr10 | 4988176 | ||||||
| chr10:4988258 | T | C | 1 | a0001c0001t0022 | 2 | HG01243.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1738A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1738 | chr10 | 4988258 | ||||||
| chr10:4988287 | G | C | 1 | a0001c0003t0009 | 10 | HG00323.hp2 HG01123.hp1 HG01167.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1709C>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1709 | chr10 | 4988287 | ||||||
| chr10:4988334 | G | A | 9 | a0001c0001t0020 a0001c0002t0005 a0001c0002t0012 others(6): Show |
37 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1662C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1662 | chr10 | 4988334 | ||||||
| chr10:4988341 | T | C | 6 | a0001c0002t0005 a0001c0002t0012 a0001c0002t0015 others(3): Show |
33 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1655A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1655 | chr10 | 4988341 | ||||||
| chr10:4988350 | A | G | 1 | a0001c0001t0014 | 4 | HG01891.hp2 HG02615.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1646T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1646 | chr10 | 4988350 | ||||||
| chr10:4988426 | AT | A | 19 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(16): Show |
89 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*1569delA | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1569 | chr10 | 4988426 | ||||||
| chr10:4988555 | C | A | 1 | a0001c0002t0032 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1441G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1441 | chr10 | 4988555 | ||||||
| chr10:4988556 | T | C | 1 | a0001c0002t0032 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1440A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1440 | chr10 | 4988556 | ||||||
| chr10:4988644 | G | A | 1 | a0001c0001t0037 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1352C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1352 | chr10 | 4988644 | ||||||
| chr10:4988668 | A | G | 9 | a0001c0001t0020 a0001c0002t0005 a0001c0002t0012 others(6): Show |
37 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1328T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1328 | chr10 | 4988668 | ||||||
| chr10:4988711 | A | C | 8 | a0001c0002t0005 a0001c0002t0012 a0001c0002t0015 others(5): Show |
35 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1285T>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1285 | chr10 | 4988711 | ||||||
| chr10:4988714 | G | A | 8 | a0001c0002t0005 a0001c0002t0012 a0001c0002t0015 others(5): Show |
35 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1282C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1282 | chr10 | 4988714 | ||||||
| chr10:4988724 | A | T | 8 | a0001c0002t0005 a0001c0002t0012 a0001c0002t0015 others(5): Show |
35 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1272T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1272 | chr10 | 4988724 | ||||||
| chr10:4988764 | A | G | 16 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0040 others(13): Show |
69 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1232T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1232 | chr10 | 4988764 | ||||||
| chr10:4988788 | A | G | 1 | a0001c0002t0016 | 3 | HG02717.hp2 HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1208T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1208 | chr10 | 4988788 | ||||||
| chr10:4988804 | C | T | 1 | a0001c0001t0044 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1192G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1192 | chr10 | 4988804 | ||||||
| chr10:4988805 | G | T | 1 | a0001c0001t0033 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1191C>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1191 | chr10 | 4988805 | ||||||
| chr10:4988834 | T | A | 9 | a0001c0001t0020 a0001c0002t0005 a0001c0002t0012 others(6): Show |
37 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1162A>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1162 | chr10 | 4988834 | ||||||
| chr10:4988835 | G | A | 9 | a0001c0001t0020 a0001c0002t0005 a0001c0002t0012 others(6): Show |
37 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1161C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1161 | chr10 | 4988835 | ||||||
| chr10:4988836 | A | C | 9 | a0001c0001t0020 a0001c0002t0005 a0001c0002t0012 others(6): Show |
37 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1160T>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1160 | chr10 | 4988836 | ||||||
| chr10:4988841 | T | G | 9 | a0001c0001t0020 a0001c0002t0005 a0001c0002t0012 others(6): Show |
37 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1155A>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1155 | chr10 | 4988841 | ||||||
| chr10:4988852 | A | G | 1 | a0001c0001t0013 | 4 | NA18942.hp1 NA18970.hp2 NA18993.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1144T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1144 | chr10 | 4988852 | ||||||
| chr10:4988887 | C | G | 1 | a0001c0001t0043 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1109G>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1109 | chr10 | 4988887 | ||||||
| chr10:4988951 | A | C | 1 | a0001c0001t0042 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1045T>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 1045 | chr10 | 4988951 | ||||||
| chr10:4989038 | A | T | 2 | a0001c0001t0042 a0001c0001t0050 |
2 | HG01081.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*958T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 958 | chr10 | 4989038 | ||||||
| chr10:4989093 | C | A | 9 | a0001c0001t0020 a0001c0002t0005 a0001c0002t0012 others(6): Show |
37 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*903G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 903 | chr10 | 4989093 | ||||||
| chr10:4989119 | T | G | 1 | a0001c0001t0049 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*877A>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 877 | chr10 | 4989119 | ||||||
| chr10:4989121 | C | G | 2 | a0001c0001t0020 a0001c0002t0030 |
3 | HG02818.hp1 HG03704.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*875G>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 875 | chr10 | 4989121 | ||||||
| chr10:4989168 | G | T | 10 | a0001c0001t0020 a0001c0001t0041 a0001c0002t0005 others(7): Show |
38 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*828C>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 828 | chr10 | 4989168 | ||||||
| chr10:4989203 | A | T | 1 | a0001c0001t0040 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*793T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 793 | chr10 | 4989203 | ||||||
| chr10:4989387 | C | A | 1 | a0001c0001t0021 | 2 | HG01123.hp2 HG01346.hp1 |
3_prime_UTR_variant | MODIFIER | c.*609G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 609 | chr10 | 4989387 | ||||||
| chr10:4989436 | A | AC | 3 | a0001c0001t0004 a0001c0001t0039 a0001c0007t0004 |
26 | HG00280.hp1 HG00323.hp1 HG01070.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*559dupG | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 559 | chr10 | 4989436 | ||||||
| chr10:4989441 | C | A | 1 | a0001c0003t0009 | 10 | HG00323.hp2 HG01123.hp1 HG01167.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*555G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 555 | chr10 | 4989441 | ||||||
| chr10:4989442 | C | T | 1 | a0002c0004t0026 | 1 | HG02897.hp1 | 3_prime_UTR_variant | MODIFIER | c.*554G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 554 | chr10 | 4989442 | ||||||
| chr10:4989452 | A | T | 24 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0020 others(21): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*544T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 544 | chr10 | 4989452 | ||||||
| chr10:4989517 | A | G | 59 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(56): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
3_prime_UTR_variant | MODIFIER | c.*479T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 479 | chr10 | 4989517 | ||||||
| chr10:4989685 | C | T | 23 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0020 others(20): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*311G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 311 | chr10 | 4989685 | ||||||
| chr10:4989689 | G | A | 1 | a0001c0001t0028 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*307C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 307 | chr10 | 4989689 | ||||||
| chr10:4989699 | G | T | 3 | a0001c0005t0010 a0001c0005t0025 a0007c0014t0010 |
9 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*297C>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 297 | chr10 | 4989699 | ||||||
| chr10:4989719 | G | A | 1 | a0001c0001t0051 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*277C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 277 | chr10 | 4989719 | ||||||
| chr10:4989724 | C | T | 1 | a0001c0001t0029 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*272G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 272 | chr10 | 4989724 | ||||||
| chr10:4989768 | C | G | 2 | a0001c0001t0028 a0001c0005t0027 |
2 | HG02055.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*228G>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 228 | chr10 | 4989768 | ||||||
| chr10:4989823 | C | T | 4 | a0001c0002t0006 a0002c0004t0006 a0002c0004t0019 others(1): Show |
18 | HG01109.hp2 HG01175.hp2 HG01243.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*173G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 173 | chr10 | 4989823 | ||||||
| chr10:4989849 | C | T | 1 | a0001c0005t0025 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*147G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 147 | chr10 | 4989849 | ||||||
| chr10:4989884 | G | C | 1 | a0001c0001t0024 | 2 | HG00408.hp2 HG02027.hp1 |
3_prime_UTR_variant | MODIFIER | c.*112C>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 112 | chr10 | 4989884 | ||||||
| chr10:4989957 | G | T | 1 | a0001c0002t0015 | 3 | HG02257.hp2 HG02572.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*39C>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 9/9 | 39 | chr10 | 4989957 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:4990047 | A | AG | 55 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(52): Show |
153 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.930-10dupC | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990047 | |||||||
| chr10:4990092 | C | T | 16 | a0001c0001t0003g0004 a0001c0001t0003g0020 a0001c0001t0003g0021 others(13): Show |
34 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.930-54G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990092 | |||||||
| chr10:4990093 | C | G | 2 | a0001c0001t0004g0041 a0001c0001t0004g0100 |
3 | HG03490.hp1 HG03492.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.930-55G>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990093 | |||||||
| chr10:4990094 | C | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(70): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.930-56G>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990094 | |||||||
| chr10:4990099 | C | T | 2 | a0001c0001t0004g0041 a0001c0001t0004g0100 |
3 | HG03490.hp1 HG03492.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.930-61G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990099 | |||||||
| chr10:4990122 | C | T | 1 | a0001c0001t0004g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.930-84G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990122 | |||||||
| chr10:4990191 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0135 |
2 | HG00099.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.930-153C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990191 | |||||||
| chr10:4990202 | A | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | NA18948.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.930-164T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990202 | |||||||
| chr10:4990242 | C | A | 45 | a0001c0001t0003g0004 a0001c0001t0003g0020 a0001c0001t0003g0021 others(42): Show |
100 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.930-204G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990242 | |||||||
| chr10:4990319 | A | T | 1 | a0004c0011t0007g0148 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.930-281T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990319 | |||||||
| chr10:4990351 | C | T | 1 | a0001c0001t0043g0061 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.930-313G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990351 | |||||||
| chr10:4990371 | C | T | 1 | a0001c0001t0042g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.930-333G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990371 | |||||||
| chr10:4990509 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(53): Show |
154 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.930-471T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990509 | |||||||
| chr10:4990512 | A | G | 15 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(12): Show |
35 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.930-474T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990512 | |||||||
| chr10:4990657 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.930-619G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990657 | |||||||
| chr10:4990721 | G | A | 16 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(13): Show |
36 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.930-683C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990721 | |||||||
| chr10:4990824 | C | G | 13 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(10): Show |
33 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.930-786G>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990824 | |||||||
| chr10:4990824 | C | T | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.930-786G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990824 | |||||||
| chr10:4990825 | A | G | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.930-787T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990825 | |||||||
| chr10:4990829 | G | T | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.930-791C>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990829 | |||||||
| chr10:4990834 | C | A | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.930-796G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990834 | |||||||
| chr10:4990835 | A | C | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.930-797T>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990835 | |||||||
| chr10:4990866 | A | T | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.930-828T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990866 | |||||||
| chr10:4990874 | T | C | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.930-836A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990874 | |||||||
| chr10:4990878 | A | G | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.930-840T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990878 | |||||||
| chr10:4990897 | T | C | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.930-859A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990897 | |||||||
| chr10:4990898 | G | T | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.930-860C>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990898 | |||||||
| chr10:4990903 | G | A | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.930-865C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990903 | |||||||
| chr10:4990906 | G | A | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.930-868C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990906 | |||||||
| chr10:4990963 | G | T | 5 | a0001c0005t0010g0017 a0001c0005t0010g0018 a0001c0005t0010g0143 others(2): Show |
9 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.929+868C>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4990963 | |||||||
| chr10:4991007 | A | G | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.929+824T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991007 | |||||||
| chr10:4991013 | T | C | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.929+818A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991013 | |||||||
| chr10:4991015 | C | T | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.929+816G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991015 | |||||||
| chr10:4991022 | A | G | 1 | a0001c0001t0003g0074 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.929+809T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991022 | |||||||
| chr10:4991023 | T | G | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.929+808A>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991023 | |||||||
| chr10:4991038 | C | CT | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.929+792dupA | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991038 | |||||||
| chr10:4991040 | T | C | 16 | a0001c0001t0003g0004 a0001c0001t0003g0020 a0001c0001t0003g0021 others(13): Show |
34 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.929+791A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991040 | |||||||
| chr10:4991053 | T | C | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.929+778A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991053 | |||||||
| chr10:4991054 | T | A | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.929+777A>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991054 | |||||||
| chr10:4991089 | T | C | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.929+742A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991089 | |||||||
| chr10:4991091 | T | C | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.929+740A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991091 | |||||||
| chr10:4991107 | G | T | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.929+724C>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991107 | |||||||
| chr10:4991111 | G | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(69): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.929+720C>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991111 | |||||||
| chr10:4991115 | C | T | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.929+716G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991115 | |||||||
| chr10:4991136 | T | C | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.929+695A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991136 | |||||||
| chr10:4991178 | C | T | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.929+653G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991178 | |||||||
| chr10:4991182 | C | T | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.929+649G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991182 | |||||||
| chr10:4991192 | A | G | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.929+639T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991192 | |||||||
| chr10:4991278 | A | G | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.929+553T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991278 | |||||||
| chr10:4991306 | A | C | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.929+525T>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991306 | |||||||
| chr10:4991313 | G | A | 1 | a0001c0001t0023g0034 | 2 | HG02615.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.929+518C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991313 | |||||||
| chr10:4991346 | T | C | 2 | a0001c0005t0010g0143 a0007c0014t0010g0144 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.929+485A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991346 | |||||||
| chr10:4991383 | G | A | 2 | a0001c0001t0008g0045 a0001c0001t0008g0105 |
3 | HG02723.hp2 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.929+448C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991383 | |||||||
| chr10:4991470 | A | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(141): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.929+361T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991470 | |||||||
| chr10:4991505 | C | A | 2 | a0001c0001t0008g0045 a0001c0001t0008g0105 |
3 | HG02723.hp2 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.929+326G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991505 | |||||||
| chr10:4991520 | T | A | 1 | a0001c0001t0002g0062 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.929+311A>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991520 | |||||||
| chr10:4991542 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.929+289C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991542 | |||||||
| chr10:4991645 | C | A | 29 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0029 others(26): Show |
103 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.929+186G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991645 | |||||||
| chr10:4991646 | A | G | 31 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0029 others(28): Show |
105 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.929+185T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991646 | |||||||
| chr10:4991752 | T | C | 7 | a0001c0001t0003g0077 a0001c0001t0008g0009 a0001c0001t0008g0045 others(4): Show |
14 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.929+79A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991752 | |||||||
| chr10:4991788 | C | T | 1 | a0001c0001t0007g0043 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.929+43G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991788 | |||||||
| chr10:4991810 | A | T | 1 | a0001c0001t0003g0078 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.929+21T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991810 | |||||||
| chr10:4991824 | T | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(55): Show |
156 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(153): Show |
splice_region_variant&intron_variant | LOW | c.929+7A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 8/8 | chr10 | 4991824 | |||||||
| chr10:4991964 | A | G | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.847-51T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4991964 | |||||||
| chr10:4992025 | C | T | 3 | a0001c0003t0007g0011 a0001c0003t0007g0037 a0001c0003t0007g0090 |
9 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.847-112G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992025 | |||||||
| chr10:4992067 | G | A | 1 | a0001c0001t0045g0089 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.847-154C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992067 | |||||||
| chr10:4992153 | A | G | 13 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(10): Show |
33 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.847-240T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992153 | |||||||
| chr10:4992181 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.847-268T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992181 | |||||||
| chr10:4992190 | T | C | 5 | a0001c0005t0010g0017 a0001c0005t0010g0018 a0001c0005t0010g0143 others(2): Show |
9 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.847-277A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992190 | |||||||
| chr10:4992208 | C | T | 15 | a0001c0001t0043g0061 a0001c0001t0045g0089 a0001c0002t0005g0005 others(12): Show |
35 | HG00140.hp2 HG00735.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.847-295G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992208 | |||||||
| chr10:4992375 | C | T | 4 | a0001c0001t0008g0009 a0001c0001t0047g0106 a0001c0008t0008g0053 others(1): Show |
10 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.847-462G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992375 | |||||||
| chr10:4992434 | C | A | 15 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(12): Show |
35 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.847-521G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992434 | |||||||
| chr10:4992485 | C | T | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.847-572G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992485 | |||||||
| chr10:4992568 | T | C | 24 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0029 others(21): Show |
86 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.847-655A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992568 | |||||||
| chr10:4992591 | T | G | 5 | a0001c0001t0004g0012 a0001c0001t0004g0086 a0001c0001t0004g0098 others(2): Show |
12 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.847-678A>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992591 | |||||||
| chr10:4992634 | AAAAGTTA others(69): Show |
A | 5 | a0001c0005t0010g0017 a0001c0005t0010g0018 a0001c0005t0010g0143 others(2): Show |
9 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.847-797_847-722del others(76): Show |
AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992634 | |||||||
| chr10:4992641 | A | G | 6 | a0001c0002t0006g0151 a0001c0002t0006g0152 a0002c0004t0006g0006 others(3): Show |
18 | HG01109.hp2 HG01175.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.847-728T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992641 | |||||||
| chr10:4992660 | A | T | 40 | a0001c0001t0003g0004 a0001c0001t0003g0020 a0001c0001t0003g0021 others(37): Show |
89 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.847-747T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992660 | |||||||
| chr10:4992680 | T | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(91): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.847-767A>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992680 | |||||||
| chr10:4992711 | G | T | 5 | a0001c0005t0010g0017 a0001c0005t0010g0018 a0001c0005t0010g0143 others(2): Show |
9 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.847-798C>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992711 | |||||||
| chr10:4992712 | A | C | 1 | a0001c0002t0005g0156 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.847-799T>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992712 | |||||||
| chr10:4992823 | G | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(67): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.847-910C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992823 | |||||||
| chr10:4992826 | A | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(67): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.847-913T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992826 | |||||||
| chr10:4992899 | G | A | 2 | a0001c0001t0008g0045 a0001c0001t0008g0105 |
3 | HG02723.hp2 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.847-986C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992899 | |||||||
| chr10:4992914 | C | T | 13 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(10): Show |
33 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.847-1001G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992914 | |||||||
| chr10:4992984 | C | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(67): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.847-1071G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4992984 | |||||||
| chr10:4993032 | A | C | 1 | a0001c0001t0001g0014 | 5 | HG00621.hp1 HG02074.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.847-1119T>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993032 | |||||||
| chr10:4993050 | T | C | 1 | a0001c0001t0022g0035 | 2 | HG01243.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.847-1137A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993050 | |||||||
| chr10:4993054 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(67): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.847-1141G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993054 | |||||||
| chr10:4993071 | G | C | 24 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0029 others(21): Show |
86 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.847-1158C>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993071 | |||||||
| chr10:4993088 | C | G | 1 | a0001c0001t0001g0126 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.847-1175G>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993088 | |||||||
| chr10:4993111 | T | C | 1 | a0001c0002t0005g0154 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.847-1198A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993111 | |||||||
| chr10:4993122 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.847-1209T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993122 | |||||||
| chr10:4993202 | G | A | 34 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0029 others(31): Show |
112 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.847-1289C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993202 | |||||||
| chr10:4993275 | A | T | 46 | a0001c0001t0003g0004 a0001c0001t0003g0020 a0001c0001t0003g0021 others(43): Show |
102 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.847-1362T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993275 | |||||||
| chr10:4993485 | T | A | 40 | a0001c0001t0003g0004 a0001c0001t0003g0020 a0001c0001t0003g0021 others(37): Show |
89 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.847-1572A>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993485 | |||||||
| chr10:4993486 | A | T | 40 | a0001c0001t0003g0004 a0001c0001t0003g0020 a0001c0001t0003g0021 others(37): Show |
89 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.847-1573T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993486 | |||||||
| chr10:4993620 | T | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0136 |
2 | HG01192.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.846+1699A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993620 | |||||||
| chr10:4993634 | G | A | 1 | a0004c0011t0007g0148 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.846+1685C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993634 | |||||||
| chr10:4993637 | T | C | 1 | a0001c0001t0024g0049 | 2 | HG00408.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.846+1682A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993637 | |||||||
| chr10:4993675 | A | G | 1 | a0001c0001t0014g0073 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.846+1644T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993675 | |||||||
| chr10:4993678 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(53): Show |
154 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.846+1641T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993678 | |||||||
| chr10:4993725 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.846+1594C>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993725 | |||||||
| chr10:4993739 | C | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(149): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.846+1580G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993739 | |||||||
| chr10:4993805 | CAT | C | 2 | a0001c0001t0007g0088 a0001c0001t0023g0034 |
3 | HG02559.hp1 HG02615.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.846+1512_846+1513d others(4): Show |
AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993805 | |||||||
| chr10:4993952 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.846+1367T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4993952 | |||||||
| chr10:4994001 | A | G | 2 | a0001c0002t0031g0149 a0001c0002t0032g0150 |
2 | HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.846+1318T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994001 | |||||||
| chr10:4994016 | G | C | 23 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0029 others(20): Show |
85 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.846+1303C>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994016 | |||||||
| chr10:4994041 | A | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(68): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.846+1278T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994041 | |||||||
| chr10:4994137 | TATA | T | 1 | a0001c0001t0003g0021 | 3 | HG01106.hp1 HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.846+1179_846+1181d others(5): Show |
AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994137 | |||||||
| chr10:4994148 | T | C | 1 | a0003c0006t0001g0024 | 3 | HG01168.hp1 HG01169.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.846+1171A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994148 | |||||||
| chr10:4994152 | A | T | 2 | a0001c0005t0007g0042 a0001c0005t0027g0101 |
3 | HG02055.hp2 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.846+1167T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994152 | |||||||
| chr10:4994154 | G | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(102): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.846+1165C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994154 | |||||||
| chr10:4994177 | A | C | 6 | a0001c0002t0006g0151 a0001c0002t0006g0152 a0002c0004t0006g0006 others(3): Show |
18 | HG01109.hp2 HG01175.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.846+1142T>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994177 | |||||||
| chr10:4994249 | G | A | 22 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0029 others(19): Show |
84 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.846+1070C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994249 | |||||||
| chr10:4994269 | C | CAATT | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(149): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.846+1049_846+1050i others(6): Show |
AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994269 | |||||||
| chr10:4994363 | A | G | 34 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0029 others(31): Show |
112 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.846+956T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994363 | |||||||
| chr10:4994367 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(148): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.846+952G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994367 | |||||||
| chr10:4994421 | G | A | 1 | a0002c0004t0019g0033 | 2 | HG01109.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.846+898C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994421 | |||||||
| chr10:4994444 | C | G | 1 | a0001c0001t0001g0048 | 2 | NA18941.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.846+875G>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994444 | |||||||
| chr10:4994450 | G | A | 2 | a0001c0005t0010g0143 a0007c0014t0010g0144 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.846+869C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994450 | |||||||
| chr10:4994508 | T | C | 2 | a0001c0001t0003g0031 a0006c0016t0003g0079 |
3 | HG02818.hp2 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.846+811A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994508 | |||||||
| chr10:4994509 | G | A | 2 | a0001c0001t0003g0031 a0006c0016t0003g0079 |
3 | HG02818.hp2 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.846+810C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994509 | |||||||
| chr10:4994510 | T | G | 2 | a0001c0001t0003g0031 a0006c0016t0003g0079 |
3 | HG02818.hp2 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.846+809A>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994510 | |||||||
| chr10:4994573 | G | A | 1 | a0001c0001t0001g0050 | 2 | NA18939.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.846+746C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994573 | |||||||
| chr10:4994635 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(75): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.846+684T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994635 | |||||||
| chr10:4994792 | G | T | 2 | a0001c0002t0006g0151 a0001c0002t0006g0152 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.846+527C>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994792 | |||||||
| chr10:4994808 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.846+511A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994808 | |||||||
| chr10:4994812 | G | A | 15 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(12): Show |
35 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.846+507C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994812 | |||||||
| chr10:4994892 | C | CA | 39 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0029 others(36): Show |
122 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.846+426dupT | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994892 | |||||||
| chr10:4994923 | C | G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0108 others(7): Show |
34 | HG00621.hp1 HG01074.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.846+396G>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994923 | |||||||
| chr10:4994993 | C | T | 2 | a0001c0008t0008g0053 a0001c0008t0008g0054 |
2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.846+326G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4994993 | |||||||
| chr10:4995032 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.846+287A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4995032 | |||||||
| chr10:4995068 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(149): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.846+251A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4995068 | |||||||
| chr10:4995133 | A | T | 50 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0029 others(47): Show |
148 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.846+186T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4995133 | |||||||
| chr10:4995150 | C | T | 5 | a0001c0005t0010g0017 a0001c0005t0010g0018 a0001c0005t0010g0143 others(2): Show |
9 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.846+169G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4995150 | |||||||
| chr10:4995201 | A | G | 2 | a0001c0005t0010g0143 a0007c0014t0010g0144 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.846+118T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4995201 | |||||||
| chr10:4995242 | TC | T | 4 | a0001c0003t0009g0013 a0001c0003t0009g0038 a0001c0003t0009g0039 others(1): Show |
10 | HG00323.hp2 HG01123.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.846+76delG | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4995242 | |||||||
| chr10:4995275 | G | A | 2 | a0001c0005t0010g0143 a0007c0014t0010g0144 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.846+44C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 7/8 | chr10 | 4995275 | |||||||
| chr10:4995524 | C | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(68): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.681-40G>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 6/8 | chr10 | 4995524 | |||||||
| chr10:4995526 | A | G | 19 | a0001c0001t0003g0004 a0001c0001t0003g0020 a0001c0001t0003g0021 others(16): Show |
38 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.681-42T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 6/8 | chr10 | 4995526 | |||||||
| chr10:4995527 | T | TAC | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(68): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.681-44_681-43insGT | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 6/8 | chr10 | 4995527 | |||||||
| chr10:4995540 | G | A | 1 | a0001c0001t0022g0035 | 2 | HG01243.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.681-56C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 6/8 | chr10 | 4995540 | |||||||
| chr10:4995580 | C | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(61): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.681-96G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 6/8 | chr10 | 4995580 | |||||||
| chr10:4995721 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(52): Show |
152 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.680+35T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 6/8 | chr10 | 4995721 | |||||||
| chr10:4995722 | G | C | 4 | a0001c0003t0009g0013 a0001c0003t0009g0038 a0001c0003t0009g0039 others(1): Show |
10 | HG00323.hp2 HG01123.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.680+34C>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 6/8 | chr10 | 4995722 | |||||||
| chr10:4995913 | T | C | 23 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0029 others(20): Show |
85 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.571-48A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4995913 | |||||||
| chr10:4995919 | T | C | 1 | a0001c0001t0002g0064 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.571-54A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4995919 | |||||||
| chr10:4995957 | G | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(67): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.571-92C>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4995957 | |||||||
| chr10:4995987 | C | T | 1 | a0001c0003t0007g0037 | 2 | HG00140.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.571-122G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4995987 | |||||||
| chr10:4996104 | G | A | 2 | a0001c0001t0008g0045 a0001c0001t0008g0105 |
3 | HG02723.hp2 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.571-239C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996104 | |||||||
| chr10:4996115 | G | C | 9 | a0001c0001t0002g0008 a0001c0001t0008g0084 a0001c0001t0017g0065 others(6): Show |
20 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.571-250C>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996115 | |||||||
| chr10:4996228 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(89): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.571-363T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996228 | |||||||
| chr10:4996272 | A | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(54): Show |
155 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.571-407T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996272 | |||||||
| chr10:4996289 | A | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(52): Show |
152 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.571-424T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996289 | |||||||
| chr10:4996300 | C | CAT | 6 | a0001c0001t0008g0009 a0001c0001t0008g0045 a0001c0001t0008g0105 others(3): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.571-437_571-436dup others(2): Show |
AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996300 | |||||||
| chr10:4996323 | C | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(68): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.571-458G>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996323 | |||||||
| chr10:4996365 | T | C | 2 | a0001c0001t0002g0066 a0001c0001t0007g0088 |
2 | HG00597.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.571-500A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996365 | |||||||
| chr10:4996537 | A | T | 1 | a0001c0001t0002g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.571-672T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996537 | |||||||
| chr10:4996546 | T | TTATATA | 2 | a0001c0001t0001g0046 a0001c0001t0001g0104 |
3 | HG02080.hp2 NA18942.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.571-682_571-681ins others(6): Show |
AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996546 | |||||||
| chr10:4996547 | A | AAT | 15 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(12): Show |
35 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.571-684_571-683dup others(2): Show |
AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996547 | |||||||
| chr10:4996547 | A | AATATAT | 53 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(50): Show |
150 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.571-688_571-683dup others(6): Show |
AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996547 | |||||||
| chr10:4996547 | A | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0104 |
3 | HG02080.hp2 NA18942.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.571-682T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996547 | |||||||
| chr10:4996637 | C | T | 17 | a0001c0001t0002g0066 a0001c0001t0004g0100 a0001c0002t0005g0005 others(14): Show |
37 | HG00140.hp2 HG00597.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.571-772G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996637 | |||||||
| chr10:4996639 | A | G | 4 | a0001c0003t0009g0013 a0001c0003t0009g0038 a0001c0003t0009g0039 others(1): Show |
10 | HG00323.hp2 HG01123.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.571-774T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996639 | |||||||
| chr10:4996688 | G | T | 1 | a0001c0001t0042g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.571-823C>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996688 | |||||||
| chr10:4996742 | T | C | 2 | a0001c0001t0002g0066 a0001c0001t0004g0100 |
2 | HG00597.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.571-877A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996742 | |||||||
| chr10:4996751 | T | C | 2 | a0001c0001t0002g0066 a0001c0001t0004g0100 |
2 | HG00597.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.571-886A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996751 | |||||||
| chr10:4996798 | T | C | 5 | a0001c0001t0002g0066 a0001c0001t0004g0100 a0001c0001t0023g0034 others(2): Show |
6 | HG00597.hp2 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-933A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996798 | |||||||
| chr10:4996928 | T | C | 3 | a0001c0005t0010g0017 a0001c0005t0010g0018 a0001c0005t0025g0056 |
7 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.571-1063A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996928 | |||||||
| chr10:4996973 | G | T | 1 | a0001c0001t0001g0118 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.571-1108C>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996973 | |||||||
| chr10:4996976 | A | C | 7 | a0001c0003t0007g0011 a0001c0003t0007g0037 a0001c0003t0007g0090 others(4): Show |
19 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.571-1111T>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4996976 | |||||||
| chr10:4997003 | C | A | 1 | a0001c0001t0002g0060 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.571-1138G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997003 | |||||||
| chr10:4997046 | T | G | 1 | a0001c0001t0002g0067 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.571-1181A>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997046 | |||||||
| chr10:4997071 | T | TAGCTTAA others(412): Show |
1 | a0001c0001t0002g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.571-1207_571-1206i others(421): Show |
AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997071 | |||||||
| chr10:4997073 | G | A | 1 | a0001c0001t0007g0088 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.571-1208C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997073 | |||||||
| chr10:4997103 | C | A | 1 | a0001c0001t0002g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.571-1238G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997103 | |||||||
| chr10:4997132 | A | C | 1 | a0001c0001t0001g0117 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.571-1267T>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997132 | |||||||
| chr10:4997142 | C | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(116): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.571-1277G>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997142 | |||||||
| chr10:4997174 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.571-1309G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997174 | |||||||
| chr10:4997187 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.571-1322G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997187 | |||||||
| chr10:4997192 | T | G | 1 | a0001c0001t0002g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.571-1327A>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997192 | |||||||
| chr10:4997199 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.571-1334G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997199 | |||||||
| chr10:4997213 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.571-1348A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997213 | |||||||
| chr10:4997218 | A | T | 1 | a0001c0001t0002g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.571-1353T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997218 | |||||||
| chr10:4997229 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.571-1364A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997229 | |||||||
| chr10:4997240 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.571-1375C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997240 | |||||||
| chr10:4997324 | C | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(54): Show |
155 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.570+1301G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997324 | |||||||
| chr10:4997350 | T | G | 1 | a0001c0001t0002g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.570+1275A>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997350 | |||||||
| chr10:4997359 | A | C | 1 | a0001c0001t0002g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.570+1266T>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997359 | |||||||
| chr10:4997370 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.570+1255G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997370 | |||||||
| chr10:4997372 | G | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(54): Show |
155 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.570+1253C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997372 | |||||||
| chr10:4997387 | A | G | 2 | a0001c0001t0002g0066 a0002c0004t0006g0006 |
12 | HG00597.hp2 HG01243.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.570+1238T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997387 | |||||||
| chr10:4997399 | A | G | 1 | a0001c0001t0002g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.570+1226T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997399 | |||||||
| chr10:4997408 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.570+1217G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997408 | |||||||
| chr10:4997514 | A | G | 7 | a0001c0003t0007g0011 a0001c0003t0007g0037 a0001c0003t0007g0090 others(4): Show |
19 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.570+1111T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997514 | |||||||
| chr10:4997572 | G | A | 3 | a0001c0001t0002g0008 a0001c0001t0008g0084 a0001c0001t0017g0065 |
9 | NA18944.hp2 NA18968.hp1 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.570+1053C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997572 | |||||||
| chr10:4997599 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.570+1026G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997599 | |||||||
| chr10:4997723 | A | G | 1 | a0003c0006t0001g0024 | 3 | HG01168.hp1 HG01169.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.570+902T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997723 | |||||||
| chr10:4997728 | C | T | 1 | a0001c0001t0002g0059 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.570+897G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997728 | |||||||
| chr10:4997775 | T | C | 1 | a0001c0002t0006g0152 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.570+850A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997775 | |||||||
| chr10:4997811 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(71): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.570+814C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997811 | |||||||
| chr10:4997843 | A | G | 2 | a0001c0001t0022g0035 a0001c0001t0023g0034 |
4 | HG01243.hp1 HG02615.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+782T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997843 | |||||||
| chr10:4997905 | A | G | 4 | a0002c0004t0006g0006 a0002c0004t0006g0032 a0002c0004t0019g0033 others(1): Show |
16 | HG01109.hp2 HG01175.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.570+720T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997905 | |||||||
| chr10:4997955 | C | T | 5 | a0001c0005t0010g0017 a0001c0005t0010g0018 a0001c0005t0010g0143 others(2): Show |
9 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.570+670G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997955 | |||||||
| chr10:4997969 | C | T | 2 | a0001c0002t0005g0052 a0001c0015t0005g0155 |
3 | HG02132.hp2 NA18971.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.570+656G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997969 | |||||||
| chr10:4997980 | G | T | 1 | a0004c0011t0007g0148 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.570+645C>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4997980 | |||||||
| chr10:4998010 | C | G | 2 | a0001c0001t0003g0072 a0001c0001t0044g0071 |
2 | HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.570+615G>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4998010 | |||||||
| chr10:4998021 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(71): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.570+604A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4998021 | |||||||
| chr10:4998159 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(102): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.570+466A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4998159 | |||||||
| chr10:4998161 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(102): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.570+464A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4998161 | |||||||
| chr10:4998162 | C | A | 2 | a0001c0005t0010g0143 a0007c0014t0010g0144 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.570+463G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4998162 | |||||||
| chr10:4998168 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(102): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.570+457T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4998168 | |||||||
| chr10:4998249 | C | T | 4 | a0002c0004t0006g0006 a0002c0004t0006g0032 a0002c0004t0019g0033 others(1): Show |
16 | HG01109.hp2 HG01175.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.570+376G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4998249 | |||||||
| chr10:4998260 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(70): Show |
191 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.570+365A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4998260 | |||||||
| chr10:4998326 | G | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(147): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.570+299C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4998326 | |||||||
| chr10:4998445 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(70): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.570+180G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4998445 | |||||||
| chr10:4998480 | A | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(71): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.570+145T>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4998480 | |||||||
| chr10:4998545 | A | T | 4 | a0002c0004t0006g0006 a0002c0004t0006g0032 a0002c0004t0019g0033 others(1): Show |
16 | HG01109.hp2 HG01175.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.570+80T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 5/8 | chr10 | 4998545 | |||||||
| chr10:4998817 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.448-70G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 4/8 | chr10 | 4998817 | |||||||
| chr10:4998841 | C | T | 4 | a0002c0004t0006g0006 a0002c0004t0006g0032 a0002c0004t0019g0033 others(1): Show |
16 | HG01109.hp2 HG01175.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.448-94G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 4/8 | chr10 | 4998841 | |||||||
| chr10:4998847 | A | C | 1 | a0001c0001t0049g0058 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.448-100T>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 4/8 | chr10 | 4998847 | |||||||
| chr10:4998949 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0113 |
2 | HG00408.hp1 HG00438.hp1 |
intron_variant | MODIFIER | c.448-202T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 4/8 | chr10 | 4998949 | |||||||
| chr10:4998955 | G | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0113 |
2 | HG00408.hp1 HG00438.hp1 |
intron_variant | MODIFIER | c.448-208C>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 4/8 | chr10 | 4998955 | |||||||
| chr10:4998967 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0113 |
2 | HG00408.hp1 HG00438.hp1 |
intron_variant | MODIFIER | c.448-220T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 4/8 | chr10 | 4998967 | |||||||
| chr10:4998970 | T | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0113 |
2 | HG00408.hp1 HG00438.hp1 |
intron_variant | MODIFIER | c.448-223A>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 4/8 | chr10 | 4998970 | |||||||
| chr10:4998972 | C | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0113 |
2 | HG00408.hp1 HG00438.hp1 |
intron_variant | MODIFIER | c.448-225G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 4/8 | chr10 | 4998972 | |||||||
| chr10:4998984 | G | T | 2 | a0001c0001t0001g0102 a0001c0001t0001g0113 |
2 | HG00408.hp1 HG00438.hp1 |
intron_variant | MODIFIER | c.447+216C>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 4/8 | chr10 | 4998984 | |||||||
| chr10:4999104 | C | A | 13 | a0001c0001t0004g0007 a0001c0001t0004g0012 a0001c0001t0004g0086 others(10): Show |
30 | HG00280.hp1 HG00323.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.447+96G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 4/8 | chr10 | 4999104 | |||||||
| chr10:4999122 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.447+78A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 4/8 | chr10 | 4999122 | |||||||
| chr10:4999183 | C | T | 13 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(10): Show |
33 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.447+17G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 4/8 | chr10 | 4999183 | |||||||
| chr10:4999385 | C | T | 5 | a0001c0005t0010g0017 a0001c0005t0010g0018 a0001c0005t0010g0143 others(2): Show |
9 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.370-108G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 4999385 | |||||||
| chr10:4999402 | G | A | 17 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(14): Show |
37 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.370-125C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 4999402 | |||||||
| chr10:4999411 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.370-134T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 4999411 | |||||||
| chr10:4999466 | A | G | 3 | a0001c0003t0007g0011 a0001c0003t0007g0037 a0001c0003t0007g0090 |
9 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.370-189T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 4999466 | |||||||
| chr10:4999486 | G | T | 1 | a0001c0001t0001g0111 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.370-209C>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 4999486 | |||||||
| chr10:4999488 | A | G | 4 | a0002c0004t0006g0006 a0002c0004t0006g0032 a0002c0004t0019g0033 others(1): Show |
16 | HG01109.hp2 HG01175.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.370-211T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 4999488 | |||||||
| chr10:4999663 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.370-386T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 4999663 | |||||||
| chr10:4999688 | T | G | 2 | a0001c0001t0008g0009 a0001c0001t0047g0106 |
8 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.370-411A>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 4999688 | |||||||
| chr10:4999724 | C | T | 32 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0029 others(29): Show |
102 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.370-447G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 4999724 | |||||||
| chr10:4999731 | C | A | 28 | a0001c0001t0001g0025 a0001c0001t0002g0002 a0001c0001t0002g0008 others(25): Show |
93 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.370-454G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 4999731 | |||||||
| chr10:4999736 | T | C | 1 | a0001c0002t0005g0158 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.370-459A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 4999736 | |||||||
| chr10:4999840 | T | C | 2 | a0001c0001t0002g0029 a0001c0001t0046g0057 |
3 | HG02040.hp1 NA18989.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.370-563A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 4999840 | |||||||
| chr10:4999899 | GT | G | 2 | a0001c0001t0002g0030 a0001c0001t0002g0067 |
3 | HG00544.hp1 HG00544.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.370-623delA | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 4999899 | |||||||
| chr10:4999900 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.370-623A>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 4999900 | |||||||
| chr10:5000083 | C | T | 1 | a0001c0001t0007g0088 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.369+467G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 5000083 | |||||||
| chr10:5000102 | T | C | 14 | a0001c0001t0004g0007 a0001c0001t0004g0012 a0001c0001t0004g0041 others(11): Show |
32 | HG00280.hp1 HG00323.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.369+448A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 5000102 | |||||||
| chr10:5000106 | A | G | 3 | a0001c0005t0010g0017 a0001c0005t0010g0018 a0001c0005t0025g0056 |
7 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.369+444T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 5000106 | |||||||
| chr10:5000124 | A | T | 17 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(14): Show |
37 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.369+426T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 5000124 | |||||||
| chr10:5000128 | A | G | 3 | a0001c0003t0007g0011 a0001c0003t0007g0037 a0001c0003t0007g0090 |
9 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.369+422T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 5000128 | |||||||
| chr10:5000264 | A | C | 1 | a0001c0001t0033g0109 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.369+286T>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 5000264 | |||||||
| chr10:5000401 | A | G | 1 | a0004c0010t0003g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.369+149T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 5000401 | |||||||
| chr10:5000472 | C | T | 22 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0029 others(19): Show |
84 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.369+78G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 5000472 | |||||||
| chr10:5000490 | G | A | 1 | a0001c0001t0013g0068 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.369+60C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 3/8 | chr10 | 5000490 | |||||||
| chr10:5000685 | C | G | 4 | a0001c0002t0006g0151 a0001c0002t0006g0152 a0001c0002t0031g0149 others(1): Show |
4 | HG03041.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-19G>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 2/8 | chr10 | 5000685 | |||||||
| chr10:5000928 | C | T | 3 | a0001c0003t0007g0011 a0001c0003t0007g0037 a0001c0003t0007g0090 |
9 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-262G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 2/8 | chr10 | 5000928 | |||||||
| chr10:5001039 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.253-373T>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 2/8 | chr10 | 5001039 | |||||||
| chr10:5001102 | A | G | 2 | a0001c0005t0007g0042 a0001c0005t0027g0101 |
3 | HG02055.hp2 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.252+412T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 2/8 | chr10 | 5001102 | |||||||
| chr10:5001136 | C | T | 24 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(21): Show |
56 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.252+378G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 2/8 | chr10 | 5001136 | |||||||
| chr10:5001178 | G | A | 4 | a0002c0004t0006g0006 a0002c0004t0006g0032 a0002c0004t0019g0033 others(1): Show |
16 | HG01109.hp2 HG01175.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.252+336C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 2/8 | chr10 | 5001178 | |||||||
| chr10:5001196 | G | C | 17 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(14): Show |
37 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.252+318C>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 2/8 | chr10 | 5001196 | |||||||
| chr10:5001199 | A | C | 1 | a0001c0001t0003g0020 | 3 | HG00639.hp2 HG01361.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.252+315T>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 2/8 | chr10 | 5001199 | |||||||
| chr10:5001219 | A | G | 1 | a0001c0001t0045g0089 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.252+295T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 2/8 | chr10 | 5001219 | |||||||
| chr10:5001232 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.252+282T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 2/8 | chr10 | 5001232 | |||||||
| chr10:5001291 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.252+223C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 2/8 | chr10 | 5001291 | |||||||
| chr10:5001294 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.252+220C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 2/8 | chr10 | 5001294 | |||||||
| chr10:5001312 | G | A | 9 | a0001c0001t0004g0007 a0001c0001t0004g0012 a0001c0001t0004g0041 others(6): Show |
25 | HG00280.hp1 HG00323.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.252+202C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 2/8 | chr10 | 5001312 | |||||||
| chr10:5001682 | C | G | 1 | a0001c0003t0007g0090 | 1 | HG02602.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.85-1G>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5001682 | |||||||
| chr10:5001796 | T | C | 1 | a0001c0001t0002g0069 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.85-115A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5001796 | |||||||
| chr10:5001812 | C | T | 1 | a0001c0001t0045g0089 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.85-131G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5001812 | |||||||
| chr10:5001841 | T | G | 17 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(14): Show |
37 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.85-160A>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5001841 | |||||||
| chr10:5001904 | A | G | 15 | a0001c0001t0003g0004 a0001c0001t0003g0020 a0001c0001t0003g0021 others(12): Show |
33 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.85-223T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5001904 | |||||||
| chr10:5001996 | A | G | 2 | a0001c0005t0007g0042 a0001c0005t0027g0101 |
3 | HG02055.hp2 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.85-315T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5001996 | |||||||
| chr10:5002045 | G | A | 1 | a0001c0008t0008g0054 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.85-364C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5002045 | |||||||
| chr10:5002099 | A | G | 22 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0029 others(19): Show |
84 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.85-418T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5002099 | |||||||
| chr10:5002154 | G | A | 1 | a0001c0001t0042g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.85-473C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5002154 | |||||||
| chr10:5002280 | C | T | 22 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0029 others(19): Show |
84 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.85-599G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5002280 | |||||||
| chr10:5002322 | T | C | 1 | a0001c0001t0001g0044 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.85-641A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5002322 | |||||||
| chr10:5002464 | A | G | 1 | a0001c0001t0007g0088 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.85-783T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5002464 | |||||||
| chr10:5002470 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.85-789C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5002470 | |||||||
| chr10:5002566 | AT | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(54): Show |
155 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.85-886delA | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5002566 | |||||||
| chr10:5002983 | A | G | 2 | a0001c0001t0022g0035 a0001c0001t0023g0034 |
4 | HG01243.hp1 HG02615.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+769T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5002983 | |||||||
| chr10:5002998 | A | T | 1 | a0001c0001t0046g0057 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.84+754T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5002998 | |||||||
| chr10:5003063 | A | G | 2 | a0004c0010t0003g0147 a0004c0011t0007g0148 |
2 | HG01255.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.84+689T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003063 | |||||||
| chr10:5003157 | C | A | 2 | a0001c0005t0010g0143 a0007c0014t0010g0144 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.84+595G>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003157 | |||||||
| chr10:5003183 | A | G | 3 | a0001c0005t0010g0017 a0001c0005t0010g0018 a0001c0005t0025g0056 |
7 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.84+569T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003183 | |||||||
| chr10:5003187 | T | G | 1 | a0001c0001t0002g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.84+565A>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003187 | |||||||
| chr10:5003189 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.84+563G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003189 | |||||||
| chr10:5003195 | T | G | 2 | a0001c0001t0022g0035 a0001c0001t0023g0034 |
4 | HG01243.hp1 HG02615.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+557A>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003195 | |||||||
| chr10:5003196 | T | A | 19 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(16): Show |
39 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.84+556A>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003196 | |||||||
| chr10:5003204 | G | GT | 4 | a0001c0001t0008g0105 a0001c0001t0020g0036 a0001c0005t0010g0017 others(1): Show |
7 | HG02145.hp2 HG02280.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.84+547dupA | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003204 | |||||||
| chr10:5003204 | GT | G | 5 | a0001c0001t0002g0055 a0001c0001t0002g0083 a0001c0001t0007g0043 others(2): Show |
7 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.84+547delA | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003204 | |||||||
| chr10:5003204 | GTTTT | G | 19 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(16): Show |
39 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.84+544_84+547delAA others(2): Show |
AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003204 | |||||||
| chr10:5003207 | T | A | 1 | a0001c0001t0002g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.84+545A>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003207 | |||||||
| chr10:5003210 | T | A | 19 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(16): Show |
39 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.84+542A>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003210 | |||||||
| chr10:5003241 | T | C | 20 | a0001c0001t0001g0104 a0001c0002t0005g0005 a0001c0002t0005g0051 others(17): Show |
40 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.84+511A>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003241 | |||||||
| chr10:5003242 | A | G | 20 | a0001c0001t0001g0104 a0001c0002t0005g0005 a0001c0002t0005g0051 others(17): Show |
40 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.84+510T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003242 | |||||||
| chr10:5003280 | G | A | 20 | a0001c0001t0001g0145 a0001c0002t0005g0005 a0001c0002t0005g0051 others(17): Show |
40 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.84+472C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003280 | |||||||
| chr10:5003303 | TAGTATTA others(1): Show |
T | 2 | a0001c0001t0022g0035 a0001c0001t0023g0034 |
4 | HG01243.hp1 HG02615.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+441_84+448delGT others(6): Show |
AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003303 | |||||||
| chr10:5003327 | G | T | 1 | a0001c0001t0042g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.84+425C>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003327 | |||||||
| chr10:5003330 | G | A | 18 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(15): Show |
38 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.84+422C>T | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003330 | |||||||
| chr10:5003357 | A | G | 19 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(16): Show |
39 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.84+395T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003357 | |||||||
| chr10:5003369 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0103 |
3 | HG03710.hp2 HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.84+383G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003369 | |||||||
| chr10:5003458 | A | C | 1 | a0001c0001t0002g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.84+294T>G | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003458 | |||||||
| chr10:5003508 | A | G | 19 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(16): Show |
39 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.84+244T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003508 | |||||||
| chr10:5003511 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.84+241G>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003511 | |||||||
| chr10:5003531 | T | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(60): Show |
167 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.84+221A>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003531 | |||||||
| chr10:5003557 | A | G | 1 | a0001c0001t0004g0086 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.84+195T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003557 | |||||||
| chr10:5003559 | A | T | 1 | a0001c0001t0002g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.84+193T>A | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003559 | |||||||
| chr10:5003640 | C | G | 1 | a0001c0001t0001g0085 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.84+112G>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003640 | |||||||
| chr10:5003642 | T | G | 19 | a0001c0002t0005g0005 a0001c0002t0005g0051 a0001c0002t0005g0052 others(16): Show |
39 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.84+110A>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003642 | |||||||
| chr10:5003670 | A | G | 45 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0002g0002 others(42): Show |
141 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.84+82T>C | AKR1C2 | ENSG00000151632.18 | transcript | ENST00000380753.9 | protein_coding | 1/8 | chr10 | 5003670 |