Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79758 |
| ensemblid | ENSG00000102796.12 |
| hgncid | 25832 |
| symbol | DHRS12 |
| name | dehydrogenase/reductase 12 |
| refseq_nuc | NM_001377533.1 |
| refseq_prot | NP_001364462.1 |
| ensembl_nuc | ENST00000444610.8 |
| ensembl_prot | ENSP00000411565.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 51767993 |
| end | 51804163 |
| strand | - |
| ver | v1.2 |
| region | chr13:51767993-51804163 |
| region5000 | chr13:51762993-51809163 |
| regionname0 | DHRS12_chr13_51767993_51804163 |
| regionname5000 | DHRS12_chr13_51762993_51809163 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 268 | 329 | 68 | 40 | 173 | 14 | 33 | 137 | DHRS12_chr13_51762993_51809163 | DHRS12 | MNLHV others(263): Show |
chr13 | 51762993 | 51809163 |
| a0002 | 0/0 | 268 | 51 | 24 | 23 | 0 | 0 | 4 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | MNLHV others(263): Show |
chr13 | 51762993 | 51809163 |
| a0003 | 0/1 | 268 | 35 | 1 | 15 | 9 | 2 | 7 | 6 | DHRS12_chr13_51762993_51809163 | DHRS12 | MNLHV others(263): Show |
chr13 | 51762993 | 51809163 |
| a0004 | 0/0 | 268 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | MNLHV others(263): Show |
chr13 | 51762993 | 51809163 |
| a0005 | 0/0 | 268 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | MNLQV others(263): Show |
chr13 | 51762993 | 51809163 |
| a0006 | 0/0 | 268 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | MNLHV others(263): Show |
chr13 | 51762993 | 51809163 |
| a0007 | 0/0 | 268 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | MNLHV others(263): Show |
chr13 | 51762993 | 51809163 |
| a0008 | 0/0 | 268 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | MNLHV others(263): Show |
chr13 | 51762993 | 51809163 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 804 | 326 | 67 | 40 | 173 | 14 | 31 | DHRS12_chr13_51762993_51809163 | DHRS12 | ATGAA others(799): Show |
chr13 | 51762993 | 51809163 | ||
| a0001c0004 | 0/0 | 804 | 3 | 1 | 0 | 0 | 0 | 2 | DHRS12_chr13_51762993_51809163 | DHRS12 | ATGAA others(799): Show |
chr13 | 51762993 | 51809163 | ||
| a0002c0002 | 0/0 | 804 | 50 | 24 | 22 | 0 | 0 | 4 | DHRS12_chr13_51762993_51809163 | DHRS12 | ATGAA others(799): Show |
chr13 | 51762993 | 51809163 | ||
| a0002c0010 | 0/0 | 804 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | ATGAA others(799): Show |
chr13 | 51762993 | 51809163 | ||
| a0003c0003 | 0/1 | 804 | 35 | 1 | 15 | 9 | 2 | 7 | DHRS12_chr13_51762993_51809163 | DHRS12 | ATGAA others(799): Show |
chr13 | 51762993 | 51809163 | ||
| a0004c0008 | 0/0 | 804 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | ATGAA others(799): Show |
chr13 | 51762993 | 51809163 | ||
| a0005c0005 | 0/0 | 804 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | ATGAA others(799): Show |
chr13 | 51762993 | 51809163 | ||
| a0006c0007 | 0/0 | 804 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | ATGAA others(799): Show |
chr13 | 51762993 | 51809163 | ||
| a0007c0006 | 0/0 | 804 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | ATGAA others(799): Show |
chr13 | 51762993 | 51809163 | ||
| a0008c0009 | 0/0 | 804 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | ATGAA others(799): Show |
chr13 | 51762993 | 51809163 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1119 | 244 | 55 | 31 | 126 | 9 | 22 | DHRS12_chr13_51762993_51809163 | DHRS12 | AGGGC others(1114): Show |
chr13 | 51762993 | 51809163 |
| a0001c0001t0002 | 0/0 | 1119 | 60 | 1 | 8 | 37 | 5 | 9 | DHRS12_chr13_51762993_51809163 | DHRS12 | AGGGC others(1114): Show |
chr13 | 51762993 | 51809163 |
| a0001c0001t0003 | 0/0 | 1116 | 12 | 1 | 1 | 10 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | AGGGC others(1111): Show |
chr13 | 51762993 | 51809163 |
| a0001c0001t0004 | 0/0 | 1118 | 8 | 8 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | AGGGC others(1113): Show |
chr13 | 51762993 | 51809163 |
| a0001c0001t0007 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | AGGGC others(1114): Show |
chr13 | 51762993 | 51809163 |
| a0001c0001t0008 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | AGGGC others(1114): Show |
chr13 | 51762993 | 51809163 |
| a0001c0004t0001 | 0/0 | 1119 | 3 | 1 | 0 | 0 | 0 | 2 | DHRS12_chr13_51762993_51809163 | DHRS12 | AGGGC others(1114): Show |
chr13 | 51762993 | 51809163 |
| a0002c0002t0001 | 0/0 | 1119 | 2 | 1 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | AGGGC others(1114): Show |
chr13 | 51762993 | 51809163 |
| a0002c0002t0003 | 0/0 | 1116 | 47 | 22 | 22 | 0 | 0 | 3 | DHRS12_chr13_51762993_51809163 | DHRS12 | AGGGC others(1111): Show |
chr13 | 51762993 | 51809163 |
| a0002c0002t0006 | 0/0 | 1115 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | AGGGC others(1110): Show |
chr13 | 51762993 | 51809163 |
| a0002c0010t0003 | 0/0 | 1116 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | AGGGC others(1111): Show |
chr13 | 51762993 | 51809163 |
| a0003c0003t0001 | 0/1 | 1119 | 30 | 1 | 15 | 6 | 2 | 5 | DHRS12_chr13_51762993_51809163 | DHRS12 | AGGGC others(1114): Show |
chr13 | 51762993 | 51809163 |
| a0003c0003t0002 | 0/0 | 1119 | 2 | 0 | 0 | 0 | 0 | 2 | DHRS12_chr13_51762993_51809163 | DHRS12 | AGGGC others(1114): Show |
chr13 | 51762993 | 51809163 |
| a0003c0003t0005 | 0/0 | 1116 | 3 | 0 | 0 | 3 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | AGGGC others(1111): Show |
chr13 | 51762993 | 51809163 |
| a0004c0008t0002 | 0/0 | 1119 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | AGGGC others(1114): Show |
chr13 | 51762993 | 51809163 |
| a0005c0005t0001 | 0/0 | 1119 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | AGGGC others(1114): Show |
chr13 | 51762993 | 51809163 |
| a0006c0007t0001 | 0/0 | 1119 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | AGGGC others(1114): Show |
chr13 | 51762993 | 51809163 |
| a0007c0006t0004 | 0/0 | 1118 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | AGGGC others(1113): Show |
chr13 | 51762993 | 51809163 |
| a0008c0009t0002 | 0/0 | 1119 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | AGGGC others(1114): Show |
chr13 | 51762993 | 51809163 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0008 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0057 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0053 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0056 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0061 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0003g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0004g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0004g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0001t0008g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0004t0001g0047 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0001c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0003g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0002t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0002c0010t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0238 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0003c0003t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0004c0008t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0005c0005t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0006c0007t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0007c0006t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| a0008c0009t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | GBR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | GBR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | FIN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0273 | EUR | FIN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00323 | hp2 | a0003 | c0003 | t0001 | g0236 | EUR | FIN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | CHS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | CHS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | CHS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00558 | hp2 | a0003 | c0003 | t0001 | g0203 | EAS | CHS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00597 | hp1 | a0003 | c0003 | t0001 | g0145 | EAS | CHS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | CHS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00639 | hp2 | a0003 | c0003 | t0001 | g0016 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0259 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00738 | hp1 | a0003 | c0003 | t0001 | g0032 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0265 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0318 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01070 | hp2 | a0003 | c0003 | t0001 | g0204 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01081 | hp1 | a0003 | c0003 | t0001 | g0220 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01081 | hp2 | a0002 | c0002 | t0003 | g0050 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01106 | hp1 | a0002 | c0002 | t0003 | g0320 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01106 | hp2 | a0002 | c0002 | t0003 | g0249 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01109 | hp1 | a0002 | c0002 | t0003 | g0050 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01109 | hp2 | a0002 | c0010 | t0003 | g0253 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01168 | hp1 | a0003 | c0003 | t0001 | g0032 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01243 | hp1 | a0002 | c0002 | t0003 | g0042 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01255 | hp1 | a0002 | c0002 | t0003 | g0049 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01255 | hp2 | a0002 | c0002 | t0003 | g0158 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01256 | hp1 | a0003 | c0003 | t0001 | g0045 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01256 | hp2 | a0003 | c0003 | t0001 | g0041 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0319 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01258 | hp2 | a0003 | c0003 | t0001 | g0045 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01261 | hp2 | a0002 | c0002 | t0003 | g0255 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0171 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01361 | hp2 | a0002 | c0002 | t0003 | g0232 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01433 | hp1 | a0003 | c0003 | t0001 | g0041 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01496 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | IBS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0250 | EUR | IBS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0287 | EUR | IBS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | IBS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0156 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01891 | hp1 | a0002 | c0002 | t0003 | g0073 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01934 | hp1 | a0002 | c0002 | t0003 | g0251 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01934 | hp2 | a0003 | c0003 | t0001 | g0237 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01943 | hp1 | a0002 | c0002 | t0003 | g0231 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01952 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01975 | hp1 | a0002 | c0002 | t0003 | g0159 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01975 | hp2 | a0003 | c0003 | t0001 | g0223 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01978 | hp1 | a0003 | c0003 | t0001 | g0016 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01978 | hp2 | a0002 | c0002 | t0003 | g0246 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01981 | hp1 | a0004 | c0008 | t0002 | g0270 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01981 | hp2 | a0005 | c0005 | t0001 | g0200 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01993 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02004 | hp1 | a0002 | c0002 | t0003 | g0044 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02004 | hp2 | a0002 | c0002 | t0003 | g0080 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02015 | hp1 | a0006 | c0007 | t0001 | g0090 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02027 | hp2 | a0003 | c0003 | t0001 | g0205 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02055 | hp1 | a0002 | c0002 | t0003 | g0017 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02055 | hp2 | a0003 | c0003 | t0001 | g0239 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02145 | hp2 | a0002 | c0002 | t0003 | g0244 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02148 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02148 | hp2 | a0002 | c0002 | t0003 | g0049 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CDX | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CDX | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02258 | hp1 | a0002 | c0002 | t0003 | g0192 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02273 | hp1 | a0003 | c0003 | t0001 | g0222 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02273 | hp2 | a0002 | c0002 | t0003 | g0252 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02293 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02293 | hp2 | a0003 | c0003 | t0001 | g0016 | AMR | PEL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02572 | hp1 | a0002 | c0002 | t0003 | g0154 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02572 | hp2 | a0002 | c0002 | t0006 | g0063 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02615 | hp1 | a0002 | c0002 | t0003 | g0207 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02630 | hp2 | a0002 | c0002 | t0003 | g0189 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0314 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02698 | hp1 | a0002 | c0002 | t0003 | g0044 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02698 | hp2 | a0003 | c0003 | t0002 | g0248 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02723 | hp2 | a0002 | c0002 | t0003 | g0175 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02735 | hp1 | a0003 | c0003 | t0001 | g0221 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0193 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02896 | hp1 | a0002 | c0002 | t0003 | g0209 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02922 | hp1 | a0002 | c0002 | t0003 | g0190 | AFR | ESN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02976 | hp2 | a0002 | c0002 | t0003 | g0176 | AFR | ESN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0328 | AFR | MSL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03130 | hp1 | a0002 | c0002 | t0003 | g0157 | AFR | ESN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | ESN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03195 | hp1 | a0002 | c0002 | t0003 | g0074 | AFR | ESN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0064 | AFR | ESN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03209 | hp2 | a0007 | c0006 | t0004 | g0062 | AFR | MSL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03453 | hp1 | a0002 | c0002 | t0003 | g0017 | AFR | MSL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03453 | hp2 | a0002 | c0002 | t0003 | g0174 | AFR | MSL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03486 | hp1 | a0002 | c0002 | t0003 | g0042 | AFR | MSL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03492 | hp1 | a0003 | c0003 | t0001 | g0046 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03516 | hp2 | a0002 | c0002 | t0003 | g0217 | AFR | ESN | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0065 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03579 | hp1 | a0002 | c0002 | t0003 | g0218 | AFR | MSL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0066 | AFR | MSL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0283 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03669 | hp1 | a0003 | c0003 | t0001 | g0327 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03688 | hp1 | a0003 | c0003 | t0002 | g0201 | SAS | STU | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03688 | hp2 | a0002 | c0002 | t0003 | g0324 | SAS | STU | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0261 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03710 | hp2 | a0003 | c0003 | t0001 | g0046 | SAS | PJL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03831 | hp1 | a0001 | c0004 | t0001 | g0047 | SAS | BEB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0300 | SAS | BEB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03834 | hp2 | a0001 | c0004 | t0001 | g0208 | SAS | BEB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG04184 | hp2 | a0002 | c0002 | t0003 | g0141 | SAS | BEB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | STU | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0303 | SAS | STU | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | STU | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG04228 | hp1 | a0003 | c0003 | t0001 | g0202 | SAS | STU | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | STU | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | YRI | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18906 | hp2 | a0002 | c0002 | t0003 | g0072 | AFR | YRI | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18952 | hp1 | a0008 | c0009 | t0002 | g0311 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18979 | hp2 | a0003 | c0003 | t0005 | g0243 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18980 | hp1 | a0003 | c0003 | t0001 | g0170 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18982 | hp2 | a0003 | c0003 | t0001 | g0240 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18984 | hp2 | a0003 | c0003 | t0001 | g0316 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18993 | hp1 | a0003 | c0003 | t0005 | g0241 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19084 | hp2 | a0003 | c0003 | t0005 | g0242 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | YRI | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA20129 | hp1 | a0002 | c0002 | t0003 | g0228 | AFR | ASW | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0308 | AFR | ASW | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0230 | EUR | TSI | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA20805 | hp1 | a0003 | c0003 | t0001 | g0235 | EUR | TSI | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0211 | EUR | TSI | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | GIH | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | GIH | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02486 | hp1 | a0001 | c0004 | t0001 | g0047 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02486 | hp2 | a0002 | c0002 | t0003 | g0247 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02559 | hp1 | a0002 | c0002 | t0003 | g0017 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0191 | AFR | USA | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | USA | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0001 | g0238 | REF | REF | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0227 | REF | REF | DHRS12_chr13_51762993_51809163 | DHRS12 | chr13 | 51762993 | 51809163 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51769174 | T | C | 1 | a0004 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.679A>G | p.Ser227Gly | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 8/9 | 797/1119 | 679/807 | 227/268 | chr13 | 51769174 | |||
| chr13:51769248 | C | T | 1 | a0006 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.605G>A | p.Arg202His | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 8/9 | 723/1119 | 605/807 | 202/268 | chr13 | 51769248 | |||
| chr13:51769255 | C | T | 1 | a0002 | 51 | HG01081.hp2 HG01106.hp1 HG01106.hp2 others(48): Show |
missense_variant | MODERATE | c.598G>A | p.Gly200Arg | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 8/9 | 716/1119 | 598/807 | 200/268 | chr13 | 51769255 | |||
| chr13:51769265 | G | C | 1 | a0008 | 1 | NA18952.hp1 | missense_variant | MODERATE | c.588C>G | p.His196Gln | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 8/9 | 706/1119 | 588/807 | 196/268 | chr13 | 51769265 | |||
| chr13:51790076 | C | T | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.236G>A | p.Cys79Tyr | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/9 | 354/1119 | 236/807 | 79/268 | chr13 | 51790076 | |||
| chr13:51791218 | G | T | 2 | a0003 a0005 |
36 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(33): Show |
missense_variant | MODERATE | c.166C>A | p.Gln56Lys | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 3/9 | 284/1119 | 166/807 | 56/268 | chr13 | 51791218 | |||
| chr13:51799648 | A | C | 1 | a0005 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.12T>G | p.His4Gln | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/9 | 130/1119 | 12/807 | 4/268 | chr13 | 51799648 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51791174 | G | C | 1 | a0002c0010 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.210C>G | p.Leu70Leu | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 3/9 | 328/1119 | 210/807 | 70/268 | chr13 | 51791174 | |||
| chr13:51799551 | A | G | 1 | a0001c0004 | 3 | HG02486.hp1 HG03831.hp1 HG03834.hp2 |
synonymous_variant | LOW | c.109T>C | p.Leu37Leu | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/9 | 227/1119 | 109/807 | 37/268 | chr13 | 51799551 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51768070 | G | A | 8 | a0001c0001t0002 a0001c0001t0003 a0002c0002t0003 others(5): Show |
125 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*117C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 9/9 | 117 | chr13 | 51768070 | ||||||
| chr13:51768074 | CACA | C | 1 | a0003c0003t0005 | 3 | NA18979.hp2 NA18993.hp1 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*110_*112delTGT | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 9/9 | 110 | chr13 | 51768074 | ||||||
| chr13:51768105 | GTCT | G | 4 | a0001c0001t0003 a0002c0002t0003 a0002c0002t0006 others(1): Show |
61 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*79_*81delAGA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 9/9 | 79 | chr13 | 51768105 | ||||||
| chr13:51768108 | T | G | 2 | a0001c0001t0007 a0003c0003t0005 |
4 | HG01884.hp2 NA18979.hp2 NA18993.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*79A>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 9/9 | 79 | chr13 | 51768108 | ||||||
| chr13:51804117 | G | C | 1 | a0001c0001t0008 | 1 | HG03098.hp1 | 5_prime_UTR_variant | MODIFIER | c.-72C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/9 | 4458 | chr13 | 51804117 | ||||||
| chr13:51804146 | CG | C | 3 | a0001c0001t0004 a0002c0002t0006 a0007c0006t0004 |
10 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-102delC | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/9 | 4488 | chr13 | 51804146 | ||||||
| chr13:51804149 | C | T | 3 | a0001c0001t0004 a0002c0002t0006 a0007c0006t0004 |
10 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-104G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/9 | 4490 | chr13 | 51804149 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51768410 | A | G | 49 | a0001c0001t0001g0321 a0001c0001t0003g0004 a0001c0001t0003g0076 others(46): Show |
62 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(59): Show |
intron_variant | MODIFIER | c.698-114T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 8/8 | chr13 | 51768410 | |||||||
| chr13:51768533 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0206 |
2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.698-237C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 8/8 | chr13 | 51768533 | |||||||
| chr13:51768546 | GA | G | 2 | a0001c0001t0004g0007 a0001c0001t0004g0066 |
4 | HG02109.hp1 HG02280.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-251delT | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 8/8 | chr13 | 51768546 | |||||||
| chr13:51768547 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.698-251T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 8/8 | chr13 | 51768547 | |||||||
| chr13:51768548 | A | G | 5 | a0001c0001t0001g0150 a0001c0001t0001g0161 a0001c0001t0001g0177 others(2): Show |
6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.698-252T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 8/8 | chr13 | 51768548 | |||||||
| chr13:51768657 | C | G | 2 | a0003c0003t0001g0220 a0003c0003t0001g0236 |
2 | HG00323.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.698-361G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 8/8 | chr13 | 51768657 | |||||||
| chr13:51768674 | G | A | 1 | a0001c0001t0001g0008 | 3 | HG01074.hp1 HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.698-378C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 8/8 | chr13 | 51768674 | |||||||
| chr13:51768763 | A | G | 6 | a0002c0002t0003g0017 a0002c0002t0003g0190 a0002c0002t0003g0217 others(3): Show |
8 | HG01106.hp2 HG02055.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.697+393T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 8/8 | chr13 | 51768763 | |||||||
| chr13:51768787 | C | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0234 |
2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.697+369G>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 8/8 | chr13 | 51768787 | |||||||
| chr13:51768848 | C | T | 5 | a0001c0001t0001g0150 a0001c0001t0001g0161 a0001c0001t0001g0177 others(2): Show |
6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.697+308G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 8/8 | chr13 | 51768848 | |||||||
| chr13:51768868 | A | G | 49 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0020 others(46): Show |
64 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.697+288T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 8/8 | chr13 | 51768868 | |||||||
| chr13:51768877 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.697+279T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 8/8 | chr13 | 51768877 | |||||||
| chr13:51768941 | G | T | 2 | a0001c0001t0004g0007 a0001c0001t0004g0066 |
4 | HG02109.hp1 HG02280.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.697+215C>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 8/8 | chr13 | 51768941 | |||||||
| chr13:51769034 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.697+122G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 8/8 | chr13 | 51769034 | |||||||
| chr13:51769363 | T | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0160 |
2 | HG03041.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.560-70A>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51769363 | |||||||
| chr13:51769363 | T | TA | 111 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(108): Show |
147 | HG00099.hp2 HG00423.hp1 HG00735.hp1 others(144): Show |
intron_variant | MODIFIER | c.560-71dupT | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51769363 | |||||||
| chr13:51769394 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.560-101C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51769394 | |||||||
| chr13:51769408 | T | C | 1 | a0001c0001t0001g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.560-115A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51769408 | |||||||
| chr13:51769415 | A | G | 49 | a0001c0001t0003g0004 a0001c0001t0003g0259 a0001c0001t0003g0275 others(46): Show |
62 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(59): Show |
intron_variant | MODIFIER | c.560-122T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51769415 | |||||||
| chr13:51769499 | T | C | 65 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0040 others(62): Show |
81 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.560-206A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51769499 | |||||||
| chr13:51769538 | G | A | 2 | a0002c0002t0003g0042 a0002c0002t0003g0174 |
3 | HG01243.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.560-245C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51769538 | |||||||
| chr13:51769558 | A | G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0250 a0002c0002t0003g0255 |
3 | HG01123.hp1 HG01261.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.560-265T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51769558 | |||||||
| chr13:51769778 | A | C | 1 | a0001c0001t0001g0272 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.560-485T>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51769778 | |||||||
| chr13:51769806 | C | T | 3 | a0001c0001t0002g0061 a0001c0001t0002g0323 a0003c0003t0002g0248 |
4 | HG02698.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-513G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51769806 | |||||||
| chr13:51769868 | G | A | 43 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0020 others(40): Show |
58 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.560-575C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51769868 | |||||||
| chr13:51769891 | C | G | 3 | a0001c0001t0001g0325 a0001c0001t0003g0076 a0001c0001t0004g0064 |
3 | HG02451.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.560-598G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51769891 | |||||||
| chr13:51769932 | C | T | 1 | a0001c0001t0002g0124 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.560-639G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51769932 | |||||||
| chr13:51770024 | T | C | 6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.560-731A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770024 | |||||||
| chr13:51770076 | T | C | 1 | a0003c0003t0001g0239 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.560-783A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770076 | |||||||
| chr13:51770087 | T | A | 1 | a0002c0002t0003g0249 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.560-794A>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770087 | |||||||
| chr13:51770136 | T | A | 7 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(4): Show |
7 | HG01884.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.560-843A>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770136 | |||||||
| chr13:51770154 | C | G | 1 | a0001c0001t0001g0254 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.560-861G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770154 | |||||||
| chr13:51770154 | C | T | 1 | a0001c0001t0001g0302 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.560-861G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770154 | |||||||
| chr13:51770258 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0001t0001g0067 |
5 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.560-965G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770258 | |||||||
| chr13:51770301 | G | A | 1 | a0002c0002t0003g0050 | 2 | HG01081.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.560-1008C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770301 | |||||||
| chr13:51770369 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.560-1076G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770369 | |||||||
| chr13:51770736 | GGGGTGTG others(24): Show |
G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.559+1054_559+1084d others(33): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770736 | |||||||
| chr13:51770770 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.559+1051G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770770 | |||||||
| chr13:51770773 | G | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.559+1048C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770773 | |||||||
| chr13:51770775 | A | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.559+1046T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770775 | |||||||
| chr13:51770777 | T | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.559+1044A>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770777 | |||||||
| chr13:51770778 | A | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.559+1043T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770778 | |||||||
| chr13:51770781 | C | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.559+1040G>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770781 | |||||||
| chr13:51770783 | G | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.559+1038C>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770783 | |||||||
| chr13:51770860 | C | G | 1 | a0001c0001t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.559+961G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770860 | |||||||
| chr13:51770863 | T | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.559+958A>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770863 | |||||||
| chr13:51770913 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.559+908G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51770913 | |||||||
| chr13:51771091 | C | T | 1 | a0002c0002t0003g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.559+730G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51771091 | |||||||
| chr13:51771097 | T | A | 1 | a0001c0001t0001g0280 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.559+724A>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51771097 | |||||||
| chr13:51771177 | C | A | 1 | a0001c0001t0001g0024 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.559+644G>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51771177 | |||||||
| chr13:51771194 | C | T | 1 | a0002c0002t0003g0175 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.559+627G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51771194 | |||||||
| chr13:51771196 | C | T | 1 | a0003c0003t0001g0221 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.559+625G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51771196 | |||||||
| chr13:51771216 | G | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0234 |
2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.559+605C>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51771216 | |||||||
| chr13:51771324 | G | A | 4 | a0001c0001t0002g0014 a0001c0001t0002g0267 a0001c0001t0002g0285 others(1): Show |
6 | HG02015.hp2 NA18948.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.559+497C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51771324 | |||||||
| chr13:51771500 | C | T | 1 | a0002c0002t0003g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.559+321G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51771500 | |||||||
| chr13:51771501 | G | C | 50 | a0001c0001t0001g0212 a0001c0001t0002g0001 a0001c0001t0002g0014 others(47): Show |
65 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.559+320C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51771501 | |||||||
| chr13:51771645 | T | C | 60 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(57): Show |
73 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(70): Show |
intron_variant | MODIFIER | c.559+176A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51771645 | |||||||
| chr13:51771702 | T | C | 48 | a0001c0001t0003g0004 a0001c0001t0003g0259 a0001c0001t0003g0275 others(45): Show |
61 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.559+119A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51771702 | |||||||
| chr13:51771787 | G | A | 1 | a0001c0001t0001g0008 | 3 | HG01074.hp1 HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.559+34C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 7/8 | chr13 | 51771787 | |||||||
| chr13:51771928 | G | A | 2 | a0001c0001t0001g0058 a0003c0003t0001g0240 |
3 | NA18944.hp1 NA18963.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.469-17C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 6/8 | chr13 | 51771928 | |||||||
| chr13:51771930 | G | A | 1 | a0007c0006t0004g0062 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.469-19C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 6/8 | chr13 | 51771930 | |||||||
| chr13:51772039 | G | C | 1 | a0001c0001t0001g0094 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.469-128C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 6/8 | chr13 | 51772039 | |||||||
| chr13:51772097 | C | T | 1 | a0002c0002t0003g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.469-186G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 6/8 | chr13 | 51772097 | |||||||
| chr13:51772139 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.469-228G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 6/8 | chr13 | 51772139 | |||||||
| chr13:51772198 | A | G | 3 | a0001c0001t0001g0325 a0001c0001t0003g0076 a0001c0001t0004g0064 |
3 | HG02451.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.469-287T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 6/8 | chr13 | 51772198 | |||||||
| chr13:51772227 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.469-316C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 6/8 | chr13 | 51772227 | |||||||
| chr13:51772379 | A | G | 3 | a0001c0001t0001g0325 a0001c0001t0003g0076 a0001c0001t0004g0064 |
3 | HG02451.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.469-468T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 6/8 | chr13 | 51772379 | |||||||
| chr13:51772983 | G | C | 7 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(4): Show |
7 | HG01884.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+947C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 6/8 | chr13 | 51772983 | |||||||
| chr13:51773084 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.468+846A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 6/8 | chr13 | 51773084 | |||||||
| chr13:51773104 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0234 |
2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.468+826C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 6/8 | chr13 | 51773104 | |||||||
| chr13:51773207 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.468+723A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 6/8 | chr13 | 51773207 | |||||||
| chr13:51773303 | G | A | 56 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(53): Show |
69 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(66): Show |
intron_variant | MODIFIER | c.468+627C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 6/8 | chr13 | 51773303 | |||||||
| chr13:51773417 | G | A | 48 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(45): Show |
58 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.468+513C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 6/8 | chr13 | 51773417 | |||||||
| chr13:51773620 | G | A | 1 | a0001c0001t0004g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.468+310C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 6/8 | chr13 | 51773620 | |||||||
| chr13:51773700 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.468+230C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 6/8 | chr13 | 51773700 | |||||||
| chr13:51773838 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0096 others(2): Show |
8 | NA18952.hp2 NA18971.hp1 NA18972.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+92C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 6/8 | chr13 | 51773838 | |||||||
| chr13:51773890 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0113 a0006c0007t0001g0090 |
3 | HG02015.hp1 NA18979.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.468+40G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 6/8 | chr13 | 51773890 | |||||||
| chr13:51773891 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.468+39C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 6/8 | chr13 | 51773891 | |||||||
| chr13:51774056 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.364-22A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774056 | |||||||
| chr13:51774185 | C | T | 1 | a0002c0002t0003g0246 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.364-151G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774185 | |||||||
| chr13:51774190 | GTACATGT others(294): Show |
G | 7 | a0001c0001t0001g0035 a0001c0001t0001g0146 a0001c0001t0001g0147 others(4): Show |
8 | HG01192.hp2 HG01884.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.364-457_364-157del | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774190 | |||||||
| chr13:51774203 | C | T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0071 a0001c0001t0001g0077 others(2): Show |
6 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-169G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774203 | |||||||
| chr13:51774223 | GTACATGT others(20): Show |
G | 24 | a0001c0001t0003g0259 a0002c0002t0001g0193 a0002c0002t0003g0002 others(21): Show |
29 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.364-216_364-190del others(27): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774223 | |||||||
| chr13:51774241 | AGTATTCT others(7): Show |
A | 11 | a0002c0002t0003g0017 a0002c0002t0003g0072 a0002c0002t0003g0157 others(8): Show |
13 | HG01261.hp2 HG02055.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.364-221_364-208del others(14): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774241 | |||||||
| chr13:51774254 | AT | A | 9 | a0002c0002t0003g0042 a0002c0002t0003g0044 a0002c0002t0003g0049 others(6): Show |
9 | HG01255.hp2 HG01934.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.364-221delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774254 | |||||||
| chr13:51774255 | TGTATTCT others(6): Show |
T | 60 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(57): Show |
79 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.364-234_364-222del others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774255 | |||||||
| chr13:51774281 | A | AT | 3 | a0001c0001t0001g0127 a0001c0001t0001g0321 a0002c0002t0003g0158 |
3 | HG01255.hp2 HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.364-248_364-247ins others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774281 | |||||||
| chr13:51774294 | AT | A | 32 | a0001c0001t0003g0259 a0002c0002t0001g0193 a0002c0002t0003g0002 others(29): Show |
39 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.364-261delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774294 | |||||||
| chr13:51774349 | T | TGTATTCT others(241): Show |
1 | a0001c0001t0001g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.364-316_364-315ins others(248): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774349 | |||||||
| chr13:51774349 | TGTATTCT others(543): Show |
T | 1 | a0001c0001t0001g0166 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.364-865_364-316del | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774349 | |||||||
| chr13:51774354 | TCTC | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0321 a0002c0002t0001g0191 |
3 | HG02559.hp2 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.364-323_364-321del others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774354 | |||||||
| chr13:51774362 | A | AT | 5 | a0002c0002t0003g0074 a0002c0002t0003g0157 a0002c0002t0003g0246 others(2): Show |
5 | HG01934.hp1 HG01978.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-329_364-328ins others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774362 | |||||||
| chr13:51774362 | AGTATTCT others(99): Show |
A | 6 | a0002c0002t0003g0042 a0002c0002t0003g0044 a0002c0002t0003g0049 others(3): Show |
6 | HG01261.hp2 HG02145.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-434_364-329del | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774362 | |||||||
| chr13:51774375 | ATGTATTC others(114): Show |
A | 5 | a0002c0002t0003g0074 a0002c0002t0003g0157 a0002c0002t0003g0246 others(2): Show |
5 | HG01934.hp1 HG01978.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-462_364-342del | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774375 | |||||||
| chr13:51774376 | TGTATTCT others(86): Show |
T | 19 | a0001c0001t0003g0259 a0002c0002t0001g0193 a0002c0002t0003g0002 others(16): Show |
24 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.364-435_364-343del others(93): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774376 | |||||||
| chr13:51774376 | TGTATTCT others(126): Show |
T | 1 | a0001c0001t0007g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.364-475_364-343del | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774376 | |||||||
| chr13:51774376 | TGTATTCT others(163): Show |
T | 4 | a0002c0002t0003g0154 a0002c0002t0003g0175 a0002c0002t0003g0189 others(1): Show |
4 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-512_364-343del | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774376 | |||||||
| chr13:51774376 | TGTATTCT others(241): Show |
T | 1 | a0001c0001t0001g0128 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.364-590_364-343del | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774376 | |||||||
| chr13:51774376 | TGTATTCT others(438): Show |
T | 1 | a0002c0002t0003g0232 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.364-787_364-343del | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774376 | |||||||
| chr13:51774381 | T | TCTC | 7 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(4): Show |
7 | HG01255.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-348_364-347ins others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774381 | |||||||
| chr13:51774399 | ATGTATTC others(31): Show |
A | 1 | a0002c0002t0001g0191 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.364-403_364-366del others(38): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774399 | |||||||
| chr13:51774400 | TGTATTCT others(3): Show |
T | 8 | a0002c0002t0003g0017 a0002c0002t0003g0176 a0002c0002t0003g0190 others(5): Show |
10 | HG01106.hp2 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.364-376_364-367del others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774400 | |||||||
| chr13:51774418 | C | CCTACATG others(244): Show |
6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-385_364-384ins others(251): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774418 | |||||||
| chr13:51774423 | AGTATTCT others(193): Show |
A | 1 | a0002c0002t0003g0158 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.364-589_364-390del | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774423 | |||||||
| chr13:51774431 | CCTACATG others(268): Show |
C | 69 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0015 others(66): Show |
97 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.364-672_364-398del | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774431 | |||||||
| chr13:51774431 | CCTACATG others(818): Show |
C | 3 | a0001c0001t0001g0256 a0003c0003t0001g0045 a0003c0003t0001g0235 |
4 | HG00099.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-1222_364-398de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774431 | |||||||
| chr13:51774442 | TCTCCTAC others(68): Show |
T | 1 | a0002c0002t0003g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.364-483_364-409del others(75): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774442 | |||||||
| chr13:51774443 | CTCCTACA others(1): Show |
C | 7 | a0002c0002t0003g0017 a0002c0002t0003g0190 a0002c0002t0003g0217 others(4): Show |
9 | HG01106.hp2 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.364-417_364-410del others(8): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774443 | |||||||
| chr13:51774451 | G | GTATTCTC others(1): Show |
6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-418_364-417ins others(8): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774451 | |||||||
| chr13:51774451 | G | GTATTCTC others(15): Show |
2 | a0001c0001t0001g0127 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.364-418_364-417ins others(22): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774451 | |||||||
| chr13:51774455 | AT | A | 7 | a0002c0002t0003g0017 a0002c0002t0003g0190 a0002c0002t0003g0217 others(4): Show |
9 | HG01106.hp2 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.364-422delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774455 | |||||||
| chr13:51774469 | A | AT | 7 | a0002c0002t0003g0017 a0002c0002t0003g0190 a0002c0002t0003g0217 others(4): Show |
9 | HG01106.hp2 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.364-436_364-435ins others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774469 | |||||||
| chr13:51774469 | A | T | 6 | a0002c0002t0003g0042 a0002c0002t0003g0044 a0002c0002t0003g0049 others(3): Show |
6 | HG01261.hp2 HG02145.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-435T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774469 | |||||||
| chr13:51774474 | TCTC | T | 7 | a0002c0002t0003g0017 a0002c0002t0003g0190 a0002c0002t0003g0217 others(4): Show |
9 | HG01106.hp2 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.364-443_364-441del others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774474 | |||||||
| chr13:51774477 | C | CCTACATG others(4): Show |
6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-444_364-443ins others(11): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774477 | |||||||
| chr13:51774482 | A | AT | 19 | a0001c0001t0003g0259 a0002c0002t0001g0193 a0002c0002t0003g0002 others(16): Show |
24 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.364-449_364-448ins others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774482 | |||||||
| chr13:51774495 | AT | A | 19 | a0001c0001t0003g0259 a0002c0002t0001g0193 a0002c0002t0003g0002 others(16): Show |
24 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.364-462delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774495 | |||||||
| chr13:51774496 | TGTATTCT others(6): Show |
T | 13 | a0002c0002t0003g0017 a0002c0002t0003g0042 a0002c0002t0003g0044 others(10): Show |
15 | HG01106.hp2 HG01261.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.364-475_364-463del others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774496 | |||||||
| chr13:51774501 | TCTCCTAC others(9): Show |
T | 1 | a0001c0001t0002g0043 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.364-483_364-468del others(16): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774501 | |||||||
| chr13:51774509 | A | AT | 24 | a0001c0001t0003g0259 a0002c0002t0001g0193 a0002c0002t0003g0002 others(21): Show |
29 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.364-476_364-475ins others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774509 | |||||||
| chr13:51774517 | C | CCTACAGT others(17): Show |
8 | a0001c0001t0001g0152 a0001c0001t0001g0164 a0001c0001t0001g0271 others(5): Show |
8 | HG00558.hp2 NA18945.hp1 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-507_364-484dup others(24): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774517 | |||||||
| chr13:51774517 | C | CCTACATG others(100): Show |
5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(2): Show |
5 | HG02818.hp1 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-484_364-483ins others(107): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774517 | |||||||
| chr13:51774517 | C | CCTACATG others(124): Show |
1 | a0001c0001t0001g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.364-484_364-483ins others(131): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774517 | |||||||
| chr13:51774546 | AGTATTCT others(7): Show |
A | 1 | a0002c0002t0003g0249 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.364-526_364-513del others(14): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774546 | |||||||
| chr13:51774546 | AGTATTCT others(282): Show |
A | 1 | a0001c0001t0001g0263 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.364-801_364-513del | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774546 | |||||||
| chr13:51774560 | T | TGTATTCT others(3): Show |
7 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(4): Show |
7 | HG02559.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-527_364-526ins others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774560 | |||||||
| chr13:51774560 | TGTATTCT others(57): Show |
T | 26 | a0001c0001t0003g0259 a0002c0002t0001g0193 a0002c0002t0003g0002 others(23): Show |
33 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.364-590_364-527del others(64): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774560 | |||||||
| chr13:51774560 | TGTATTCT others(217): Show |
T | 1 | a0002c0002t0003g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.364-750_364-527del | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774560 | |||||||
| chr13:51774565 | TCTCCTAC others(1293): Show |
T | 1 | a0001c0001t0002g0043 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.363+1195_364-532de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774565 | |||||||
| chr13:51774573 | AT | A | 14 | a0001c0001t0001g0127 a0001c0001t0007g0156 a0002c0002t0003g0017 others(11): Show |
16 | HG01884.hp2 HG01891.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.364-540delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774573 | |||||||
| chr13:51774574 | TGTATTCT others(43): Show |
T | 1 | a0002c0002t0003g0249 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.364-590_364-541del others(50): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774574 | |||||||
| chr13:51774582 | CCTACAGT others(30): Show |
C | 1 | a0003c0003t0001g0223 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.364-585_364-549del others(37): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774582 | |||||||
| chr13:51774587 | A | AGTATTCT others(7): Show |
6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-554_364-553ins others(14): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774587 | |||||||
| chr13:51774587 | A | AT | 14 | a0001c0001t0001g0127 a0001c0001t0007g0156 a0002c0002t0003g0017 others(11): Show |
16 | HG01884.hp2 HG01891.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.364-554_364-553ins others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774587 | |||||||
| chr13:51774592 | T | A | 1 | a0001c0001t0001g0094 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.364-558A>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774592 | |||||||
| chr13:51774592 | TCTC | T | 7 | a0001c0001t0001g0127 a0001c0001t0007g0156 a0002c0002t0003g0017 others(4): Show |
9 | HG01884.hp2 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.364-561_364-559del others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774592 | |||||||
| chr13:51774592 | TCTCCTAC others(33): Show |
T | 3 | a0002c0002t0003g0044 a0002c0002t0003g0073 a0002c0002t0003g0209 |
3 | HG01891.hp1 HG02004.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.364-598_364-559del others(40): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774592 | |||||||
| chr13:51774595 | C | CCTACATG others(52): Show |
1 | a0001c0001t0001g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.364-562_364-561ins others(59): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774595 | |||||||
| chr13:51774595 | CCTACAGT others(17): Show |
C | 1 | a0001c0001t0001g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.364-585_364-562del others(24): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774595 | |||||||
| chr13:51774608 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.364-574G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774608 | |||||||
| chr13:51774614 | TGTATTCT others(3): Show |
T | 1 | a0002c0002t0003g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.364-590_364-581del others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774614 | |||||||
| chr13:51774619 | T | TCTCCTAC others(122): Show |
1 | a0001c0001t0001g0033 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.364-586_364-585ins others(129): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774619 | |||||||
| chr13:51774619 | TCTACAGT others(6): Show |
T | 4 | a0001c0001t0002g0059 a0001c0001t0002g0183 a0001c0001t0002g0278 others(1): Show |
5 | HG01884.hp2 NA18964.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-598_364-586del others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774619 | |||||||
| chr13:51774624 | A | T | 1 | a0002c0002t0003g0158 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.364-590T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774624 | |||||||
| chr13:51774632 | C | CCTACATG others(4): Show |
8 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0130 others(5): Show |
8 | HG02559.hp2 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.364-599_364-598ins others(11): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774632 | |||||||
| chr13:51774637 | A | AT | 4 | a0002c0002t0003g0017 a0002c0002t0003g0190 a0002c0002t0003g0247 others(1): Show |
6 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.364-604_364-603ins others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774637 | |||||||
| chr13:51774637 | AGTATTCT others(139): Show |
A | 4 | a0002c0002t0003g0154 a0002c0002t0003g0175 a0002c0002t0003g0189 others(1): Show |
4 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-749_364-604del | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774637 | |||||||
| chr13:51774645 | CCTACATG others(4): Show |
C | 4 | a0002c0002t0003g0017 a0002c0002t0003g0190 a0002c0002t0003g0247 others(1): Show |
6 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.364-622_364-612del others(11): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774645 | |||||||
| chr13:51774675 | TGTATTCT others(102): Show |
T | 2 | a0002c0002t0003g0044 a0002c0002t0003g0073 |
2 | HG01891.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.364-750_364-642del | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774675 | |||||||
| chr13:51774680 | TCTACAGT others(65): Show |
T | 12 | a0002c0002t0003g0002 a0002c0002t0003g0042 a0002c0002t0003g0044 others(9): Show |
16 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.364-718_364-647del others(72): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774680 | |||||||
| chr13:51774680 | TCTACAGT others(1165): Show |
T | 2 | a0001c0001t0003g0076 a0001c0001t0004g0064 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.363+1208_364-647de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774680 | |||||||
| chr13:51774693 | C | CCTACATG others(4): Show |
1 | a0001c0001t0001g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.364-660_364-659ins others(11): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774693 | |||||||
| chr13:51774693 | C | CCTACATG others(31): Show |
6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-660_364-659ins others(38): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774693 | |||||||
| chr13:51774693 | CCTACAGT others(1422): Show |
C | 1 | a0001c0001t0001g0092 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.363+938_364-660del | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774693 | |||||||
| chr13:51774694 | CTACAGTA others(25): Show |
C | 6 | a0001c0001t0003g0259 a0002c0002t0001g0193 a0002c0002t0003g0159 others(3): Show |
6 | HG00735.hp1 HG01106.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.364-692_364-661del others(32): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774694 | |||||||
| chr13:51774698 | A | AT | 10 | a0001c0001t0001g0321 a0001c0001t0007g0156 a0002c0002t0003g0017 others(7): Show |
10 | HG01884.hp2 HG01934.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.364-665_364-664ins others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774698 | |||||||
| chr13:51774698 | AGTATTCT others(51): Show |
A | 3 | a0002c0002t0003g0017 a0002c0002t0003g0190 a0002c0002t0003g0247 |
4 | HG02486.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-722_364-665del others(58): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774698 | |||||||
| chr13:51774698 | AGTATTCT others(78): Show |
A | 7 | a0002c0002t0003g0002 a0002c0002t0003g0049 a0002c0002t0003g0050 others(4): Show |
8 | HG01081.hp2 HG01109.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.364-749_364-665del others(85): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774698 | |||||||
| chr13:51774698 | AGTATTCT others(353): Show |
A | 1 | a0002c0002t0003g0209 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.364-1024_364-665de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774698 | |||||||
| chr13:51774698 | AGTATTCT others(1436): Show |
A | 1 | a0001c0001t0002g0303 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.363+919_364-665del | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774698 | |||||||
| chr13:51774703 | TCTACTAC others(42): Show |
T | 1 | a0001c0001t0007g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.364-718_364-670del others(49): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774703 | |||||||
| chr13:51774706 | A | C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(187): Show |
236 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.364-672T>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774706 | |||||||
| chr13:51774707 | CTACATGT others(12): Show |
C | 1 | a0003c0003t0001g0221 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.364-692_364-674del others(19): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774707 | |||||||
| chr13:51774711 | AT | A | 8 | a0002c0002t0003g0017 a0002c0002t0003g0072 a0002c0002t0003g0074 others(5): Show |
8 | HG01934.hp1 HG01978.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.364-678delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774711 | |||||||
| chr13:51774712 | T | A | 1 | a0001c0001t0001g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.364-678A>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774712 | |||||||
| chr13:51774717 | TCTCCTAC others(1141): Show |
T | 1 | a0001c0001t0001g0325 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.363+1195_364-684de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774717 | |||||||
| chr13:51774721 | CTACAG | C | 8 | a0002c0002t0003g0017 a0002c0002t0003g0072 a0002c0002t0003g0074 others(5): Show |
8 | HG01934.hp1 HG01978.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.364-692_364-688del others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774721 | |||||||
| chr13:51774726 | G | C | 1 | a0001c0001t0001g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.364-692C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774726 | |||||||
| chr13:51774726 | G | GTATTCTC others(1): Show |
7 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0130 others(4): Show |
7 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-693_364-692ins others(8): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774726 | |||||||
| chr13:51774731 | TGTATTCT others(6): Show |
T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0086 a0001c0001t0001g0148 others(2): Show |
7 | HG00621.hp2 HG02135.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-710_364-698del others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774731 | |||||||
| chr13:51774731 | TGTATTCT others(46): Show |
T | 1 | a0002c0002t0003g0249 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.364-750_364-698del others(53): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774731 | |||||||
| chr13:51774736 | TCTC | T | 7 | a0001c0001t0001g0127 a0002c0002t0003g0072 a0002c0002t0003g0074 others(4): Show |
7 | HG01934.hp1 HG01978.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-705_364-703del others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774736 | |||||||
| chr13:51774744 | A | G | 1 | a0001c0001t0001g0257 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.364-710T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774744 | |||||||
| chr13:51774745 | G | A | 6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-711C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774745 | |||||||
| chr13:51774752 | C | CCTACATG others(4): Show |
6 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.364-719_364-718ins others(11): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774752 | |||||||
| chr13:51774757 | A | AT | 12 | a0001c0001t0003g0259 a0002c0002t0001g0193 a0002c0002t0003g0017 others(9): Show |
12 | HG00735.hp1 HG01934.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.364-724_364-723ins others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774757 | |||||||
| chr13:51774757 | A | ATGTATTC others(171): Show |
1 | a0001c0001t0001g0130 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.364-724_364-723ins others(178): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774757 | |||||||
| chr13:51774757 | A | T | 3 | a0002c0002t0003g0017 a0002c0002t0003g0190 a0002c0002t0003g0247 |
4 | HG02486.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-723T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774757 | |||||||
| chr13:51774757 | AGTATTCT others(7): Show |
A | 1 | a0001c0001t0002g0214 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.364-737_364-724del others(14): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774757 | |||||||
| chr13:51774762 | TCTC | T | 6 | a0001c0001t0003g0259 a0002c0002t0001g0193 a0002c0002t0003g0017 others(3): Show |
6 | HG00735.hp1 HG01975.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.364-731_364-729del others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774762 | |||||||
| chr13:51774769 | C | T | 3 | a0001c0001t0001g0163 a0001c0001t0001g0215 a0001c0001t0001g0250 |
3 | HG01123.hp1 HG01515.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.364-735G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774769 | |||||||
| chr13:51774770 | AT | A | 17 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0003g0259 others(14): Show |
19 | HG00735.hp1 HG01934.hp1 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.364-737delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774770 | |||||||
| chr13:51774771 | TGTATTCT others(6): Show |
T | 15 | a0001c0001t0001g0215 a0002c0002t0003g0002 a0002c0002t0003g0042 others(12): Show |
19 | HG00597.hp1 HG01106.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.364-750_364-738del others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774771 | |||||||
| chr13:51774775 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.364-741A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774775 | |||||||
| chr13:51774776 | TCTCCTAC others(9): Show |
T | 1 | a0001c0001t0007g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.364-758_364-743del others(16): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774776 | |||||||
| chr13:51774784 | A | AGTATTCT others(82): Show |
5 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-751_364-750ins others(89): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774784 | |||||||
| chr13:51774784 | A | AT | 17 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0003g0259 others(14): Show |
19 | HG00735.hp1 HG01934.hp1 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.364-751_364-750ins others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774784 | |||||||
| chr13:51774784 | A | T | 11 | a0002c0002t0003g0002 a0002c0002t0003g0049 a0002c0002t0003g0050 others(8): Show |
12 | HG01081.hp2 HG01109.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.364-750T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774784 | |||||||
| chr13:51774789 | TCTC | T | 8 | a0001c0001t0001g0127 a0001c0001t0003g0296 a0002c0002t0003g0072 others(5): Show |
8 | HG01934.hp1 HG01978.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-758_364-756del others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774789 | |||||||
| chr13:51774792 | C | CCTACATG others(4): Show |
1 | a0001c0001t0001g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.364-759_364-758ins others(11): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774792 | |||||||
| chr13:51774821 | AGTATTCT others(7): Show |
A | 1 | a0001c0001t0001g0179 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.364-801_364-788del others(14): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774821 | |||||||
| chr13:51774835 | TGTATTCT others(20): Show |
T | 3 | a0002c0002t0003g0017 a0002c0002t0003g0190 a0002c0002t0003g0247 |
4 | HG02486.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-828_364-802del others(27): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774835 | |||||||
| chr13:51774835 | TGTATTCT others(57): Show |
T | 6 | a0002c0002t0003g0072 a0002c0002t0003g0074 a0002c0002t0003g0244 others(3): Show |
6 | HG01934.hp1 HG01978.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-865_364-802del others(64): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774835 | |||||||
| chr13:51774839 | T | C | 1 | a0001c0001t0003g0296 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.364-805A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774839 | |||||||
| chr13:51774840 | TCTC | T | 15 | a0001c0001t0001g0127 a0001c0001t0001g0321 a0001c0001t0003g0259 others(12): Show |
15 | HG00735.hp1 HG01884.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.364-809_364-807del others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774840 | |||||||
| chr13:51774840 | TCTCCTAC others(455): Show |
T | 1 | a0001c0001t0003g0296 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.364-1268_364-807de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774840 | |||||||
| chr13:51774848 | AT | A | 41 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0130 others(38): Show |
49 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.364-815delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774848 | |||||||
| chr13:51774857 | CCTACAGT others(30): Show |
C | 2 | a0001c0001t0002g0300 a0003c0003t0001g0223 |
2 | HG01975.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.364-860_364-824del others(37): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774857 | |||||||
| chr13:51774858 | CTACAG | C | 2 | a0003c0003t0001g0046 a0003c0003t0001g0327 |
3 | HG03492.hp1 HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.364-829_364-825del others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774858 | |||||||
| chr13:51774862 | A | AT | 41 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0130 others(38): Show |
49 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.364-829_364-828ins others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774862 | |||||||
| chr13:51774867 | TCTC | T | 22 | a0001c0001t0001g0127 a0001c0001t0001g0321 a0001c0001t0007g0156 others(19): Show |
30 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.364-836_364-834del others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774867 | |||||||
| chr13:51774870 | CCTACAGT others(604): Show |
C | 18 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0096 others(15): Show |
23 | HG01192.hp2 HG01256.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.364-1447_364-837de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774870 | |||||||
| chr13:51774889 | TGTATTCT others(3): Show |
T | 2 | a0002c0002t0003g0017 a0002c0002t0006g0063 |
2 | HG02055.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.364-865_364-856del others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774889 | |||||||
| chr13:51774894 | TCTACAGT others(6): Show |
T | 6 | a0002c0002t0003g0017 a0002c0002t0003g0189 a0002c0002t0003g0190 others(3): Show |
7 | HG02486.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-873_364-861del others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774894 | |||||||
| chr13:51774899 | A | AGTATTCT others(34): Show |
3 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0133 |
3 | HG02818.hp1 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.364-866_364-865ins others(41): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774899 | |||||||
| chr13:51774907 | C | CCTACATG others(4): Show |
4 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0321 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-874_364-873ins others(11): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774907 | |||||||
| chr13:51774907 | C | CCTACATG others(58): Show |
2 | a0001c0001t0001g0132 a0001c0001t0001g0134 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.364-874_364-873ins others(65): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774907 | |||||||
| chr13:51774912 | A | AT | 17 | a0002c0002t0003g0002 a0002c0002t0003g0042 a0002c0002t0003g0044 others(14): Show |
25 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.364-879_364-878ins others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774912 | |||||||
| chr13:51774912 | AGTATTCT others(40): Show |
A | 1 | a0001c0001t0003g0259 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.364-925_364-879del others(47): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774912 | |||||||
| chr13:51774912 | AGTATTCT others(99): Show |
A | 2 | a0002c0002t0001g0193 a0002c0002t0003g0159 |
2 | HG01975.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.364-984_364-879del | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774912 | |||||||
| chr13:51774912 | AGTATTCT others(139): Show |
A | 3 | a0002c0002t0003g0176 a0002c0002t0003g0232 a0002c0002t0003g0249 |
3 | HG01106.hp2 HG01361.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.364-1024_364-879de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774912 | |||||||
| chr13:51774912 | AGTATTCT others(254): Show |
A | 4 | a0002c0002t0003g0154 a0002c0002t0003g0175 a0002c0002t0003g0192 others(1): Show |
4 | HG02258.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-1139_364-879de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774912 | |||||||
| chr13:51774920 | CCTACATG others(4): Show |
C | 17 | a0002c0002t0003g0002 a0002c0002t0003g0042 a0002c0002t0003g0044 others(14): Show |
25 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.364-897_364-887del others(11): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774920 | |||||||
| chr13:51774920 | CCTACATG others(329): Show |
C | 2 | a0001c0001t0002g0214 a0002c0002t0001g0191 |
2 | HG01346.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.364-1222_364-887de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774920 | |||||||
| chr13:51774950 | TGTATTCT others(3): Show |
T | 1 | a0002c0002t0003g0189 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.364-926_364-917del others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774950 | |||||||
| chr13:51774950 | TGTATTCT others(62): Show |
T | 6 | a0002c0002t0003g0072 a0002c0002t0003g0074 a0002c0002t0003g0244 others(3): Show |
6 | HG01934.hp1 HG01978.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-985_364-917del others(69): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774950 | |||||||
| chr13:51774955 | TCTACAGT others(6): Show |
T | 1 | a0001c0001t0007g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.364-934_364-922del others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774955 | |||||||
| chr13:51774960 | A | AGTATTCT others(7): Show |
1 | a0001c0001t0001g0130 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.364-927_364-926ins others(14): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774960 | |||||||
| chr13:51774960 | A | T | 1 | a0001c0001t0003g0259 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.364-926T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774960 | |||||||
| chr13:51774968 | C | CCTACATG others(4): Show |
2 | a0001c0001t0001g0132 a0001c0001t0001g0134 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.364-935_364-934ins others(11): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774968 | |||||||
| chr13:51774968 | C | CCTACATG others(31): Show |
2 | a0001c0001t0001g0129 a0001c0001t0001g0133 |
2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.364-935_364-934ins others(38): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774968 | |||||||
| chr13:51774973 | A | AT | 9 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0001g0321 others(6): Show |
11 | HG01081.hp2 HG01109.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.364-940_364-939ins others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774973 | |||||||
| chr13:51774973 | AGTATTCT others(38): Show |
A | 12 | a0002c0002t0003g0002 a0002c0002t0003g0042 a0002c0002t0003g0044 others(9): Show |
18 | HG01106.hp1 HG01243.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.364-984_364-940del others(45): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774973 | |||||||
| chr13:51774973 | AGTATTCT others(78): Show |
A | 5 | a0002c0002t0003g0017 a0002c0002t0003g0190 a0002c0002t0003g0217 others(2): Show |
6 | HG02486.hp2 HG02559.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.364-1024_364-940de others(86): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774973 | |||||||
| chr13:51774973 | AGTATTCT others(193): Show |
A | 1 | a0002c0002t0003g0017 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.364-1139_364-940de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774973 | |||||||
| chr13:51774981 | C | A | 45 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0030 others(42): Show |
59 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.364-947G>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774981 | |||||||
| chr13:51774981 | CCTACATG others(268): Show |
C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0148 a0001c0001t0001g0184 others(1): Show |
6 | HG00621.hp2 HG02135.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.364-1222_364-948de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774981 | |||||||
| chr13:51774986 | AT | A | 9 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0001g0321 others(6): Show |
11 | HG01081.hp2 HG01109.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.364-953delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774986 | |||||||
| chr13:51774996 | CTACAG | C | 7 | a0001c0001t0001g0127 a0002c0002t0003g0049 a0002c0002t0003g0050 others(4): Show |
9 | HG01081.hp2 HG01109.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.364-967_364-963del others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51774996 | |||||||
| chr13:51775001 | G | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.364-967C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775001 | |||||||
| chr13:51775001 | G | GTATTCTC others(1): Show |
5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0132 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-968_364-967ins others(8): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775001 | |||||||
| chr13:51775005 | AT | A | 3 | a0001c0001t0001g0131 a0001c0001t0001g0321 a0002c0002t0003g0189 |
3 | HG02559.hp2 HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.364-972delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775005 | |||||||
| chr13:51775006 | T | TGTATTCT others(3): Show |
1 | a0001c0001t0001g0130 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.364-973_364-972ins others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775006 | |||||||
| chr13:51775006 | TGTATTCT others(6): Show |
T | 1 | a0001c0001t0004g0007 | 3 | HG02109.hp1 HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.364-985_364-973del others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775006 | |||||||
| chr13:51775019 | A | AT | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0321 others(3): Show |
6 | HG00735.hp1 HG01884.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-986_364-985ins others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775019 | |||||||
| chr13:51775019 | A | T | 14 | a0002c0002t0001g0193 a0002c0002t0003g0002 a0002c0002t0003g0042 others(11): Show |
20 | HG01106.hp1 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.364-985T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775019 | |||||||
| chr13:51775019 | AGTATTCT others(20): Show |
A | 4 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | NA18950.hp2 NA18982.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-1012_364-986de others(28): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775019 | |||||||
| chr13:51775027 | C | CCTACATG others(4): Show |
2 | a0001c0001t0001g0129 a0001c0001t0001g0133 |
2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.364-994_364-993ins others(11): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775027 | |||||||
| chr13:51775032 | A | AGTATTCT others(71): Show |
4 | a0001c0001t0001g0030 a0001c0001t0001g0139 a0001c0001t0001g0152 others(1): Show |
5 | NA18945.hp1 NA18988.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-1076_364-999du others(79): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775032 | |||||||
| chr13:51775032 | A | AT | 7 | a0001c0001t0001g0127 a0002c0002t0003g0049 a0002c0002t0003g0050 others(4): Show |
9 | HG01081.hp2 HG01109.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.364-999_364-998ins others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775032 | |||||||
| chr13:51775032 | A | ATGTATTC others(249): Show |
2 | a0001c0001t0001g0132 a0001c0001t0001g0134 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.364-999_364-998ins others(256): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775032 | |||||||
| chr13:51775032 | AGTATTCT others(7): Show |
A | 43 | a0001c0001t0002g0020 a0001c0001t0002g0053 a0001c0001t0002g0056 others(40): Show |
49 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.364-1012_364-999de others(15): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775032 | |||||||
| chr13:51775037 | TCTC | T | 7 | a0001c0001t0001g0127 a0002c0002t0003g0049 a0002c0002t0003g0050 others(4): Show |
9 | HG01081.hp2 HG01109.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.364-1006_364-1004d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775037 | |||||||
| chr13:51775045 | AT | A | 9 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0134 others(6): Show |
11 | HG01081.hp2 HG01109.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.364-1012delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775045 | |||||||
| chr13:51775046 | TGTATTCT others(6): Show |
T | 24 | a0001c0001t0001g0011 a0001c0001t0001g0106 a0001c0001t0003g0259 others(21): Show |
32 | HG00735.hp1 HG01069.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.364-1025_364-1013d others(15): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775046 | |||||||
| chr13:51775052 | C | G | 1 | a0001c0001t0001g0234 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.364-1018G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775052 | |||||||
| chr13:51775059 | A | AGTATTCT others(7): Show |
2 | a0001c0001t0001g0129 a0001c0001t0001g0133 |
2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.364-1026_364-1025i others(16): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775059 | |||||||
| chr13:51775059 | A | AGTATTCT others(211): Show |
1 | a0001c0001t0001g0130 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.364-1026_364-1025i others(220): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775059 | |||||||
| chr13:51775059 | A | AT | 9 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0134 others(6): Show |
11 | HG01081.hp2 HG01109.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.364-1026_364-1025i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775059 | |||||||
| chr13:51775059 | A | T | 9 | a0002c0002t0003g0017 a0002c0002t0003g0176 a0002c0002t0003g0190 others(6): Show |
10 | HG01106.hp2 HG01361.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.364-1025T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775059 | |||||||
| chr13:51775059 | AGTATTCT others(255): Show |
A | 1 | a0006c0007t0001g0090 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.364-1287_364-1026d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775059 | |||||||
| chr13:51775067 | C | CCTACATG others(4): Show |
1 | a0001c0001t0001g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.364-1034_364-1033i others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775067 | |||||||
| chr13:51775067 | C | CCTACATG others(82): Show |
1 | a0001c0001t0001g0131 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.364-1034_364-1033i others(91): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775067 | |||||||
| chr13:51775072 | AGTATTCT others(31): Show |
A | 1 | a0001c0001t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.364-1076_364-1039d others(40): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775072 | |||||||
| chr13:51775080 | CCTACATG others(4): Show |
C | 1 | a0001c0001t0007g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.364-1057_364-1047d others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775080 | |||||||
| chr13:51775091 | T | TCTCCTAC others(46): Show |
1 | a0001c0001t0001g0234 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.364-1058_364-1057i others(55): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775091 | |||||||
| chr13:51775110 | T | TGTATTCT others(3): Show |
2 | a0001c0001t0001g0129 a0001c0001t0001g0133 |
2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.364-1077_364-1076i others(12): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775110 | |||||||
| chr13:51775110 | TGTATTCT others(57): Show |
T | 1 | a0002c0002t0003g0209 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.364-1140_364-1077d others(66): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775110 | |||||||
| chr13:51775110 | TGTATTCT others(190): Show |
T | 16 | a0001c0001t0001g0264 a0001c0001t0001g0271 a0001c0001t0001g0272 others(13): Show |
19 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.364-1273_364-1077d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775110 | |||||||
| chr13:51775115 | TCTC | T | 16 | a0001c0001t0001g0127 a0001c0001t0001g0321 a0001c0001t0003g0259 others(13): Show |
19 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.364-1084_364-1082d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775115 | |||||||
| chr13:51775115 | TCTCCTAC others(23): Show |
T | 1 | a0002c0002t0003g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.364-1111_364-1082d others(32): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775115 | |||||||
| chr13:51775123 | AT | A | 43 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0131 others(40): Show |
52 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.364-1090delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775123 | |||||||
| chr13:51775124 | TGTATTCT others(6): Show |
T | 1 | a0001c0001t0001g0143 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.364-1103_364-1091d others(15): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775124 | |||||||
| chr13:51775124 | TGTATTCT others(203): Show |
T | 1 | a0001c0001t0001g0258 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.364-1300_364-1091d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775124 | |||||||
| chr13:51775132 | CCTACAGT others(30): Show |
C | 1 | a0003c0003t0001g0223 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.364-1135_364-1099d others(39): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775132 | |||||||
| chr13:51775132 | CCTACAGT others(67): Show |
C | 1 | a0004c0008t0002g0270 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.364-1172_364-1099d others(76): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775132 | |||||||
| chr13:51775133 | CTACAG | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0098 a0001c0001t0001g0099 others(3): Show |
8 | HG00738.hp1 HG01168.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-1104_364-1100d others(7): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775133 | |||||||
| chr13:51775137 | A | AT | 41 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0132 others(38): Show |
50 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.364-1104_364-1103i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775137 | |||||||
| chr13:51775137 | A | ATGTATTC others(201): Show |
1 | a0001c0001t0001g0131 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.364-1104_364-1103i others(210): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775137 | |||||||
| chr13:51775142 | TCTC | T | 32 | a0001c0001t0001g0127 a0001c0001t0001g0321 a0001c0001t0003g0259 others(29): Show |
40 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.364-1111_364-1109d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775142 | |||||||
| chr13:51775145 | C | CCTACATG others(4): Show |
2 | a0001c0001t0001g0129 a0001c0001t0001g0133 |
2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.364-1112_364-1111i others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775145 | |||||||
| chr13:51775145 | CCTACAGT others(329): Show |
C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(38): Show |
57 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.364-1447_364-1112d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775145 | |||||||
| chr13:51775145 | CCTACAGT others(604): Show |
C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0215 |
2 | HG01123.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.363+1304_364-1112d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775145 | |||||||
| chr13:51775164 | TGTATTCT others(3): Show |
T | 9 | a0001c0001t0003g0259 a0002c0002t0003g0049 a0002c0002t0003g0050 others(6): Show |
11 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.364-1140_364-1131d others(12): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775164 | |||||||
| chr13:51775169 | T | TCTCCTAC others(243): Show |
2 | a0001c0001t0001g0129 a0001c0001t0001g0133 |
2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.364-1136_364-1135i others(252): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775169 | |||||||
| chr13:51775169 | TCTACAGT others(6): Show |
T | 26 | a0001c0001t0007g0156 a0002c0002t0001g0193 a0002c0002t0003g0002 others(23): Show |
33 | HG01106.hp1 HG01243.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.364-1148_364-1136d others(15): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775169 | |||||||
| chr13:51775169 | TCTACAGT others(342): Show |
T | 2 | a0001c0001t0004g0007 a0001c0001t0004g0066 |
4 | HG02109.hp1 HG02280.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-1484_364-1136d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775169 | |||||||
| chr13:51775174 | A | AGTATTCT others(34): Show |
4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG02630.hp1 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-1141_364-1140i others(43): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775174 | |||||||
| chr13:51775174 | A | AT | 3 | a0001c0001t0001g0129 a0001c0001t0001g0133 a0001c0001t0001g0234 |
3 | HG02717.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.364-1141_364-1140i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775174 | |||||||
| chr13:51775174 | A | T | 5 | a0002c0002t0003g0017 a0002c0002t0003g0154 a0002c0002t0003g0175 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-1140T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775174 | |||||||
| chr13:51775182 | C | CCTACATG others(4): Show |
2 | a0001c0001t0001g0127 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.364-1149_364-1148i others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775182 | |||||||
| chr13:51775187 | AGTATTCT others(254): Show |
A | 1 | a0002c0002t0003g0232 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.364-1414_364-1154d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775187 | |||||||
| chr13:51775195 | CCTACATG others(4): Show |
C | 1 | a0002c0002t0006g0063 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.364-1172_364-1162d others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775195 | |||||||
| chr13:51775195 | CCTACATG others(54): Show |
C | 43 | a0001c0001t0001g0039 a0001c0001t0001g0115 a0001c0001t0001g0138 others(40): Show |
50 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.364-1222_364-1162d others(63): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775195 | |||||||
| chr13:51775201 | TGTATTCT others(3): Show |
T | 2 | a0001c0001t0001g0257 a0001c0001t0002g0162 |
2 | HG03654.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.364-1177_364-1168d others(12): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775201 | |||||||
| chr13:51775206 | T | TCTCCTAC others(9): Show |
1 | a0003c0003t0001g0221 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.364-1173_364-1172i others(18): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775206 | |||||||
| chr13:51775225 | TGTATTCT others(102): Show |
T | 25 | a0002c0002t0001g0193 a0002c0002t0003g0002 a0002c0002t0003g0017 others(22): Show |
32 | HG01106.hp1 HG01243.hp1 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.364-1300_364-1192d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775225 | |||||||
| chr13:51775230 | T | TCTC | 3 | a0001c0001t0001g0105 a0001c0001t0001g0123 a0001c0001t0002g0298 |
3 | HG00408.hp2 NA18972.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.364-1197_364-1196i others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775230 | |||||||
| chr13:51775231 | C | G | 2 | a0001c0001t0001g0257 a0001c0001t0002g0162 |
2 | HG03654.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.364-1197G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775231 | |||||||
| chr13:51775231 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.364-1197G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775231 | |||||||
| chr13:51775243 | C | CCTACATG others(4): Show |
6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-1210_364-1209i others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775243 | |||||||
| chr13:51775243 | CCTACAGT others(194): Show |
C | 1 | a0001c0001t0002g0298 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.364-1410_364-1210d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775243 | |||||||
| chr13:51775244 | CTACAGTA others(25): Show |
C | 1 | a0001c0001t0007g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.364-1242_364-1211d others(34): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775244 | |||||||
| chr13:51775248 | A | AT | 6 | a0001c0001t0001g0127 a0001c0001t0001g0234 a0001c0001t0001g0321 others(3): Show |
6 | HG02055.hp1 HG02559.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-1215_364-1214i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775248 | |||||||
| chr13:51775248 | AGTATTCT others(78): Show |
A | 9 | a0001c0001t0003g0259 a0002c0002t0003g0049 a0002c0002t0003g0050 others(6): Show |
10 | HG00735.hp1 HG01109.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.364-1299_364-1215d others(87): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775248 | |||||||
| chr13:51775248 | AGTATTCT others(193): Show |
A | 5 | a0002c0002t0003g0050 a0002c0002t0003g0176 a0002c0002t0003g0249 others(2): Show |
5 | HG01081.hp2 HG01106.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-1414_364-1215d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775248 | |||||||
| chr13:51775254 | CTACTACA others(181): Show |
C | 1 | a0001c0001t0002g0162 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.364-1408_364-1221d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775254 | |||||||
| chr13:51775256 | A | C | 53 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0030 others(50): Show |
65 | HG00438.hp1 HG01515.hp2 HG01975.hp2 others(62): Show |
intron_variant | MODIFIER | c.364-1222T>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775256 | |||||||
| chr13:51775257 | CTACA | C | 4 | a0001c0001t0001g0127 a0001c0001t0001g0234 a0001c0001t0001g0321 others(1): Show |
4 | HG02559.hp2 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-1227_364-1224d others(6): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775257 | |||||||
| chr13:51775261 | AT | A | 3 | a0001c0001t0001g0257 a0002c0002t0003g0017 a0002c0002t0003g0217 |
3 | HG02055.hp1 HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.364-1228delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775261 | |||||||
| chr13:51775262 | T | A | 4 | a0001c0001t0001g0127 a0001c0001t0001g0234 a0001c0001t0001g0321 others(1): Show |
4 | HG02559.hp2 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-1228A>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775262 | |||||||
| chr13:51775267 | TCTCCTAC others(343): Show |
T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0123 |
2 | NA18972.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.363+1443_364-1234d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775267 | |||||||
| chr13:51775271 | CTACAG | C | 3 | a0002c0002t0003g0017 a0002c0002t0003g0217 a0002c0002t0006g0063 |
3 | HG02055.hp1 HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.364-1242_364-1238d others(7): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775271 | |||||||
| chr13:51775275 | AGTACAT | A | 3 | a0001c0001t0001g0127 a0001c0001t0001g0257 a0001c0001t0001g0321 |
3 | HG02559.hp2 HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.364-1247_364-1242d others(8): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775275 | |||||||
| chr13:51775276 | G | C | 1 | a0001c0001t0001g0234 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.364-1242C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775276 | |||||||
| chr13:51775276 | G | GTATTCTC others(1): Show |
5 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-1243_364-1242i others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775276 | |||||||
| chr13:51775281 | TGTATTCT others(6): Show |
T | 1 | a0001c0001t0001g0224 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.364-1260_364-1248d others(15): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775281 | |||||||
| chr13:51775286 | TCTC | T | 3 | a0002c0002t0003g0017 a0002c0002t0003g0217 a0002c0002t0006g0063 |
3 | HG02055.hp1 HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.364-1255_364-1253d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775286 | |||||||
| chr13:51775294 | AGTATTCT others(20): Show |
A | 4 | a0001c0001t0002g0020 a0001c0001t0002g0285 a0001c0001t0002g0305 others(1): Show |
4 | HG02015.hp2 HG02074.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-1287_364-1261d others(29): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775294 | |||||||
| chr13:51775302 | C | CCTACATG others(4): Show |
1 | a0001c0001t0001g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.364-1269_364-1268i others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775302 | |||||||
| chr13:51775302 | CCTACAGT others(135): Show |
C | 6 | a0001c0001t0001g0115 a0001c0001t0002g0061 a0001c0001t0002g0266 others(3): Show |
7 | HG01433.hp2 HG03491.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-1410_364-1269d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775302 | |||||||
| chr13:51775307 | A | AT | 11 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0130 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.364-1274_364-1273i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775307 | |||||||
| chr13:51775307 | AGTATTCT others(7): Show |
A | 1 | a0001c0001t0002g0261 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.364-1287_364-1274d others(16): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775307 | |||||||
| chr13:51775307 | AGTATTCT others(20): Show |
A | 1 | a0001c0001t0001g0304 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.364-1300_364-1274d others(29): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775307 | |||||||
| chr13:51775315 | CCTACATG others(122): Show |
C | 1 | a0001c0001t0002g0306 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.364-1410_364-1282d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775315 | |||||||
| chr13:51775320 | AT | A | 47 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0001t0001g0127 others(44): Show |
52 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.364-1287delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775320 | |||||||
| chr13:51775321 | TGTATTCT others(6): Show |
T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0139 a0001c0001t0001g0152 others(1): Show |
5 | NA18945.hp1 NA18988.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-1300_364-1288d others(15): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775321 | |||||||
| chr13:51775326 | TCTCCTAC others(9): Show |
T | 2 | a0001c0001t0001g0257 a0001c0001t0002g0287 |
2 | HG01516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.364-1308_364-1293d others(18): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775326 | |||||||
| chr13:51775329 | C | CCTACATG others(237): Show |
1 | a0001c0001t0001g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.364-1296_364-1295i others(246): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775329 | |||||||
| chr13:51775334 | A | AT | 37 | a0001c0001t0001g0039 a0001c0001t0001g0138 a0001c0001t0002g0020 others(34): Show |
42 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.364-1301_364-1300i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775334 | |||||||
| chr13:51775334 | A | ATGTATTC others(138): Show |
6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-1301_364-1300i others(147): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775334 | |||||||
| chr13:51775334 | A | T | 9 | a0001c0001t0003g0259 a0002c0002t0003g0049 a0002c0002t0003g0050 others(6): Show |
10 | HG00735.hp1 HG01109.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.364-1300T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775334 | |||||||
| chr13:51775339 | TCTC | T | 35 | a0001c0001t0001g0039 a0001c0001t0001g0138 a0001c0001t0002g0020 others(32): Show |
40 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.364-1308_364-1306d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775339 | |||||||
| chr13:51775342 | C | CCTACATG others(4): Show |
2 | a0001c0001t0001g0234 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.364-1309_364-1308i others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775342 | |||||||
| chr13:51775342 | CCTACAGT others(132): Show |
C | 1 | a0001c0001t0001g0128 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.364-1447_364-1309d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775342 | |||||||
| chr13:51775385 | T | G | 1 | a0002c0002t0003g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.364-1351A>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775385 | |||||||
| chr13:51775385 | T | TGTATTCT others(3): Show |
2 | a0001c0001t0001g0127 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.364-1352_364-1351i others(12): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775385 | |||||||
| chr13:51775385 | TGTATTCT others(57): Show |
T | 2 | a0002c0002t0003g0017 a0002c0002t0003g0217 |
2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.364-1415_364-1352d others(66): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775385 | |||||||
| chr13:51775389 | T | C | 1 | a0001c0001t0001g0257 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.364-1355A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775389 | |||||||
| chr13:51775390 | TCTC | T | 7 | a0001c0001t0001g0234 a0001c0001t0007g0156 a0002c0002t0003g0002 others(4): Show |
8 | HG01884.hp2 HG01891.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.364-1359_364-1357d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775390 | |||||||
| chr13:51775390 | TCTCCTAC others(23): Show |
T | 28 | a0001c0001t0001g0138 a0001c0001t0002g0020 a0001c0001t0002g0285 others(25): Show |
33 | HG00735.hp1 HG01106.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.364-1386_364-1357d others(32): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775390 | |||||||
| chr13:51775390 | TCTCCTAC others(121): Show |
T | 2 | a0001c0001t0002g0056 a0001c0001t0002g0318 |
2 | HG00741.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.364-1484_364-1357d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775390 | |||||||
| chr13:51775390 | TCTCCTAC others(180): Show |
T | 2 | a0001c0001t0002g0273 a0001c0001t0002g0308 |
2 | HG00323.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.363+1483_364-1357d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775390 | |||||||
| chr13:51775390 | TCTCCTAC others(220): Show |
T | 30 | a0001c0001t0001g0039 a0001c0001t0001g0304 a0001c0001t0002g0020 others(27): Show |
34 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.363+1443_364-1357d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775390 | |||||||
| chr13:51775390 | TCTCCTAC others(298): Show |
T | 1 | a0001c0001t0001g0257 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.363+1365_364-1357d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775390 | |||||||
| chr13:51775398 | AT | A | 22 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(19): Show |
24 | HG01884.hp2 HG01891.hp1 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.364-1365delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775398 | |||||||
| chr13:51775399 | TGTATTCT others(6): Show |
T | 1 | a0002c0002t0001g0191 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.364-1378_364-1366d others(15): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775399 | |||||||
| chr13:51775404 | TCTCCTAC others(206): Show |
T | 1 | a0001c0001t0003g0296 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.363+1443_364-1371d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775404 | |||||||
| chr13:51775412 | A | AT | 21 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(18): Show |
23 | HG01884.hp2 HG01891.hp1 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.364-1379_364-1378i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775412 | |||||||
| chr13:51775417 | TCTC | T | 3 | a0001c0001t0007g0156 a0002c0002t0006g0063 a0004c0008t0002g0270 |
3 | HG01884.hp2 HG01981.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.364-1386_364-1384d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775417 | |||||||
| chr13:51775420 | C | CCTACATG others(4): Show |
2 | a0001c0001t0001g0127 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.364-1387_364-1386i others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775420 | |||||||
| chr13:51775420 | CCTACAGT others(54): Show |
C | 7 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0102 others(4): Show |
7 | HG01515.hp2 HG01975.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-1447_364-1387d others(63): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775420 | |||||||
| chr13:51775439 | TGTATTCT others(3): Show |
T | 23 | a0001c0001t0003g0259 a0002c0002t0001g0193 a0002c0002t0003g0002 others(20): Show |
28 | HG00735.hp1 HG01106.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.364-1415_364-1406d others(12): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775439 | |||||||
| chr13:51775444 | T | C | 1 | a0001c0001t0002g0162 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.364-1410A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775444 | |||||||
| chr13:51775444 | T | TCTCCTAC others(60): Show |
6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-1411_364-1410i others(69): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775444 | |||||||
| chr13:51775444 | TCTACAGT others(6): Show |
T | 11 | a0001c0001t0001g0138 a0001c0001t0001g0234 a0001c0001t0002g0020 others(8): Show |
12 | HG01884.hp2 HG01891.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.364-1423_364-1411d others(15): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775444 | |||||||
| chr13:51775449 | A | AT | 6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-1416_364-1415i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775449 | |||||||
| chr13:51775449 | A | T | 6 | a0002c0002t0003g0050 a0002c0002t0003g0176 a0002c0002t0003g0232 others(3): Show |
6 | HG01081.hp2 HG01106.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-1415T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775449 | |||||||
| chr13:51775457 | C | CCTACATG others(4): Show |
2 | a0001c0001t0001g0127 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.364-1424_364-1423i others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775457 | |||||||
| chr13:51775457 | CCTACAGT others(17): Show |
C | 1 | a0003c0003t0001g0237 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.364-1447_364-1424d others(26): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775457 | |||||||
| chr13:51775462 | A | AT | 5 | a0002c0002t0003g0017 a0002c0002t0003g0190 a0002c0002t0003g0218 others(2): Show |
6 | HG02486.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-1429_364-1428i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775462 | |||||||
| chr13:51775462 | AGTATTCT others(139): Show |
A | 3 | a0002c0002t0003g0154 a0002c0002t0003g0175 a0002c0002t0003g0207 |
3 | HG02572.hp1 HG02615.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.363+1452_364-1429d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775462 | |||||||
| chr13:51775462 | AGTATTCT others(254): Show |
A | 2 | a0002c0002t0003g0192 a0002c0002t0003g0209 |
2 | HG02258.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.363+1337_364-1429d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775462 | |||||||
| chr13:51775470 | CCTACATG others(4): Show |
C | 5 | a0002c0002t0003g0017 a0002c0002t0003g0190 a0002c0002t0003g0218 others(2): Show |
6 | HG02486.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-1447_364-1437d others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775470 | |||||||
| chr13:51775480 | T | C | 1 | a0004c0008t0002g0270 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.364-1446A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775480 | |||||||
| chr13:51775481 | TCTACAGT others(30): Show |
T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0161 a0001c0001t0001g0177 others(1): Show |
5 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-1484_364-1448d others(39): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775481 | |||||||
| chr13:51775500 | TGTATTCT others(3): Show |
T | 4 | a0001c0001t0003g0259 a0002c0002t0003g0049 a0002c0002t0003g0050 others(1): Show |
4 | HG00735.hp1 HG01109.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-1476_364-1467d others(12): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775500 | |||||||
| chr13:51775500 | TGTATTCT others(62): Show |
T | 1 | a0002c0002t0003g0049 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.363+1491_364-1467d others(71): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775500 | |||||||
| chr13:51775500 | TGTATTCT others(102): Show |
T | 3 | a0002c0002t0003g0002 a0002c0002t0003g0073 a0002c0002t0003g0080 |
4 | HG01891.hp1 HG01952.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1451_364-1467d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775500 | |||||||
| chr13:51775505 | TCTACAGT others(6): Show |
T | 2 | a0001c0001t0001g0115 a0002c0002t0006g0063 |
2 | HG02572.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.364-1484_364-1472d others(15): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775505 | |||||||
| chr13:51775505 | TCTACAGT others(105): Show |
T | 2 | a0002c0002t0003g0017 a0002c0002t0003g0217 |
2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.363+1443_364-1472d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775505 | |||||||
| chr13:51775508 | A | C | 1 | a0001c0001t0007g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.364-1474T>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775508 | |||||||
| chr13:51775518 | C | CCTACATG others(31): Show |
3 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG02630.hp1 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.364-1485_364-1484i others(40): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775518 | |||||||
| chr13:51775518 | CCTACAGT others(194): Show |
C | 1 | a0001c0001t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.363+1341_364-1485d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775518 | |||||||
| chr13:51775519 | CTACAGTA others(25): Show |
C | 2 | a0001c0001t0002g0306 a0002c0002t0003g0189 |
2 | HG02630.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.363+1509_364-1486d others(34): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775519 | |||||||
| chr13:51775523 | A | AT | 43 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0133 others(40): Show |
49 | HG00408.hp2 HG01081.hp2 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.364-1490_364-1489i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775523 | |||||||
| chr13:51775523 | AGTATTCT others(78): Show |
A | 2 | a0002c0002t0003g0176 a0002c0002t0003g0232 |
2 | HG01361.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.363+1452_364-1490d others(87): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775523 | |||||||
| chr13:51775526 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.364-1492T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775526 | |||||||
| chr13:51775527 | T | C | 4 | a0001c0001t0002g0020 a0001c0001t0002g0285 a0001c0001t0002g0305 others(1): Show |
4 | HG02015.hp2 HG02074.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-1493A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775527 | |||||||
| chr13:51775528 | T | A | 1 | a0001c0001t0001g0234 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.364-1494A>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775528 | |||||||
| chr13:51775528 | TCTC | T | 7 | a0001c0001t0001g0127 a0001c0001t0001g0321 a0001c0001t0002g0061 others(4): Show |
8 | HG01433.hp2 HG02559.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-1497_364-1495d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775528 | |||||||
| chr13:51775528 | TCTCCTAC others(82): Show |
T | 6 | a0001c0001t0002g0162 a0001c0001t0002g0298 a0002c0002t0003g0017 others(3): Show |
7 | HG00408.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.363+1443_364-1495d others(91): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775528 | |||||||
| chr13:51775528 | TCTCCTAC others(160): Show |
T | 4 | a0001c0001t0002g0020 a0001c0001t0002g0285 a0001c0001t0002g0305 others(1): Show |
4 | HG02015.hp2 HG02074.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1365_364-1495d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775528 | |||||||
| chr13:51775536 | AT | A | 34 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0133 others(31): Show |
39 | HG01081.hp2 HG01106.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.364-1503delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775536 | |||||||
| chr13:51775542 | TCTCCTAC others(68): Show |
T | 3 | a0001c0001t0002g0056 a0001c0001t0002g0318 a0004c0008t0002g0270 |
3 | HG00741.hp2 HG01515.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.363+1443_364-1509d others(77): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775542 | |||||||
| chr13:51775543 | CTCCTACA others(1): Show |
C | 3 | a0001c0001t0001g0084 a0001c0001t0001g0115 a0002c0002t0006g0063 |
3 | HG02572.hp2 NA18982.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.363+1509_364-1510d others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775543 | |||||||
| chr13:51775546 | CTACAG | C | 30 | a0001c0001t0001g0234 a0001c0001t0001g0321 a0001c0001t0002g0061 others(27): Show |
35 | HG01081.hp2 HG01106.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.363+1509_363+1513d others(7): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775546 | |||||||
| chr13:51775550 | A | ATGTATT | 4 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0133 others(1): Show |
4 | HG02818.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+1509_363+1510i others(8): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775550 | |||||||
| chr13:51775550 | AGTACAT | A | 4 | a0001c0001t0003g0259 a0002c0002t0003g0049 a0002c0002t0003g0050 others(1): Show |
4 | HG00735.hp1 HG01109.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1504_363+1509d others(8): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775550 | |||||||
| chr13:51775551 | G | C | 4 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0133 others(1): Show |
4 | HG02818.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+1509C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775551 | |||||||
| chr13:51775551 | G | GTATTCTC others(1): Show |
3 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG02630.hp1 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.363+1508_363+1509i others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775551 | |||||||
| chr13:51775555 | AT | A | 7 | a0001c0001t0001g0084 a0001c0001t0001g0115 a0001c0001t0001g0127 others(4): Show |
7 | HG02572.hp2 HG02818.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.363+1504delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775555 | |||||||
| chr13:51775561 | TCTC | T | 24 | a0001c0001t0001g0234 a0001c0001t0001g0321 a0002c0002t0001g0193 others(21): Show |
28 | HG01081.hp2 HG01106.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.363+1496_363+1498d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775561 | |||||||
| chr13:51775561 | TCTCCTAC others(49): Show |
T | 6 | a0001c0001t0002g0061 a0001c0001t0002g0266 a0001c0001t0002g0267 others(3): Show |
7 | HG01433.hp2 HG03491.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.363+1443_363+1498d others(58): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775561 | |||||||
| chr13:51775569 | A | AT | 10 | a0001c0001t0001g0084 a0001c0001t0001g0127 a0001c0001t0001g0130 others(7): Show |
10 | HG00735.hp1 HG01109.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+1490_363+1491i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775569 | |||||||
| chr13:51775572 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.363+1488T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775572 | |||||||
| chr13:51775574 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.363+1486A>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775574 | |||||||
| chr13:51775574 | TCTC | T | 7 | a0001c0001t0001g0084 a0001c0001t0001g0127 a0001c0001t0003g0259 others(4): Show |
7 | HG00735.hp1 HG01109.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.363+1483_363+1485d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775574 | |||||||
| chr13:51775577 | C | CCTACATG others(4): Show |
3 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG02630.hp1 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.363+1482_363+1483i others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775577 | |||||||
| chr13:51775582 | A | AT | 26 | a0001c0001t0001g0234 a0001c0001t0001g0321 a0001c0001t0007g0156 others(23): Show |
30 | HG01081.hp2 HG01106.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.363+1477_363+1478i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775582 | |||||||
| chr13:51775587 | TCTC | T | 4 | a0001c0001t0001g0234 a0001c0001t0001g0321 a0001c0001t0007g0156 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1470_363+1472d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775587 | |||||||
| chr13:51775595 | AT | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(116): Show |
157 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(154): Show |
intron_variant | MODIFIER | c.363+1464delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775595 | |||||||
| chr13:51775596 | TGTATTCT others(6): Show |
T | 22 | a0001c0001t0001g0258 a0001c0001t0001g0264 a0001c0001t0001g0271 others(19): Show |
26 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.363+1451_363+1463d others(15): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775596 | |||||||
| chr13:51775601 | TCTC | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0115 a0001c0001t0001g0127 |
3 | HG03516.hp1 NA18982.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.363+1456_363+1458d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775601 | |||||||
| chr13:51775601 | TCTCCTAC others(9): Show |
T | 3 | a0001c0001t0001g0128 a0001c0001t0002g0273 a0001c0001t0002g0308 |
3 | HG00323.hp1 HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.363+1443_363+1458d others(18): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775601 | |||||||
| chr13:51775601 | TCTCCTAC others(124): Show |
T | 1 | a0001c0001t0004g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.363+1328_363+1458d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775601 | |||||||
| chr13:51775609 | A | AGTATTCT others(7): Show |
3 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG02630.hp1 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.363+1450_363+1451i others(16): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775609 | |||||||
| chr13:51775609 | A | AGTATTCT others(133): Show |
1 | a0001c0001t0001g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.363+1450_363+1451i others(142): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775609 | |||||||
| chr13:51775609 | A | AT | 115 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(112): Show |
153 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(150): Show |
intron_variant | MODIFIER | c.363+1450_363+1451i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775609 | |||||||
| chr13:51775609 | A | ATGTATTC others(114): Show |
2 | a0001c0001t0001g0152 a0001c0001t0001g0164 |
2 | NA18945.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.363+1450_363+1451i others(123): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775609 | |||||||
| chr13:51775609 | A | T | 5 | a0002c0002t0003g0154 a0002c0002t0003g0175 a0002c0002t0003g0176 others(2): Show |
5 | HG01361.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+1451T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775609 | |||||||
| chr13:51775614 | TCTC | T | 90 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(87): Show |
124 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(121): Show |
intron_variant | MODIFIER | c.363+1443_363+1445d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775614 | |||||||
| chr13:51775614 | TCTCCTAC others(244): Show |
T | 1 | a0001c0001t0001g0075 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.363+1195_363+1445d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775614 | |||||||
| chr13:51775617 | C | CCTACATG others(4): Show |
2 | a0001c0001t0001g0127 a0001c0001t0001g0213 |
2 | HG02602.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.363+1442_363+1443i others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775617 | |||||||
| chr13:51775617 | C | CCTACATG others(82): Show |
2 | a0001c0001t0001g0130 a0001c0001t0001g0133 |
2 | HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.363+1442_363+1443i others(91): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775617 | |||||||
| chr13:51775617 | CCTACAGT others(474): Show |
C | 1 | a0001c0001t0001g0250 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.363+962_363+1442de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775617 | |||||||
| chr13:51775622 | A | AT | 5 | a0001c0001t0001g0084 a0001c0001t0003g0259 a0002c0002t0003g0049 others(2): Show |
5 | HG00735.hp1 HG01109.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+1437_363+1438i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775622 | |||||||
| chr13:51775626 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.363+1434A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775626 | |||||||
| chr13:51775627 | TCTCCTAC others(61): Show |
T | 1 | a0001c0001t0001g0084 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.363+1365_363+1432d others(70): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775627 | |||||||
| chr13:51775627 | TCTCCTAC others(98): Show |
T | 4 | a0001c0001t0003g0259 a0002c0002t0003g0049 a0002c0002t0003g0050 others(1): Show |
4 | HG00735.hp1 HG01109.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1328_363+1432d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775627 | |||||||
| chr13:51775640 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0304 |
3 | HG00423.hp1 NA18991.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.363+1420A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775640 | |||||||
| chr13:51775660 | T | TGTACTCT others(3): Show |
21 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0030 others(18): Show |
31 | HG02040.hp2 HG02486.hp1 HG02602.hp1 others(28): Show |
intron_variant | MODIFIER | c.363+1399_363+1400i others(12): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775660 | |||||||
| chr13:51775660 | T | TGTATTCT others(3): Show |
3 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG02630.hp1 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.363+1399_363+1400i others(12): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775660 | |||||||
| chr13:51775660 | TGTATTCT others(20): Show |
T | 1 | a0002c0002t0006g0063 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.363+1373_363+1399d others(29): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775660 | |||||||
| chr13:51775660 | TGTATTCT others(57): Show |
T | 20 | a0002c0002t0001g0193 a0002c0002t0003g0002 a0002c0002t0003g0042 others(17): Show |
24 | HG01081.hp2 HG01106.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.363+1336_363+1399d others(66): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775660 | |||||||
| chr13:51775664 | T | C | 12 | a0001c0001t0001g0030 a0001c0001t0001g0139 a0001c0001t0001g0188 others(9): Show |
13 | HG00323.hp1 HG00741.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.363+1396A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775664 | |||||||
| chr13:51775665 | TCTC | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(102): Show |
129 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.363+1392_363+1394d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775665 | |||||||
| chr13:51775665 | TCTCCTAC others(10): Show |
T | 1 | a0001c0001t0001g0304 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.363+1378_363+1394d others(19): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775665 | |||||||
| chr13:51775665 | TCTCCTAC others(23): Show |
T | 12 | a0001c0001t0001g0030 a0001c0001t0001g0139 a0001c0001t0001g0188 others(9): Show |
13 | HG00323.hp1 HG00741.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.363+1365_363+1394d others(32): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775665 | |||||||
| chr13:51775665 | TCTCCTAC others(60): Show |
T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
5 | HG00423.hp1 HG02145.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+1328_363+1394d others(69): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775665 | |||||||
| chr13:51775665 | TCTCCTAC others(167): Show |
T | 1 | a0001c0001t0004g0007 | 3 | HG02109.hp1 HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.363+1221_363+1394d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775665 | |||||||
| chr13:51775665 | TCTCCTAC others(193): Show |
T | 1 | a0001c0001t0001g0128 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.363+1195_363+1394d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775665 | |||||||
| chr13:51775673 | AT | A | 125 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(122): Show |
153 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.363+1386delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775673 | |||||||
| chr13:51775674 | TGTATTCT others(6): Show |
T | 2 | a0003c0003t0001g0237 a0003c0003t0001g0238 |
2 | HG01934.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.363+1373_363+1385d others(15): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775674 | |||||||
| chr13:51775679 | TCTC | T | 22 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0030 others(19): Show |
32 | HG02040.hp2 HG02486.hp1 HG02602.hp1 others(29): Show |
intron_variant | MODIFIER | c.363+1378_363+1380d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775679 | |||||||
| chr13:51775682 | CCTACAGT others(67): Show |
C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0161 a0001c0001t0001g0177 others(1): Show |
5 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+1304_363+1377d others(76): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775682 | |||||||
| chr13:51775687 | A | AT | 24 | a0001c0001t0001g0115 a0001c0001t0001g0127 a0001c0001t0001g0134 others(21): Show |
27 | HG01106.hp2 HG01361.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.363+1372_363+1373i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775687 | |||||||
| chr13:51775687 | A | ATGTATTC others(96): Show |
2 | a0001c0001t0001g0130 a0001c0001t0001g0133 |
2 | HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.363+1372_363+1373i others(105): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775687 | |||||||
| chr13:51775687 | AG | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(92): Show |
119 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.363+1372delC | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775687 | |||||||
| chr13:51775690 | A | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(92): Show |
119 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.363+1370T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775690 | |||||||
| chr13:51775692 | T | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(92): Show |
119 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.363+1368A>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775692 | |||||||
| chr13:51775692 | TCTC | T | 14 | a0001c0001t0001g0115 a0001c0001t0001g0127 a0001c0001t0001g0321 others(11): Show |
16 | HG01884.hp2 HG01981.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.363+1365_363+1367d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775692 | |||||||
| chr13:51775692 | TCTCCTAC others(33): Show |
T | 3 | a0002c0002t0003g0072 a0002c0002t0003g0244 a0002c0002t0003g0249 |
3 | HG01106.hp2 HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.363+1328_363+1367d others(42): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775692 | |||||||
| chr13:51775694 | TC | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(92): Show |
119 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.363+1365delG | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775694 | |||||||
| chr13:51775695 | C | CCTACATG others(4): Show |
3 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG02630.hp1 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.363+1364_363+1365i others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775695 | |||||||
| chr13:51775714 | TGTATTCT others(3): Show |
T | 4 | a0001c0001t0007g0156 a0002c0002t0003g0154 a0002c0002t0003g0175 others(1): Show |
4 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+1336_363+1345d others(12): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775714 | |||||||
| chr13:51775719 | T | TCTCCTAC others(87): Show |
3 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG02630.hp1 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.363+1340_363+1341i others(96): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775719 | |||||||
| chr13:51775719 | TCTACAGT others(6): Show |
T | 11 | a0001c0001t0001g0115 a0001c0001t0001g0127 a0001c0001t0002g0261 others(8): Show |
13 | HG01981.hp1 HG02055.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.363+1328_363+1340d others(15): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775719 | |||||||
| chr13:51775724 | A | AT | 3 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG02630.hp1 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.363+1335_363+1336i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775724 | |||||||
| chr13:51775724 | A | T | 2 | a0002c0002t0003g0192 a0002c0002t0003g0209 |
2 | HG02258.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.363+1336T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775724 | |||||||
| chr13:51775732 | C | CCTACATG others(4): Show |
4 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0234 others(1): Show |
4 | HG02559.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+1327_363+1328i others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775732 | |||||||
| chr13:51775732 | C | CCTACATG others(58): Show |
1 | a0001c0001t0001g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.363+1327_363+1328i others(67): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775732 | |||||||
| chr13:51775732 | CCTACAGT others(17): Show |
C | 1 | a0001c0001t0001g0206 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.363+1304_363+1327d others(26): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775732 | |||||||
| chr13:51775737 | A | AT | 26 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0030 others(23): Show |
37 | HG01891.hp1 HG01952.hp1 HG02004.hp2 others(34): Show |
intron_variant | MODIFIER | c.363+1322_363+1323i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775737 | |||||||
| chr13:51775737 | AGTATTCT others(112): Show |
A | 1 | a0002c0002t0003g0232 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.363+1204_363+1322d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775737 | |||||||
| chr13:51775745 | CCTACATG others(4): Show |
C | 4 | a0002c0002t0003g0002 a0002c0002t0003g0073 a0002c0002t0003g0080 others(1): Show |
5 | HG01891.hp1 HG01952.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+1304_363+1314d others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775745 | |||||||
| chr13:51775755 | T | C | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | HG01981.hp1 HG02145.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+1305A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775755 | |||||||
| chr13:51775756 | TCTACAGT others(211): Show |
T | 1 | a0001c0001t0001g0304 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.363+1086_363+1303d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775756 | |||||||
| chr13:51775770 | CTACATGT others(49): Show |
C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0139 a0001c0001t0007g0156 |
3 | HG01884.hp2 NA18988.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.363+1234_363+1289d others(58): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775770 | |||||||
| chr13:51775775 | TGTATTCT others(88): Show |
T | 1 | a0001c0001t0001g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.363+1190_363+1284d others(97): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775775 | |||||||
| chr13:51775775 | TGTATTCT others(112): Show |
T | 1 | a0001c0001t0001g0030 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.363+1166_363+1284d others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775775 | |||||||
| chr13:51775779 | T | C | 1 | a0001c0001t0003g0296 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.363+1281A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775779 | |||||||
| chr13:51775780 | T | TCTC | 3 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG02818.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.363+1279_363+1280i others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775780 | |||||||
| chr13:51775780 | TCTACAGT others(65): Show |
T | 1 | a0001c0001t0001g0135 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.363+1208_363+1279d others(74): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775780 | |||||||
| chr13:51775780 | TCTACAGT others(78): Show |
T | 9 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0070 others(6): Show |
12 | HG00423.hp1 HG01243.hp1 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.363+1195_363+1279d others(87): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775780 | |||||||
| chr13:51775793 | C | CCTACATG others(4): Show |
3 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG02818.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.363+1266_363+1267i others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775793 | |||||||
| chr13:51775793 | C | CCTACATG others(31): Show |
3 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG02630.hp1 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.363+1266_363+1267i others(40): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775793 | |||||||
| chr13:51775794 | CTACAGTA others(25): Show |
C | 7 | a0001c0001t0001g0138 a0002c0002t0003g0042 a0002c0002t0003g0050 others(4): Show |
7 | HG01109.hp1 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.363+1234_363+1265d others(34): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775794 | |||||||
| chr13:51775798 | A | AT | 154 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(151): Show |
196 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.363+1261_363+1262i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775798 | |||||||
| chr13:51775798 | AGTATTCT others(51): Show |
A | 6 | a0001c0001t0003g0259 a0001c0001t0003g0296 a0002c0002t0003g0049 others(3): Show |
6 | HG00735.hp1 HG02148.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.363+1204_363+1261d others(60): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775798 | |||||||
| chr13:51775803 | TCTC | T | 27 | a0001c0001t0001g0234 a0001c0001t0001g0321 a0002c0002t0001g0193 others(24): Show |
34 | HG01081.hp2 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.363+1254_363+1256d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775803 | |||||||
| chr13:51775803 | TCTCCTAC others(55): Show |
T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(101): Show |
129 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.363+1195_363+1256d others(64): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775803 | |||||||
| chr13:51775811 | AT | A | 30 | a0001c0001t0001g0234 a0001c0001t0001g0321 a0002c0002t0001g0193 others(27): Show |
37 | HG01081.hp2 HG01106.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.363+1248delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775811 | |||||||
| chr13:51775817 | TCTCCTAC others(15): Show |
T | 1 | a0001c0001t0002g0261 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.363+1221_363+1242d others(24): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775817 | |||||||
| chr13:51775817 | TCTCCTAC others(28): Show |
T | 1 | a0004c0008t0002g0270 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.363+1208_363+1242d others(37): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775817 | |||||||
| chr13:51775817 | TCTCCTAC others(41): Show |
T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.363+1195_363+1242d others(50): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775817 | |||||||
| chr13:51775818 | CTCCTACA others(1): Show |
C | 20 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0038 others(17): Show |
30 | HG02040.hp2 HG02486.hp1 HG02602.hp1 others(27): Show |
intron_variant | MODIFIER | c.363+1234_363+1241d others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775818 | |||||||
| chr13:51775821 | CTACAG | C | 28 | a0002c0002t0001g0193 a0002c0002t0003g0002 a0002c0002t0003g0017 others(25): Show |
35 | HG01081.hp2 HG01106.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.363+1234_363+1238d others(7): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775821 | |||||||
| chr13:51775826 | G | C | 1 | a0001c0001t0001g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.363+1234C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775826 | |||||||
| chr13:51775826 | G | GTATTCTC others(1): Show |
7 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0130 others(4): Show |
7 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.363+1233_363+1234i others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775826 | |||||||
| chr13:51775830 | AT | A | 21 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0038 others(18): Show |
31 | HG02040.hp2 HG02486.hp1 HG02559.hp2 others(28): Show |
intron_variant | MODIFIER | c.363+1229delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775830 | |||||||
| chr13:51775831 | TGTATTCT others(6): Show |
T | 6 | a0001c0001t0001g0093 a0001c0001t0001g0110 a0001c0001t0001g0150 others(3): Show |
7 | HG02257.hp2 HG02647.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.363+1216_363+1228d others(15): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775831 | |||||||
| chr13:51775836 | TCTC | T | 11 | a0001c0001t0001g0127 a0001c0001t0001g0138 a0002c0002t0003g0002 others(8): Show |
12 | HG01106.hp2 HG01891.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.363+1221_363+1223d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775836 | |||||||
| chr13:51775844 | A | AT | 20 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0038 others(17): Show |
30 | HG02040.hp2 HG02486.hp1 HG02602.hp1 others(27): Show |
intron_variant | MODIFIER | c.363+1215_363+1216i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775844 | |||||||
| chr13:51775844 | AGTATTCT others(5): Show |
A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0139 |
2 | NA18988.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.363+1204_363+1215d others(14): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775844 | |||||||
| chr13:51775849 | TCTC | T | 14 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0038 others(11): Show |
21 | HG02040.hp2 HG02486.hp1 HG02602.hp1 others(18): Show |
intron_variant | MODIFIER | c.363+1208_363+1210d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775849 | |||||||
| chr13:51775852 | C | CCTACATG others(28): Show |
5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(2): Show |
5 | HG02818.hp1 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+1207_363+1208i others(37): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775852 | |||||||
| chr13:51775857 | A | AGTATTCT others(454): Show |
3 | a0001c0001t0001g0129 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG02818.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.363+1202_363+1203i others(463): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775857 | |||||||
| chr13:51775857 | A | AT | 45 | a0001c0001t0001g0127 a0001c0001t0001g0234 a0001c0001t0001g0321 others(42): Show |
58 | HG01081.hp2 HG01106.hp1 HG01106.hp2 others(55): Show |
intron_variant | MODIFIER | c.363+1202_363+1203i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775857 | |||||||
| chr13:51775857 | A | ATGTATTC others(42): Show |
1 | a0001c0001t0001g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.363+1202_363+1203i others(51): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775857 | |||||||
| chr13:51775857 | A | T | 9 | a0001c0001t0001g0030 a0001c0001t0001g0139 a0001c0001t0003g0259 others(6): Show |
9 | HG00735.hp1 HG01361.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.363+1203T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775857 | |||||||
| chr13:51775862 | TCTC | T | 39 | a0001c0001t0001g0030 a0001c0001t0001g0139 a0001c0001t0001g0234 others(36): Show |
50 | HG01081.hp2 HG01106.hp1 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.363+1195_363+1197d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775862 | |||||||
| chr13:51775865 | C | CCTACATG others(478): Show |
2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.363+1194_363+1195i others(487): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775865 | |||||||
| chr13:51775865 | CCTACAGT others(226): Show |
C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0215 |
2 | HG01123.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.363+962_363+1194de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775865 | |||||||
| chr13:51775870 | A | AT | 16 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0038 others(13): Show |
23 | HG01981.hp1 HG02040.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.363+1189_363+1190i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775870 | |||||||
| chr13:51775878 | CCTACATG others(4): Show |
C | 1 | a0001c0001t0001g0325 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.363+1171_363+1181d others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775878 | |||||||
| chr13:51775884 | TGTATTCT others(3): Show |
T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0139 |
2 | NA18988.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.363+1166_363+1175d others(12): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775884 | |||||||
| chr13:51775888 | T | C | 1 | a0001c0001t0003g0326 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.363+1172A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775888 | |||||||
| chr13:51775889 | TCTACAGT others(78): Show |
T | 1 | a0001c0001t0001g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.363+1086_363+1170d others(87): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775889 | |||||||
| chr13:51775902 | CCTACATG others(4): Show |
C | 2 | a0001c0001t0003g0076 a0001c0001t0004g0064 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.363+1147_363+1157d others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775902 | |||||||
| chr13:51775912 | T | C | 19 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0038 others(16): Show |
29 | HG02040.hp2 HG02486.hp1 HG02602.hp1 others(26): Show |
intron_variant | MODIFIER | c.363+1148A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775912 | |||||||
| chr13:51775912 | TTCTACAG others(17): Show |
T | 1 | a0001c0001t0001g0325 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.363+1124_363+1147d others(26): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775912 | |||||||
| chr13:51775913 | T | TCTC | 13 | a0001c0001t0001g0234 a0001c0001t0001g0321 a0001c0001t0003g0326 others(10): Show |
15 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.363+1146_363+1147i others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775913 | |||||||
| chr13:51775932 | TGTACTCT others(3): Show |
T | 1 | a0004c0008t0002g0270 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.363+1118_363+1127d others(12): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775932 | |||||||
| chr13:51775932 | TGTACTCT others(27): Show |
T | 4 | a0001c0001t0007g0156 a0002c0002t0003g0154 a0002c0002t0003g0175 others(1): Show |
4 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+1094_363+1127d others(36): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775932 | |||||||
| chr13:51775936 | C | T | 80 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0038 others(77): Show |
101 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(98): Show |
intron_variant | MODIFIER | c.363+1124G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775936 | |||||||
| chr13:51775937 | T | TCTC | 19 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0038 others(16): Show |
29 | HG02040.hp2 HG02486.hp1 HG02602.hp1 others(26): Show |
intron_variant | MODIFIER | c.363+1122_363+1123i others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775937 | |||||||
| chr13:51775956 | TGTATTCT others(3): Show |
T | 8 | a0002c0002t0003g0017 a0002c0002t0003g0189 a0002c0002t0003g0190 others(5): Show |
10 | HG01106.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+1094_363+1103d others(12): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775956 | |||||||
| chr13:51775960 | T | C | 4 | a0001c0001t0001g0102 a0001c0001t0001g0121 a0001c0001t0001g0138 others(1): Show |
4 | HG02258.hp2 HG03704.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+1100A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775960 | |||||||
| chr13:51775961 | T | TCTCCTAC others(675): Show |
1 | a0001c0001t0001g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.363+1098_363+1099i others(684): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775961 | |||||||
| chr13:51775961 | TCTACAGT others(6): Show |
T | 20 | a0001c0001t0001g0102 a0001c0001t0001g0121 a0001c0001t0001g0135 others(17): Show |
22 | HG00735.hp1 HG01243.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.363+1086_363+1098d others(15): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775961 | |||||||
| chr13:51775966 | AGTATTCT others(44): Show |
A | 4 | a0001c0001t0001g0138 a0001c0001t0001g0150 a0001c0001t0001g0177 others(1): Show |
4 | HG02257.hp2 HG02258.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1043_363+1093d others(53): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775966 | |||||||
| chr13:51775966 | AGTATTCT others(106): Show |
A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.363+981_363+1093de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775966 | |||||||
| chr13:51775974 | C | CCTACATG others(4): Show |
25 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0038 others(22): Show |
35 | HG02040.hp2 HG02486.hp1 HG02559.hp2 others(32): Show |
intron_variant | MODIFIER | c.363+1085_363+1086i others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775974 | |||||||
| chr13:51775974 | CCTACAGT others(55): Show |
C | 3 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0091 |
3 | HG00408.hp1 HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.363+1024_363+1085d others(64): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775974 | |||||||
| chr13:51775974 | CCTACAGT others(117): Show |
C | 1 | a0001c0001t0002g0318 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.363+962_363+1085de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775974 | |||||||
| chr13:51775979 | A | AT | 20 | a0002c0002t0001g0193 a0002c0002t0003g0002 a0002c0002t0003g0044 others(17): Show |
24 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.363+1080_363+1081i others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775979 | |||||||
| chr13:51775987 | CCTACATG others(42): Show |
C | 1 | a0002c0002t0003g0049 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.363+1024_363+1072d others(51): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775987 | |||||||
| chr13:51775987 | CCTACATG others(104): Show |
C | 8 | a0002c0002t0001g0193 a0002c0002t0003g0044 a0002c0002t0003g0141 others(5): Show |
9 | HG01109.hp2 HG01934.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.363+962_363+1072de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775987 | |||||||
| chr13:51775992 | ATGTATTC others(18): Show |
A | 11 | a0002c0002t0003g0002 a0002c0002t0003g0050 a0002c0002t0003g0072 others(8): Show |
14 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.363+1043_363+1067d others(27): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51775992 | |||||||
| chr13:51776003 | AGTATTCT others(7): Show |
A | 9 | a0001c0001t0001g0149 a0001c0001t0001g0161 a0001c0001t0004g0021 others(6): Show |
9 | HG01106.hp2 HG02145.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.363+1043_363+1056d others(16): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776003 | |||||||
| chr13:51776003 | AGTATTCT others(69): Show |
A | 5 | a0001c0001t0001g0135 a0001c0001t0007g0156 a0002c0002t0003g0042 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+981_363+1056de others(77): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776003 | |||||||
| chr13:51776011 | CCTACATG others(80): Show |
C | 3 | a0001c0001t0001g0102 a0001c0001t0001g0121 a0001c0001t0002g0261 |
3 | HG03704.hp1 HG04204.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.363+962_363+1048de others(88): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776011 | |||||||
| chr13:51776017 | T | TGTATTCT others(3): Show |
21 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0038 others(18): Show |
31 | HG02040.hp2 HG02486.hp1 HG02602.hp1 others(28): Show |
intron_variant | MODIFIER | c.363+1042_363+1043i others(12): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776017 | |||||||
| chr13:51776017 | T | TGTATTCT others(6): Show |
5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(2): Show |
5 | HG02818.hp1 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+1030_363+1042d others(15): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776017 | |||||||
| chr13:51776025 | CCTACATG others(4): Show |
C | 11 | a0001c0001t0001g0321 a0001c0001t0003g0259 a0002c0002t0003g0002 others(8): Show |
14 | HG00735.hp1 HG01361.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.363+1024_363+1034d others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776025 | |||||||
| chr13:51776025 | CCTACATG others(66): Show |
C | 1 | a0004c0008t0002g0270 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.363+962_363+1034de others(74): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776025 | |||||||
| chr13:51776030 | ATGTATTC others(42): Show |
A | 4 | a0001c0001t0003g0296 a0002c0002t0003g0080 a0002c0002t0003g0192 others(1): Show |
4 | HG02004.hp2 HG02258.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+981_363+1029de others(50): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776030 | |||||||
| chr13:51776030 | ATGTATTC others(104): Show |
A | 1 | a0002c0002t0003g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.363+919_363+1029de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776030 | |||||||
| chr13:51776035 | T | C | 2 | a0001c0001t0001g0161 a0001c0001t0004g0021 |
2 | HG02647.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.363+1025A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776035 | |||||||
| chr13:51776035 | TTCTACAG others(116): Show |
T | 1 | a0001c0001t0001g0083 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.363+902_363+1024de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776035 | |||||||
| chr13:51776041 | AGTATTCT others(31): Show |
A | 1 | a0001c0001t0003g0259 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.363+981_363+1018de others(39): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776041 | |||||||
| chr13:51776055 | TGTATTCT others(3): Show |
T | 23 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0038 others(20): Show |
33 | HG01106.hp2 HG02040.hp2 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.363+995_363+1004de others(11): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776055 | |||||||
| chr13:51776059 | T | C | 3 | a0001c0001t0001g0150 a0001c0001t0001g0177 a0001c0001t0004g0021 |
3 | HG02257.hp2 HG02896.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.363+1001A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776059 | |||||||
| chr13:51776059 | TTCTACAG others(117): Show |
T | 100 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(97): Show |
128 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.363+877_363+1000de others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776059 | |||||||
| chr13:51776065 | AGTATTCT others(7): Show |
A | 17 | a0001c0001t0001g0035 a0001c0001t0001g0138 a0001c0001t0001g0146 others(14): Show |
22 | HG01192.hp2 HG01255.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.363+981_363+994del others(14): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776065 | |||||||
| chr13:51776065 | AGTATTCT others(69): Show |
A | 2 | a0002c0002t0003g0049 a0002c0002t0003g0232 |
2 | HG01361.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.363+919_363+994del others(76): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776065 | |||||||
| chr13:51776078 | AT | A | 25 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0038 others(22): Show |
35 | HG01106.hp2 HG02040.hp2 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.363+981delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776078 | |||||||
| chr13:51776079 | T | TGTACTCT others(3): Show |
1 | a0001c0001t0001g0234 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.363+980_363+981ins others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776079 | |||||||
| chr13:51776079 | T | TGTATTCT others(3): Show |
2 | a0001c0001t0001g0127 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.363+980_363+981ins others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776079 | |||||||
| chr13:51776079 | T | TGTATTCT others(153): Show |
1 | a0001c0001t0001g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.363+980_363+981ins others(160): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776079 | |||||||
| chr13:51776079 | T | TGTATTCT others(351): Show |
4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG02818.hp1 HG02965.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+980_363+981ins others(358): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776079 | |||||||
| chr13:51776079 | T | TGTATTCT others(327): Show |
1 | a0001c0001t0001g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.363+980_363+981ins others(334): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776079 | |||||||
| chr13:51776083 | TTCTCCTA others(93): Show |
T | 5 | a0001c0001t0001g0035 a0001c0001t0001g0151 a0001c0001t0001g0160 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+877_363+976del others(100): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776083 | |||||||
| chr13:51776084 | TCTC | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0177 a0001c0001t0004g0021 |
3 | HG02257.hp2 HG02896.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.363+973_363+975del others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776084 | |||||||
| chr13:51776087 | CCTACATG others(4): Show |
C | 1 | a0002c0002t0003g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.363+962_363+972del others(11): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776087 | |||||||
| chr13:51776087 | CCTACATG others(66): Show |
C | 10 | a0002c0002t0003g0002 a0002c0002t0003g0050 a0002c0002t0003g0074 others(7): Show |
12 | HG01106.hp1 HG01109.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.363+900_363+972del others(73): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776087 | |||||||
| chr13:51776092 | AT | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0177 a0001c0001t0004g0021 |
3 | HG02257.hp2 HG02896.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.363+967delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776092 | |||||||
| chr13:51776092 | ATGTATTC others(42): Show |
A | 1 | a0002c0002t0003g0050 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.363+919_363+967del others(49): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776092 | |||||||
| chr13:51776097 | T | C | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG02145.hp1 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.363+963A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776097 | |||||||
| chr13:51776097 | TTCTACAG others(79): Show |
T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG01192.hp2 HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.363+877_363+962del others(86): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776097 | |||||||
| chr13:51776098 | T | TCTC | 3 | a0001c0001t0001g0150 a0001c0001t0001g0177 a0001c0001t0004g0021 |
3 | HG02257.hp2 HG02896.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.363+961_363+962ins others(3): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776098 | |||||||
| chr13:51776117 | TGTATTCT others(3): Show |
T | 10 | a0002c0002t0003g0002 a0002c0002t0003g0017 a0002c0002t0003g0073 others(7): Show |
13 | HG01106.hp2 HG01891.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.363+933_363+942del others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776117 | |||||||
| chr13:51776117 | TGTATTCT others(41): Show |
T | 2 | a0001c0001t0001g0161 a0001c0001t0004g0021 |
2 | HG02647.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.363+895_363+942del others(48): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776117 | |||||||
| chr13:51776121 | TTCTACAG others(55): Show |
T | 4 | a0001c0001t0001g0225 a0001c0001t0004g0007 a0002c0002t0003g0049 others(1): Show |
6 | HG01167.hp2 HG01255.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.363+877_363+938del others(62): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776121 | |||||||
| chr13:51776127 | AGTATTCT others(7): Show |
A | 11 | a0001c0001t0001g0138 a0001c0001t0007g0156 a0002c0002t0001g0193 others(8): Show |
12 | HG01109.hp2 HG01884.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.363+919_363+932del others(14): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776127 | |||||||
| chr13:51776140 | AT | A | 10 | a0002c0002t0003g0002 a0002c0002t0003g0017 a0002c0002t0003g0073 others(7): Show |
13 | HG01106.hp2 HG01891.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.363+919delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776140 | |||||||
| chr13:51776141 | T | TGTATTCT others(3): Show |
7 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(4): Show |
7 | HG02630.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.363+918_363+919ins others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776141 | |||||||
| chr13:51776141 | T | TGTATTCT others(6): Show |
1 | a0001c0001t0001g0179 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.363+906_363+918dup others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776141 | |||||||
| chr13:51776141 | T | TGTATTCT others(17): Show |
1 | a0001c0001t0008g0328 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+895_363+918dup others(24): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776141 | |||||||
| chr13:51776145 | TTCTCCTA others(31): Show |
T | 1 | a0001c0001t0004g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.363+877_363+914del others(38): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776145 | |||||||
| chr13:51776149 | CCTACATG others(4): Show |
C | 29 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0038 others(26): Show |
39 | HG00735.hp1 HG01243.hp1 HG02040.hp2 others(36): Show |
intron_variant | MODIFIER | c.363+900_363+910del others(11): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776149 | |||||||
| chr13:51776159 | TTCTACAG others(17): Show |
T | 16 | a0001c0001t0001g0138 a0001c0001t0001g0150 a0001c0001t0001g0177 others(13): Show |
19 | HG01081.hp2 HG01106.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.363+877_363+900del others(24): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776159 | |||||||
| chr13:51776173 | CCTACATG others(4): Show |
C | 1 | a0002c0002t0003g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.363+876_363+886del others(11): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776173 | |||||||
| chr13:51776179 | TGTACTCT others(3): Show |
T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.363+871_363+880del others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776179 | |||||||
| chr13:51776183 | C | T | 72 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0038 others(69): Show |
85 | HG00639.hp1 HG00735.hp1 HG01106.hp1 others(82): Show |
intron_variant | MODIFIER | c.363+877G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776183 | |||||||
| chr13:51776236 | T | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(196): Show |
251 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.363+824A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776236 | |||||||
| chr13:51776272 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.363+788G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776272 | |||||||
| chr13:51776273 | G | A | 44 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0038 others(41): Show |
60 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(57): Show |
intron_variant | MODIFIER | c.363+787C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776273 | |||||||
| chr13:51776281 | G | C | 67 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0038 others(64): Show |
87 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.363+779C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776281 | |||||||
| chr13:51776404 | C | T | 15 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0040 others(12): Show |
24 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.363+656G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776404 | |||||||
| chr13:51776405 | G | C | 60 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0038 others(57): Show |
80 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(77): Show |
intron_variant | MODIFIER | c.363+655C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776405 | |||||||
| chr13:51776453 | C | T | 1 | a0008c0009t0002g0311 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.363+607G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776453 | |||||||
| chr13:51776542 | T | C | 1 | a0001c0004t0001g0208 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.363+518A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776542 | |||||||
| chr13:51776684 | G | C | 2 | a0003c0003t0001g0220 a0003c0003t0001g0236 |
2 | HG00323.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.363+376C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776684 | |||||||
| chr13:51776853 | G | A | 8 | a0001c0001t0001g0075 a0001c0001t0001g0138 a0001c0001t0001g0234 others(5): Show |
8 | HG01975.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.363+207C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776853 | |||||||
| chr13:51776901 | C | T | 80 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0034 others(77): Show |
96 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.363+159G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776901 | |||||||
| chr13:51776965 | C | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0161 a0001c0001t0001g0177 others(1): Show |
5 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+95G>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 5/8 | chr13 | 51776965 | |||||||
| chr13:51777295 | C | T | 2 | a0001c0001t0003g0076 a0001c0001t0004g0064 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.302-174G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51777295 | |||||||
| chr13:51777366 | A | G | 1 | a0001c0001t0002g0285 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.302-245T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51777366 | |||||||
| chr13:51777599 | T | C | 1 | a0002c0002t0003g0159 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.302-478A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51777599 | |||||||
| chr13:51777923 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.302-802G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51777923 | |||||||
| chr13:51777996 | T | C | 178 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(175): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.302-875A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51777996 | |||||||
| chr13:51778047 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.302-926G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51778047 | |||||||
| chr13:51778118 | G | A | 32 | a0001c0001t0001g0142 a0001c0001t0002g0319 a0001c0001t0003g0259 others(29): Show |
41 | HG00735.hp1 HG01106.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.302-997C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51778118 | |||||||
| chr13:51778165 | G | A | 5 | a0001c0001t0001g0150 a0001c0001t0001g0161 a0001c0001t0001g0177 others(2): Show |
6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.302-1044C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51778165 | |||||||
| chr13:51778326 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.302-1205C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51778326 | |||||||
| chr13:51778579 | C | T | 1 | a0002c0002t0003g0232 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.302-1458G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51778579 | |||||||
| chr13:51778580 | G | A | 6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.302-1459C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51778580 | |||||||
| chr13:51778824 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.302-1703C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51778824 | |||||||
| chr13:51778889 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.302-1768C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51778889 | |||||||
| chr13:51778897 | G | A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0100 a0001c0001t0001g0119 |
3 | NA18951.hp2 NA18974.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.302-1776C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51778897 | |||||||
| chr13:51779001 | A | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.302-1880T>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51779001 | |||||||
| chr13:51779261 | T | C | 1 | a0003c0003t0001g0239 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.302-2140A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51779261 | |||||||
| chr13:51779635 | G | A | 1 | a0001c0001t0004g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.302-2514C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51779635 | |||||||
| chr13:51779817 | A | G | 3 | a0001c0001t0001g0071 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02809.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.302-2696T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51779817 | |||||||
| chr13:51779860 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.302-2739G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51779860 | |||||||
| chr13:51779952 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0125 a0001c0001t0004g0065 others(1): Show |
5 | HG01891.hp2 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.302-2831C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51779952 | |||||||
| chr13:51780056 | A | G | 1 | a0003c0003t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.302-2935T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51780056 | |||||||
| chr13:51780178 | A | AAAAT | 69 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(66): Show |
93 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.302-3061_302-3058d others(6): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51780178 | |||||||
| chr13:51780178 | A | AAAATAAA others(1): Show |
4 | a0001c0001t0001g0082 a0001c0001t0001g0094 a0001c0001t0001g0096 others(1): Show |
4 | HG00280.hp1 HG02165.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.302-3065_302-3058d others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51780178 | |||||||
| chr13:51780311 | C | G | 1 | a0002c0002t0003g0251 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.302-3190G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51780311 | |||||||
| chr13:51780334 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0096 |
3 | NA18971.hp1 NA19009.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.302-3213T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51780334 | |||||||
| chr13:51780355 | G | A | 4 | a0001c0001t0001g0168 a0001c0001t0001g0186 a0001c0001t0002g0001 others(1): Show |
10 | HG02074.hp1 NA18943.hp1 NA18965.hp2 others(7): Show |
intron_variant | MODIFIER | c.302-3234C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51780355 | |||||||
| chr13:51780430 | G | C | 1 | a0001c0001t0002g0323 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.302-3309C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51780430 | |||||||
| chr13:51780549 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.302-3428C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51780549 | |||||||
| chr13:51780633 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.302-3512G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51780633 | |||||||
| chr13:51781008 | C | G | 2 | a0001c0001t0001g0128 a0001c0001t0008g0328 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.302-3887G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51781008 | |||||||
| chr13:51781301 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0197 |
3 | HG00597.hp2 HG00609.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.302-4180C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51781301 | |||||||
| chr13:51781354 | ATCCAGT | A | 19 | a0001c0001t0001g0025 a0001c0001t0001g0036 a0001c0001t0001g0037 others(16): Show |
23 | HG00597.hp2 HG00609.hp2 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.302-4239_302-4234d others(8): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51781354 | |||||||
| chr13:51781366 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.302-4245C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51781366 | |||||||
| chr13:51781377 | G | A | 4 | a0001c0001t0002g0265 a0001c0001t0002g0308 a0001c0001t0002g0314 others(1): Show |
4 | HG00741.hp1 HG01981.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-4256C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51781377 | |||||||
| chr13:51781447 | G | A | 5 | a0001c0001t0001g0034 a0002c0002t0001g0191 a0002c0002t0003g0157 others(2): Show |
6 | HG01069.hp2 HG01071.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.302-4326C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51781447 | |||||||
| chr13:51781466 | C | A | 6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.302-4345G>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51781466 | |||||||
| chr13:51781467 | A | T | 6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.302-4346T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51781467 | |||||||
| chr13:51781488 | G | A | 1 | a0003c0003t0002g0201 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.302-4367C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51781488 | |||||||
| chr13:51781551 | C | T | 1 | a0005c0005t0001g0200 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.302-4430G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51781551 | |||||||
| chr13:51781653 | G | C | 1 | a0002c0002t0003g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.302-4532C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51781653 | |||||||
| chr13:51781698 | G | C | 1 | a0001c0001t0004g0007 | 3 | HG02109.hp1 HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.302-4577C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51781698 | |||||||
| chr13:51781729 | C | T | 8 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0125 others(5): Show |
10 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.302-4608G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51781729 | |||||||
| chr13:51781765 | T | C | 3 | a0001c0001t0001g0177 a0002c0002t0003g0176 a0002c0002t0006g0063 |
3 | HG02257.hp2 HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.302-4644A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51781765 | |||||||
| chr13:51781795 | G | A | 1 | a0001c0001t0002g0298 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.302-4674C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51781795 | |||||||
| chr13:51781951 | CTGCAGTG others(3): Show |
C | 1 | a0001c0001t0001g0325 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.302-4840_302-4831d others(12): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51781951 | |||||||
| chr13:51781952 | T | C | 297 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(294): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.302-4831A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51781952 | |||||||
| chr13:51781962 | T | C | 1 | a0001c0001t0001g0325 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.302-4841A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51781962 | |||||||
| chr13:51782088 | C | T | 1 | a0001c0001t0002g0303 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.302-4967G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51782088 | |||||||
| chr13:51782112 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.302-4991A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51782112 | |||||||
| chr13:51782270 | A | T | 106 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0026 others(103): Show |
133 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.302-5149T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51782270 | |||||||
| chr13:51782307 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.302-5186C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51782307 | |||||||
| chr13:51782429 | A | T | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.302-5308T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51782429 | |||||||
| chr13:51782432 | G | A | 1 | a0003c0003t0001g0221 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.302-5311C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51782432 | |||||||
| chr13:51782489 | C | T | 1 | a0001c0001t0002g0261 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.302-5368G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51782489 | |||||||
| chr13:51782564 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0125 |
5 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-5443G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51782564 | |||||||
| chr13:51782625 | T | C | 1 | a0001c0001t0004g0007 | 3 | HG02109.hp1 HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.302-5504A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51782625 | |||||||
| chr13:51782632 | C | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(108): Show |
150 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.302-5511G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51782632 | |||||||
| chr13:51782699 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.302-5578C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51782699 | |||||||
| chr13:51782818 | T | C | 1 | a0001c0001t0008g0328 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.302-5697A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51782818 | |||||||
| chr13:51782842 | T | G | 1 | a0001c0001t0001g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.302-5721A>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51782842 | |||||||
| chr13:51782932 | C | T | 1 | a0002c0002t0001g0191 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.302-5811G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51782932 | |||||||
| chr13:51783044 | G | A | 125 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(122): Show |
164 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.302-5923C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51783044 | |||||||
| chr13:51783147 | T | A | 1 | a0002c0002t0003g0218 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.302-6026A>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51783147 | |||||||
| chr13:51783201 | C | T | 5 | a0002c0002t0003g0042 a0002c0002t0003g0154 a0002c0002t0003g0174 others(2): Show |
6 | HG01243.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.302-6080G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51783201 | |||||||
| chr13:51783313 | G | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0125 others(1): Show |
6 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.302-6192C>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51783313 | |||||||
| chr13:51783503 | G | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0040 |
4 | NA18939.hp1 NA18957.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.302-6382C>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51783503 | |||||||
| chr13:51783679 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0102 |
2 | HG00099.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.301+6332C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51783679 | |||||||
| chr13:51783680 | C | T | 1 | a0001c0001t0001g0051 | 2 | HG01074.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.301+6331G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51783680 | |||||||
| chr13:51783835 | C | T | 1 | a0002c0002t0001g0193 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.301+6176G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51783835 | |||||||
| chr13:51784049 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.301+5962G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51784049 | |||||||
| chr13:51784068 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
4 | HG01074.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+5943T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51784068 | |||||||
| chr13:51784078 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.301+5933C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51784078 | |||||||
| chr13:51784085 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.301+5926C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51784085 | |||||||
| chr13:51784227 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.301+5784G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51784227 | |||||||
| chr13:51784234 | A | C | 1 | a0001c0001t0002g0126 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.301+5777T>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51784234 | |||||||
| chr13:51784280 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0096 |
3 | NA18971.hp1 NA19009.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.301+5731C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51784280 | |||||||
| chr13:51784320 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.301+5691T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51784320 | |||||||
| chr13:51784345 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.301+5666C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51784345 | |||||||
| chr13:51784543 | G | T | 7 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(4): Show |
7 | HG02559.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.301+5468C>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51784543 | |||||||
| chr13:51784797 | G | A | 6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.301+5214C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51784797 | |||||||
| chr13:51784839 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0125 |
5 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+5172A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51784839 | |||||||
| chr13:51784954 | G | A | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG00621.hp1 HG01346.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.301+5057C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51784954 | |||||||
| chr13:51785012 | G | C | 1 | a0001c0001t0001g0181 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.301+4999C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51785012 | |||||||
| chr13:51785017 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.301+4994G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51785017 | |||||||
| chr13:51785086 | G | T | 1 | a0001c0001t0003g0259 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.301+4925C>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51785086 | |||||||
| chr13:51785117 | A | T | 4 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | NA18950.hp2 NA18982.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+4894T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51785117 | |||||||
| chr13:51785134 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.301+4877T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51785134 | |||||||
| chr13:51785296 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.301+4715T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51785296 | |||||||
| chr13:51785341 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.301+4670A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51785341 | |||||||
| chr13:51785343 | T | TA | 7 | a0001c0001t0001g0058 a0001c0001t0001g0274 a0001c0001t0001g0291 others(4): Show |
8 | HG00438.hp2 NA18944.hp1 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.301+4667dupT | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51785343 | |||||||
| chr13:51785364 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.301+4647C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51785364 | |||||||
| chr13:51785425 | C | A | 1 | a0001c0001t0001g0128 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.301+4586G>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51785425 | |||||||
| chr13:51785573 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.301+4438C>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51785573 | |||||||
| chr13:51785633 | T | G | 219 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0013 others(216): Show |
272 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.301+4378A>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51785633 | |||||||
| chr13:51785901 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.301+4110A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51785901 | |||||||
| chr13:51786006 | A | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0068 others(4): Show |
10 | HG00423.hp1 NA18612.hp1 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.301+4005T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51786006 | |||||||
| chr13:51786094 | C | T | 1 | a0002c0002t0003g0324 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.301+3917G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51786094 | |||||||
| chr13:51786163 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.301+3848G>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51786163 | |||||||
| chr13:51786278 | T | C | 291 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(288): Show |
373 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.301+3733A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51786278 | |||||||
| chr13:51786322 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.301+3689G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51786322 | |||||||
| chr13:51786585 | A | C | 1 | a0001c0001t0001g0142 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.301+3426T>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51786585 | |||||||
| chr13:51786604 | G | A | 1 | a0001c0001t0004g0007 | 3 | HG02109.hp1 HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.301+3407C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51786604 | |||||||
| chr13:51786749 | G | A | 1 | a0001c0001t0008g0328 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.301+3262C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51786749 | |||||||
| chr13:51786760 | C | T | 1 | a0002c0002t0003g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.301+3251G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51786760 | |||||||
| chr13:51786817 | G | C | 1 | a0002c0002t0003g0232 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.301+3194C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51786817 | |||||||
| chr13:51786995 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.301+3016T>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51786995 | |||||||
| chr13:51787127 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG03927.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.301+2884G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787127 | |||||||
| chr13:51787139 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.301+2872G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787139 | |||||||
| chr13:51787314 | C | G | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02145.hp1 HG02572.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.301+2697G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787314 | |||||||
| chr13:51787328 | G | A | 1 | a0001c0001t0004g0065 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.301+2683C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787328 | |||||||
| chr13:51787725 | T | C | 9 | a0001c0001t0001g0035 a0001c0001t0001g0146 a0001c0001t0001g0147 others(6): Show |
10 | HG01192.hp2 HG01884.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.301+2286A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787725 | |||||||
| chr13:51787751 | TTTTA | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
172 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.301+2256_301+2259d others(6): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787751 | |||||||
| chr13:51787755 | ATATATAA others(1): Show |
A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0149 |
4 | NA18960.hp2 NA18963.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+2248_301+2255d others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787755 | |||||||
| chr13:51787797 | T | TAATATAT others(1): Show |
141 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(138): Show |
186 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.301+2213_301+2214i others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787797 | |||||||
| chr13:51787797 | T | TATATA | 153 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(150): Show |
187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.301+2209_301+2213d others(7): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787797 | |||||||
| chr13:51787842 | T | TAATATAT others(18): Show |
1 | a0001c0001t0001g0271 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.301+2144_301+2168d others(27): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787842 | |||||||
| chr13:51787868 | A | AAT | 197 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0013 others(194): Show |
247 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.301+2141_301+2142d others(4): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787868 | |||||||
| chr13:51787902 | A | AATTATAT | 5 | a0001c0001t0001g0026 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
9 | NA18971.hp1 NA18972.hp1 NA19001.hp1 others(6): Show |
intron_variant | MODIFIER | c.301+2108_301+2109i others(9): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787902 | |||||||
| chr13:51787902 | A | AATTATAT others(27): Show |
1 | a0001c0001t0001g0094 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.301+2108_301+2109i others(36): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787902 | |||||||
| chr13:51787903 | A | T | 1 | a0001c0001t0001g0301 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.301+2108T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787903 | |||||||
| chr13:51787904 | A | T | 6 | a0001c0001t0001g0026 a0001c0001t0001g0094 a0001c0001t0001g0095 others(3): Show |
10 | NA18971.hp1 NA18972.hp1 NA19001.hp1 others(7): Show |
intron_variant | MODIFIER | c.301+2107T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787904 | |||||||
| chr13:51787914 | T | A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0094 a0001c0001t0001g0095 others(3): Show |
10 | NA18971.hp1 NA18972.hp1 NA19001.hp1 others(7): Show |
intron_variant | MODIFIER | c.301+2097A>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787914 | |||||||
| chr13:51787920 | ATAATATA others(7): Show |
A | 1 | a0002c0002t0003g0189 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.301+2077_301+2090d others(16): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787920 | |||||||
| chr13:51787921 | T | TAAA | 6 | a0001c0001t0001g0026 a0001c0001t0001g0094 a0001c0001t0001g0095 others(3): Show |
10 | NA18971.hp1 NA18972.hp1 NA19001.hp1 others(7): Show |
intron_variant | MODIFIER | c.301+2089_301+2090i others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787921 | |||||||
| chr13:51787922 | AATATATA others(5): Show |
A | 179 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0013 others(176): Show |
222 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.301+2077_301+2088d others(14): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787922 | |||||||
| chr13:51787930 | C | A | 9 | a0001c0001t0001g0026 a0001c0001t0001g0094 a0001c0001t0001g0095 others(6): Show |
13 | HG02145.hp1 HG03041.hp2 HG03540.hp2 others(10): Show |
intron_variant | MODIFIER | c.301+2081G>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787930 | |||||||
| chr13:51787934 | T | TATATA | 6 | a0001c0001t0001g0026 a0001c0001t0001g0094 a0001c0001t0001g0095 others(3): Show |
10 | NA18971.hp1 NA18972.hp1 NA19001.hp1 others(7): Show |
intron_variant | MODIFIER | c.301+2072_301+2076d others(7): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51787934 | |||||||
| chr13:51788092 | C | G | 7 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(4): Show |
9 | HG02109.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.301+1919G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51788092 | |||||||
| chr13:51788096 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.301+1915G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51788096 | |||||||
| chr13:51788156 | G | C | 1 | a0001c0001t0001g0023 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.301+1855C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51788156 | |||||||
| chr13:51788222 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.301+1789C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51788222 | |||||||
| chr13:51788344 | G | C | 9 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0167 others(6): Show |
17 | NA18939.hp1 NA18943.hp1 NA18953.hp2 others(14): Show |
intron_variant | MODIFIER | c.301+1667C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51788344 | |||||||
| chr13:51788413 | A | G | 3 | a0001c0001t0004g0021 a0001c0001t0004g0065 a0001c0001t0004g0066 |
4 | HG02896.hp2 HG02897.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+1598T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51788413 | |||||||
| chr13:51788570 | C | T | 5 | a0003c0003t0001g0045 a0003c0003t0001g0220 a0003c0003t0001g0235 others(2): Show |
6 | HG00323.hp2 HG01081.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.301+1441G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51788570 | |||||||
| chr13:51788599 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.301+1412G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51788599 | |||||||
| chr13:51788792 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(204): Show |
267 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.301+1219A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51788792 | |||||||
| chr13:51788859 | C | CA | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(9): Show |
13 | HG02145.hp1 HG02257.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.301+1151dupT | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51788859 | |||||||
| chr13:51789199 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.301+812A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51789199 | |||||||
| chr13:51789275 | A | C | 19 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0089 others(16): Show |
22 | HG00408.hp1 HG00438.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.301+736T>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51789275 | |||||||
| chr13:51789354 | G | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0013 others(23): Show |
39 | HG00423.hp1 HG01069.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.301+657C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51789354 | |||||||
| chr13:51789383 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.301+628G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51789383 | |||||||
| chr13:51789623 | C | T | 2 | a0001c0001t0001g0177 a0002c0002t0003g0176 |
2 | HG02257.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.301+388G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51789623 | |||||||
| chr13:51789667 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.301+344C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51789667 | |||||||
| chr13:51789757 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.301+254T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51789757 | |||||||
| chr13:51789896 | C | T | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02145.hp1 HG02572.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.301+115G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 4/8 | chr13 | 51789896 | |||||||
| chr13:51790167 | C | A | 4 | a0001c0001t0001g0322 a0001c0001t0002g0061 a0001c0001t0002g0323 others(1): Show |
5 | HG03491.hp2 HG03492.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-75G>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 3/8 | chr13 | 51790167 | |||||||
| chr13:51790224 | G | T | 4 | a0001c0001t0001g0322 a0001c0001t0002g0061 a0001c0001t0002g0323 others(1): Show |
5 | HG03491.hp2 HG03492.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-132C>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 3/8 | chr13 | 51790224 | |||||||
| chr13:51790484 | T | C | 2 | a0001c0001t0001g0282 a0002c0002t0003g0050 |
3 | HG01081.hp2 HG01109.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.220-392A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 3/8 | chr13 | 51790484 | |||||||
| chr13:51790506 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.220-414A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 3/8 | chr13 | 51790506 | |||||||
| chr13:51790569 | C | A | 1 | a0001c0001t0001g0054 | 2 | HG00738.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.220-477G>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 3/8 | chr13 | 51790569 | |||||||
| chr13:51790681 | G | A | 1 | a0001c0001t0004g0065 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.219+484C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 3/8 | chr13 | 51790681 | |||||||
| chr13:51790756 | C | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.219+409G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 3/8 | chr13 | 51790756 | |||||||
| chr13:51790777 | T | C | 1 | a0001c0001t0001g0008 | 3 | HG01074.hp1 HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.219+388A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 3/8 | chr13 | 51790777 | |||||||
| chr13:51790885 | A | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(95): Show |
130 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.219+280T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 3/8 | chr13 | 51790885 | |||||||
| chr13:51790895 | C | A | 1 | a0002c0002t0003g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.219+270G>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 3/8 | chr13 | 51790895 | |||||||
| chr13:51790926 | T | A | 1 | a0001c0001t0001g0103 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.219+239A>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 3/8 | chr13 | 51790926 | |||||||
| chr13:51791049 | G | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(88): Show |
123 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.219+116C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 3/8 | chr13 | 51791049 | |||||||
| chr13:51791097 | T | A | 1 | a0001c0001t0001g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.219+68A>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 3/8 | chr13 | 51791097 | |||||||
| chr13:51791271 | C | CA | 5 | a0001c0001t0001g0057 a0001c0001t0001g0128 a0001c0001t0001g0188 others(2): Show |
6 | HG00280.hp2 HG01496.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-15dupT | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51791271 | |||||||
| chr13:51791271 | CA | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(84): Show |
120 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.127-15delT | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51791271 | |||||||
| chr13:51791285 | A | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0216 |
4 | HG01074.hp1 HG01243.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-28T>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51791285 | |||||||
| chr13:51791380 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.127-123A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51791380 | |||||||
| chr13:51791387 | C | A | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0013 others(122): Show |
163 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.127-130G>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51791387 | |||||||
| chr13:51791567 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.127-310G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51791567 | |||||||
| chr13:51791687 | A | G | 85 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
117 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.127-430T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51791687 | |||||||
| chr13:51791824 | G | C | 1 | a0001c0001t0001g0272 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.127-567C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51791824 | |||||||
| chr13:51792340 | TGAC | T | 6 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0150 others(3): Show |
6 | HG01884.hp1 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-1086_127-1084d others(5): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51792340 | |||||||
| chr13:51792478 | C | A | 6 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0150 others(3): Show |
6 | HG01884.hp1 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-1221G>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51792478 | |||||||
| chr13:51792588 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.127-1331G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51792588 | |||||||
| chr13:51792643 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.127-1386C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51792643 | |||||||
| chr13:51792767 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.127-1510G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51792767 | |||||||
| chr13:51792784 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127-1527C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51792784 | |||||||
| chr13:51792898 | TG | T | 4 | a0001c0001t0001g0322 a0001c0001t0002g0061 a0001c0001t0002g0323 others(1): Show |
5 | HG03491.hp2 HG03492.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-1642delC | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51792898 | |||||||
| chr13:51792919 | C | A | 1 | a0001c0001t0001g0169 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.127-1662G>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51792919 | |||||||
| chr13:51793057 | G | C | 9 | a0001c0001t0002g0318 a0001c0001t0002g0319 a0001c0001t0003g0259 others(6): Show |
13 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.127-1800C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51793057 | |||||||
| chr13:51793071 | C | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
105 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.127-1814G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51793071 | |||||||
| chr13:51793172 | G | A | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0013 others(122): Show |
163 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.127-1915C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51793172 | |||||||
| chr13:51793363 | C | A | 27 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0013 others(24): Show |
41 | HG00423.hp1 HG01069.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.127-2106G>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51793363 | |||||||
| chr13:51793744 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.127-2487G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51793744 | |||||||
| chr13:51793886 | C | T | 1 | a0002c0002t0003g0159 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.127-2629G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51793886 | |||||||
| chr13:51793975 | C | G | 1 | a0002c0002t0003g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.127-2718G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51793975 | |||||||
| chr13:51794156 | G | A | 2 | a0001c0001t0001g0177 a0002c0002t0003g0176 |
2 | HG02257.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.127-2899C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51794156 | |||||||
| chr13:51794171 | G | A | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG02145.hp1 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.127-2914C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51794171 | |||||||
| chr13:51794354 | A | G | 1 | a0002c0002t0003g0249 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.127-3097T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51794354 | |||||||
| chr13:51794419 | G | A | 1 | a0007c0006t0004g0062 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.127-3162C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51794419 | |||||||
| chr13:51794475 | C | G | 5 | a0001c0001t0001g0322 a0001c0001t0001g0325 a0001c0001t0002g0061 others(2): Show |
6 | HG02451.hp2 HG03491.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-3218G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51794475 | |||||||
| chr13:51794756 | G | A | 1 | a0007c0006t0004g0062 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.127-3499C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51794756 | |||||||
| chr13:51794792 | GT | G | 246 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(243): Show |
305 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(302): Show |
intron_variant | MODIFIER | c.127-3536delA | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51794792 | |||||||
| chr13:51794835 | C | T | 5 | a0001c0001t0001g0322 a0001c0001t0001g0325 a0001c0001t0002g0061 others(2): Show |
6 | HG02451.hp2 HG03491.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-3578G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51794835 | |||||||
| chr13:51794845 | G | A | 1 | a0002c0002t0003g0232 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.127-3588C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51794845 | |||||||
| chr13:51794855 | C | G | 311 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(308): Show |
401 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(398): Show |
intron_variant | MODIFIER | c.127-3598G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51794855 | |||||||
| chr13:51794906 | G | A | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.127-3649C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51794906 | |||||||
| chr13:51794939 | C | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG02145.hp1 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.127-3682G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51794939 | |||||||
| chr13:51794987 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.127-3730A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51794987 | |||||||
| chr13:51795006 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.127-3749G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51795006 | |||||||
| chr13:51795033 | A | G | 4 | a0001c0001t0001g0322 a0001c0001t0002g0061 a0001c0001t0002g0323 others(1): Show |
5 | HG03491.hp2 HG03492.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-3776T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51795033 | |||||||
| chr13:51795163 | G | A | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG02145.hp1 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.127-3906C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51795163 | |||||||
| chr13:51795228 | C | G | 260 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(257): Show |
330 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.127-3971G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51795228 | |||||||
| chr13:51795292 | T | G | 1 | a0001c0004t0001g0208 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.127-4035A>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51795292 | |||||||
| chr13:51795757 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0003g0076 |
2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.126+3777G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51795757 | |||||||
| chr13:51795803 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.126+3731G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51795803 | |||||||
| chr13:51795870 | T | G | 1 | a0002c0002t0003g0189 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.126+3664A>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51795870 | |||||||
| chr13:51796258 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.126+3276T>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51796258 | |||||||
| chr13:51796764 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.126+2770G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51796764 | |||||||
| chr13:51796777 | G | A | 1 | a0001c0001t0002g0260 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.126+2757C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51796777 | |||||||
| chr13:51797097 | G | T | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | HG02145.hp1 HG02572.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+2437C>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51797097 | |||||||
| chr13:51797185 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.126+2349T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51797185 | |||||||
| chr13:51797257 | T | A | 3 | a0003c0003t0005g0241 a0003c0003t0005g0242 a0003c0003t0005g0243 |
3 | NA18979.hp2 NA18993.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.126+2277A>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51797257 | |||||||
| chr13:51797396 | G | A | 15 | a0001c0001t0001g0029 a0001c0001t0001g0135 a0001c0001t0001g0136 others(12): Show |
19 | HG02109.hp1 HG02145.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.126+2138C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51797396 | |||||||
| chr13:51797435 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.126+2099C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51797435 | |||||||
| chr13:51797579 | C | T | 4 | a0001c0001t0001g0068 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | NA19004.hp1 NA19010.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+1955G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51797579 | |||||||
| chr13:51797618 | G | A | 91 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(88): Show |
123 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.126+1916C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51797618 | |||||||
| chr13:51797837 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.126+1697A>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51797837 | |||||||
| chr13:51797843 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0105 a0001c0001t0001g0123 |
4 | NA18957.hp2 NA18972.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+1691C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51797843 | |||||||
| chr13:51797991 | T | C | 4 | a0002c0002t0003g0017 a0002c0002t0003g0190 a0002c0002t0003g0217 others(1): Show |
6 | HG02055.hp1 HG02559.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+1543A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51797991 | |||||||
| chr13:51798027 | T | A | 2 | a0002c0002t0001g0191 a0002c0002t0003g0192 |
2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.126+1507A>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51798027 | |||||||
| chr13:51798038 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.126+1496G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51798038 | |||||||
| chr13:51798109 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.126+1425G>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51798109 | |||||||
| chr13:51798109 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.126+1425G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51798109 | |||||||
| chr13:51798249 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.126+1285A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51798249 | |||||||
| chr13:51798353 | A | G | 6 | a0001c0001t0001g0128 a0001c0001t0001g0135 a0001c0001t0001g0136 others(3): Show |
6 | HG02145.hp1 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+1181T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51798353 | |||||||
| chr13:51798393 | C | A | 1 | a0001c0001t0002g0283 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.126+1141G>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51798393 | |||||||
| chr13:51798663 | T | A | 2 | a0001c0001t0004g0007 a0007c0006t0004g0062 |
4 | HG02109.hp1 HG02280.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+871A>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51798663 | |||||||
| chr13:51798721 | TAGAG | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(74): Show |
106 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.126+809_126+812del others(4): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51798721 | |||||||
| chr13:51798729 | G | A | 47 | a0001c0001t0001g0015 a0001c0001t0001g0172 a0001c0001t0001g0173 others(44): Show |
57 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.126+805C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51798729 | |||||||
| chr13:51798883 | G | A | 6 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0325 others(3): Show |
7 | HG02451.hp2 HG02559.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+651C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51798883 | |||||||
| chr13:51798927 | T | G | 1 | a0002c0002t0003g0324 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.126+607A>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51798927 | |||||||
| chr13:51799061 | C | G | 3 | a0001c0001t0004g0021 a0001c0001t0004g0065 a0001c0001t0004g0066 |
4 | HG02896.hp2 HG02897.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+473G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51799061 | |||||||
| chr13:51799094 | C | T | 2 | a0001c0001t0001g0177 a0002c0002t0003g0176 |
2 | HG02257.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.126+440G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51799094 | |||||||
| chr13:51799115 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0149 |
4 | NA18960.hp2 NA18963.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+419G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51799115 | |||||||
| chr13:51799247 | T | G | 1 | a0001c0001t0001g0011 | 3 | HG01123.hp2 HG01192.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.126+287A>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51799247 | |||||||
| chr13:51799281 | A | T | 1 | a0001c0001t0007g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.126+253T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51799281 | |||||||
| chr13:51799302 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.126+232C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51799302 | |||||||
| chr13:51799400 | A | T | 1 | a0001c0001t0001g0081 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.126+134T>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 2/8 | chr13 | 51799400 | |||||||
| chr13:51799678 | G | C | 249 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0013 others(246): Show |
312 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.-8-11C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51799678 | |||||||
| chr13:51799993 | C | A | 3 | a0001c0001t0004g0021 a0001c0001t0004g0065 a0001c0001t0004g0066 |
4 | HG02896.hp2 HG02897.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-326G>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51799993 | |||||||
| chr13:51800056 | C | CAGG | 24 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0040 others(21): Show |
35 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-8-392_-8-390dupCC others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51800056 | |||||||
| chr13:51800109 | A | C | 1 | a0001c0001t0007g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-8-442T>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51800109 | |||||||
| chr13:51800353 | T | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
160 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.-8-686A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51800353 | |||||||
| chr13:51800469 | G | C | 1 | a0002c0002t0003g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-8-802C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51800469 | |||||||
| chr13:51800502 | C | G | 8 | a0001c0001t0002g0318 a0001c0001t0002g0319 a0002c0002t0003g0002 others(5): Show |
12 | HG00741.hp2 HG01106.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-8-835G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51800502 | |||||||
| chr13:51800541 | C | G | 2 | a0002c0002t0003g0072 a0002c0002t0003g0073 |
2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-8-874G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51800541 | |||||||
| chr13:51800710 | G | A | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG00621.hp1 HG01346.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-8-1043C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51800710 | |||||||
| chr13:51800888 | C | T | 1 | a0002c0002t0003g0244 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-8-1221G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51800888 | |||||||
| chr13:51800942 | A | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0173 a0002c0002t0003g0174 |
5 | HG02723.hp1 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1275T>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51800942 | |||||||
| chr13:51801064 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-8-1397G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51801064 | |||||||
| chr13:51801067 | A | G | 3 | a0001c0001t0002g0267 a0001c0001t0002g0285 a0001c0001t0002g0286 |
3 | HG02015.hp2 NA18973.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-8-1400T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51801067 | |||||||
| chr13:51801075 | A | G | 1 | a0001c0001t0002g0266 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-8-1408T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51801075 | |||||||
| chr13:51801130 | G | A | 37 | a0001c0001t0001g0015 a0001c0001t0001g0172 a0001c0001t0001g0173 others(34): Show |
45 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.-8-1463C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51801130 | |||||||
| chr13:51801247 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-8-1580G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51801247 | |||||||
| chr13:51801336 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-8-1669C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51801336 | |||||||
| chr13:51801364 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-8-1697A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51801364 | |||||||
| chr13:51801463 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0125 |
5 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-1796G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51801463 | |||||||
| chr13:51801465 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-8-1798C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51801465 | |||||||
| chr13:51801565 | A | C | 3 | a0002c0002t0003g0154 a0002c0002t0003g0175 a0002c0002t0003g0207 |
3 | HG02572.hp1 HG02615.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-8-1898T>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51801565 | |||||||
| chr13:51801647 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-8-1980G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51801647 | |||||||
| chr13:51801673 | C | T | 2 | a0001c0001t0004g0007 a0007c0006t0004g0062 |
4 | HG02109.hp1 HG02280.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-2006G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51801673 | |||||||
| chr13:51801674 | G | A | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | HG02145.hp1 HG02572.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-2007C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51801674 | |||||||
| chr13:51801717 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-8-2050C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51801717 | |||||||
| chr13:51801785 | AG | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0173 a0002c0002t0003g0174 |
5 | HG02723.hp1 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-2119delC | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51801785 | |||||||
| chr13:51801870 | C | T | 7 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0130 others(4): Show |
7 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+2184G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51801870 | |||||||
| chr13:51801891 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-9+2163C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51801891 | |||||||
| chr13:51801975 | G | C | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-9+2079C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51801975 | |||||||
| chr13:51802048 | G | C | 1 | a0002c0002t0003g0244 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-9+2006C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802048 | |||||||
| chr13:51802169 | T | TCA | 9 | a0001c0001t0001g0048 a0001c0001t0001g0245 a0001c0001t0001g0312 others(6): Show |
10 | HG01978.hp2 HG02486.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9+1883_-9+1884dup others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802169 | |||||||
| chr13:51802169 | T | TCACA | 2 | a0002c0002t0003g0049 a0002c0002t0003g0249 |
3 | HG01106.hp2 HG01255.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-9+1881_-9+1884dup others(4): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802169 | |||||||
| chr13:51802169 | T | TCACACA | 5 | a0001c0001t0001g0250 a0001c0001t0002g0315 a0002c0002t0003g0251 others(2): Show |
5 | HG01109.hp2 HG01515.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+1879_-9+1884dup others(6): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802169 | |||||||
| chr13:51802169 | TCA | T | 49 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0030 others(46): Show |
63 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-9+1883_-9+1884del others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802169 | |||||||
| chr13:51802169 | TCACA | T | 55 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0039 others(52): Show |
72 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.-9+1881_-9+1884del others(4): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802169 | |||||||
| chr13:51802169 | TCACACA | T | 37 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0033 others(34): Show |
47 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.-9+1879_-9+1884del others(6): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802169 | |||||||
| chr13:51802169 | TCACACAC others(1): Show |
T | 20 | a0001c0001t0001g0013 a0001c0001t0001g0031 a0001c0001t0001g0055 others(17): Show |
31 | HG00280.hp2 HG00735.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.-9+1877_-9+1884del others(8): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802169 | |||||||
| chr13:51802169 | TCACACAC others(3): Show |
T | 20 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0054 others(17): Show |
25 | HG00099.hp1 HG00558.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.-9+1875_-9+1884del others(10): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802169 | |||||||
| chr13:51802169 | TCACACAC others(5): Show |
T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0147 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-9+1873_-9+1884del others(12): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802169 | |||||||
| chr13:51802169 | TCACACAC others(7): Show |
T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0146 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-9+1871_-9+1884del others(14): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802169 | |||||||
| chr13:51802169 | TCACACAC others(9): Show |
T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0144 a0003c0003t0001g0145 |
3 | HG00597.hp1 HG02132.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-9+1869_-9+1884del others(16): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802169 | |||||||
| chr13:51802169 | TCACACAC others(11): Show |
T | 1 | a0002c0002t0003g0050 | 2 | HG01081.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.-9+1867_-9+1884del others(18): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802169 | |||||||
| chr13:51802169 | TCACACAC others(15): Show |
T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0321 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-9+1863_-9+1884del others(22): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802169 | |||||||
| chr13:51802169 | TCACACAC others(25): Show |
T | 1 | a0001c0001t0001g0142 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-9+1853_-9+1884del others(32): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802169 | |||||||
| chr13:51802199 | ACACACAC others(12): Show |
A | 1 | a0002c0002t0006g0063 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-9+1836_-9+1854del others(19): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802199 | |||||||
| chr13:51802201 | ACACACAC others(10): Show |
A | 5 | a0001c0001t0001g0071 a0001c0001t0001g0135 a0001c0001t0001g0136 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+1836_-9+1852del others(17): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802201 | |||||||
| chr13:51802205 | ACACACAC others(6): Show |
A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0075 others(10): Show |
20 | HG00741.hp2 HG01074.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.-9+1836_-9+1848del others(13): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802205 | |||||||
| chr13:51802207 | ACACACAC others(4): Show |
A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(38): Show |
58 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.-9+1836_-9+1846del others(11): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802207 | |||||||
| chr13:51802209 | ACACACAC others(2): Show |
A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0111 a0001c0001t0001g0112 others(2): Show |
6 | HG02056.hp1 HG03927.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+1836_-9+1844del others(9): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802209 | |||||||
| chr13:51802210 | C | G | 1 | a0002c0002t0003g0141 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-9+1844G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802210 | |||||||
| chr13:51802211 | ACACACAC | A | 11 | a0001c0001t0001g0012 a0001c0001t0001g0115 a0001c0001t0001g0116 others(8): Show |
13 | NA18612.hp1 NA18747.hp2 NA18964.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9+1836_-9+1842del others(7): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802211 | |||||||
| chr13:51802218 | C | CA | 3 | a0001c0001t0001g0125 a0001c0001t0001g0138 a0001c0001t0002g0126 |
3 | HG00642.hp1 HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-9+1835_-9+1836ins others(1): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802218 | |||||||
| chr13:51802350 | G | C | 81 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0030 others(78): Show |
99 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.-9+1704C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802350 | |||||||
| chr13:51802393 | T | C | 1 | a0001c0001t0001g0325 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-9+1661A>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802393 | |||||||
| chr13:51802447 | G | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
107 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.-9+1607C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802447 | |||||||
| chr13:51802497 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0139 a0001c0001t0001g0140 |
4 | NA18988.hp2 NA19000.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+1557G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802497 | |||||||
| chr13:51802648 | A | G | 8 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0325 others(5): Show |
11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9+1406T>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802648 | |||||||
| chr13:51802913 | TAC | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
107 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.-9+1139_-9+1140del others(2): Show |
DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51802913 | |||||||
| chr13:51803160 | C | T | 100 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(97): Show |
132 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-9+894G>A | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51803160 | |||||||
| chr13:51803236 | G | A | 1 | a0003c0003t0001g0316 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-9+818C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51803236 | |||||||
| chr13:51803376 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-9+678C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51803376 | |||||||
| chr13:51803401 | G | A | 3 | a0001c0001t0002g0318 a0001c0001t0002g0319 a0002c0002t0003g0320 |
3 | HG00741.hp2 HG01106.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.-9+653C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51803401 | |||||||
| chr13:51803520 | G | A | 6 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0325 others(3): Show |
7 | HG02451.hp2 HG02559.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+534C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51803520 | |||||||
| chr13:51803906 | G | A | 1 | a0001c0001t0003g0326 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-9+148C>T | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51803906 | |||||||
| chr13:51804006 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-9+48G>C | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51804006 | |||||||
| chr13:51804008 | G | C | 1 | a0003c0003t0001g0327 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-9+46C>G | DHRS12 | ENSG00000102796.12 | transcript | ENST00000444610.8 | protein_coding | 1/8 | chr13 | 51804008 |