Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1634 |
| ensemblid | ENSG00000011465.18 |
| hgncid | 2705 |
| symbol | DCN |
| name | decorin |
| refseq_nuc | NM_001920.5 |
| refseq_prot | NP_001911.1 |
| ensembl_nuc | ENST00000052754.10 |
| ensembl_prot | ENSP00000052754.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 91140484 |
| end | 91182817 |
| strand | - |
| ver | v1.2 |
| region | chr12:91140484-91182817 |
| region5000 | chr12:91135484-91187817 |
| regionname0 | DCN_chr12_91140484_91182817 |
| regionname5000 | DCN_chr12_91135484_91187817 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 359 | 222 | 71 | 39 | 88 | 4 | 18 | 70 | DCN_chr12_91135484_91187817 | DCN | MKATI others(354): Show |
chr12 | 91135484 | 91187817 |
| a0002 | 0/0 | 359 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | MKATI others(354): Show |
chr12 | 91135484 | 91187817 |
| a0003 | 0/0 | 359 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | MKATI others(354): Show |
chr12 | 91135484 | 91187817 |
| a0004 | 0/0 | 359 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | MKATI others(354): Show |
chr12 | 91135484 | 91187817 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1077 | 217 | 67 | 38 | 88 | 4 | 18 | DCN_chr12_91135484_91187817 | DCN | ATGAA others(1072): Show |
chr12 | 91135484 | 91187817 | ||
| a0001c0003 | 0/0 | 1077 | 4 | 3 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | ATGAA others(1072): Show |
chr12 | 91135484 | 91187817 | ||
| a0001c0007 | 0/0 | 1077 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | ATGAA others(1072): Show |
chr12 | 91135484 | 91187817 | ||
| a0002c0002 | 0/0 | 1077 | 8 | 7 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | ATGAA others(1072): Show |
chr12 | 91135484 | 91187817 | ||
| a0002c0006 | 0/0 | 1077 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | ATGAA others(1072): Show |
chr12 | 91135484 | 91187817 | ||
| a0003c0004 | 0/0 | 1077 | 3 | 3 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | ATGAA others(1072): Show |
chr12 | 91135484 | 91187817 | ||
| a0004c0005 | 0/0 | 1077 | 2 | 0 | 2 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | ATGAA others(1072): Show |
chr12 | 91135484 | 91187817 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6850 | 127 | 23 | 25 | 63 | 3 | 11 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0002 | 0/0 | 6850 | 22 | 7 | 4 | 9 | 0 | 2 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0003 | 0/0 | 6850 | 12 | 12 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0004 | 0/0 | 6850 | 10 | 9 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0006 | 0/0 | 6850 | 8 | 0 | 1 | 7 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0007 | 0/0 | 6850 | 4 | 4 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0009 | 0/0 | 6850 | 3 | 1 | 0 | 0 | 0 | 2 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0010 | 0/0 | 6850 | 3 | 0 | 2 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0011 | 0/0 | 6850 | 3 | 3 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0012 | 0/0 | 6850 | 2 | 0 | 0 | 2 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0013 | 0/0 | 6850 | 2 | 0 | 0 | 2 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0014 | 0/0 | 6850 | 2 | 0 | 2 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0015 | 0/0 | 6850 | 2 | 2 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0016 | 0/0 | 6852 | 2 | 0 | 1 | 0 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6847): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0017 | 0/0 | 6850 | 2 | 2 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0018 | 0/0 | 6850 | 2 | 2 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0020 | 0/0 | 6850 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0022 | 0/0 | 6850 | 1 | 0 | 0 | 0 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0023 | 0/0 | 6850 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0024 | 0/0 | 6850 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0025 | 0/0 | 6850 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0026 | 0/0 | 6850 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0027 | 0/0 | 6850 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0028 | 0/0 | 6850 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0029 | 0/0 | 6850 | 1 | 0 | 0 | 0 | 1 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0030 | 0/0 | 6850 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0001t0031 | 0/0 | 6850 | 1 | 0 | 0 | 0 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0003t0008 | 0/0 | 6850 | 3 | 3 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0003t0021 | 0/0 | 6850 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0001c0007t0001 | 0/0 | 6850 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0002c0002t0005 | 0/0 | 6851 | 8 | 7 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6846): Show |
chr12 | 91135484 | 91187817 |
| a0002c0006t0005 | 0/0 | 6851 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6846): Show |
chr12 | 91135484 | 91187817 |
| a0003c0004t0001 | 0/0 | 6850 | 3 | 3 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| a0004c0005t0019 | 0/0 | 6850 | 2 | 0 | 2 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | AACTG others(6845): Show |
chr12 | 91135484 | 91187817 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0006g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0007g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0009g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0009g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0009g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0010g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0010g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0010g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0011g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0011g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0012g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0012g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0013g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0013g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0014g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0015g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0015g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0016g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0016g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0017g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0017g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0018g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0018g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0020g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0022g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0023g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0024g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0025g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0026g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0027g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0028g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0029g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0030g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0001t0031g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0003t0008g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0003t0021g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0001c0007t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0002c0002t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0002c0002t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0002c0002t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0002c0002t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0002c0002t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0002c0002t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0002c0002t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0002c0002t0005g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0002c0006t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0003c0004t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0003c0004t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0003c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0004c0005t0019g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| a0004c0005t0019g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0029 | g0075 | EUR | GBR | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | GBR | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG00609 | hp1 | a0001 | c0001 | t0030 | g0065 | EAS | CHS | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG00639 | hp1 | a0001 | c0001 | t0025 | g0179 | AMR | PUR | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG00733 | hp2 | a0001 | c0001 | t0014 | g0011 | AMR | PUR | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0210 | AMR | PUR | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01192 | hp2 | a0001 | c0003 | t0021 | g0204 | AMR | PUR | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01243 | hp1 | a0001 | c0001 | t0014 | g0011 | AMR | PUR | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01255 | hp2 | a0001 | c0001 | t0010 | g0107 | AMR | CLM | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01256 | hp1 | a0001 | c0001 | t0016 | g0081 | AMR | CLM | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01358 | hp1 | a0001 | c0001 | t0010 | g0111 | AMR | CLM | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01433 | hp2 | a0002 | c0002 | t0005 | g0200 | AMR | CLM | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01891 | hp2 | a0001 | c0007 | t0001 | g0205 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01934 | hp1 | a0004 | c0005 | t0019 | g0127 | AMR | PEL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01993 | hp2 | a0001 | c0001 | t0023 | g0108 | AMR | PEL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02129 | hp1 | a0001 | c0001 | t0012 | g0129 | EAS | KHV | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02145 | hp1 | a0001 | c0001 | t0011 | g0047 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02165 | hp1 | a0001 | c0001 | t0012 | g0164 | EAS | CDX | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02165 | hp2 | a0001 | c0001 | t0010 | g0100 | EAS | CDX | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02258 | hp1 | a0001 | c0001 | t0018 | g0042 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02258 | hp2 | a0001 | c0003 | t0008 | g0004 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02273 | hp1 | a0001 | c0001 | t0006 | g0036 | AMR | PEL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0211 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0046 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02451 | hp2 | a0001 | c0001 | t0017 | g0186 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0214 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02602 | hp1 | a0001 | c0001 | t0031 | g0125 | SAS | PJL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02615 | hp1 | a0002 | c0006 | t0005 | g0192 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0207 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0213 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02622 | hp2 | a0002 | c0002 | t0005 | g0193 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0174 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02717 | hp2 | a0002 | c0002 | t0005 | g0194 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02735 | hp2 | a0001 | c0001 | t0016 | g0082 | SAS | PJL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02886 | hp2 | a0001 | c0001 | t0011 | g0049 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02895 | hp2 | a0001 | c0001 | t0015 | g0203 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02896 | hp1 | a0002 | c0002 | t0005 | g0198 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02965 | hp1 | a0001 | c0001 | t0015 | g0202 | AFR | ESN | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02965 | hp2 | a0001 | c0003 | t0008 | g0004 | AFR | ESN | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0212 | AFR | ESN | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02976 | hp2 | a0003 | c0004 | t0001 | g0157 | AFR | ESN | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0201 | AFR | GWD | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | MSL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | MSL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03130 | hp1 | a0003 | c0004 | t0001 | g0022 | AFR | ESN | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03130 | hp2 | a0001 | c0001 | t0017 | g0185 | AFR | ESN | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03139 | hp1 | a0001 | c0001 | t0018 | g0043 | AFR | ESN | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | ESN | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | ESN | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0206 | AFR | MSL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03209 | hp2 | a0002 | c0002 | t0005 | g0197 | AFR | MSL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | MSL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | MSL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | MSL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03491 | hp2 | a0001 | c0001 | t0009 | g0159 | SAS | PJL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03492 | hp1 | a0001 | c0001 | t0009 | g0182 | SAS | PJL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03492 | hp2 | a0001 | c0001 | t0022 | g0139 | SAS | PJL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03516 | hp1 | a0001 | c0001 | t0020 | g0019 | AFR | ESN | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | ESN | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | MSL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | MSL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | YRI | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | YRI | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18941 | hp2 | a0001 | c0001 | t0026 | g0103 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18965 | hp2 | a0001 | c0001 | t0013 | g0134 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18968 | hp1 | a0001 | c0001 | t0006 | g0031 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18970 | hp2 | a0001 | c0001 | t0006 | g0034 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18975 | hp1 | a0001 | c0001 | t0006 | g0039 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18992 | hp1 | a0001 | c0001 | t0006 | g0041 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19005 | hp2 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19007 | hp1 | a0001 | c0001 | t0013 | g0137 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0037 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19030 | hp1 | a0002 | c0002 | t0005 | g0196 | AFR | LWK | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0190 | AFR | LWK | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19043 | hp1 | a0001 | c0003 | t0008 | g0004 | AFR | LWK | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0018 | AFR | LWK | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19072 | hp2 | a0001 | c0001 | t0006 | g0032 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19076 | hp2 | a0001 | c0001 | t0028 | g0123 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19090 | hp1 | a0001 | c0001 | t0027 | g0121 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | YRI | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA19240 | hp2 | a0003 | c0004 | t0001 | g0021 | AFR | YRI | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA20129 | hp1 | a0001 | c0001 | t0024 | g0181 | AFR | ASW | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA20129 | hp2 | a0002 | c0002 | t0005 | g0199 | AFR | ASW | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | TSI | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | TSI | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01123 | hp1 | a0004 | c0005 | t0019 | g0149 | AMR | CLM | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0209 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02559 | hp1 | a0002 | c0002 | t0005 | g0195 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | USA | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0208 | AFR | USA | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | LWK | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0128 | REF | REF | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0165 | REF | REF | DCN_chr12_91135484_91187817 | DCN | chr12 | 91135484 | 91187817 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:91146221 | A | G | 1 | a0003 | 3 | HG02976.hp2 HG03130.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.917T>C | p.Val306Ala | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 1113/6850 | 917/1080 | 306/359 | chr12 | 91146221 | |||
| chr12:91151736 | G | A | 1 | a0002 | 9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
missense_variant | MODERATE | c.803C>T | p.Thr268Met | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/8 | 999/6850 | 803/1080 | 268/359 | chr12 | 91151736 | |||
| chr12:91158410 | T | C | 1 | a0004 | 2 | HG01123.hp1 HG01934.hp1 |
missense_variant | MODERATE | c.424A>G | p.Lys142Glu | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 4/8 | 620/6850 | 424/1080 | 142/359 | chr12 | 91158410 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:91146163 | C | T | 1 | a0001c0007 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.975G>A | p.Ser325Ser | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 1171/6850 | 975/1080 | 325/359 | chr12 | 91146163 | |||
| chr12:91153139 | T | G | 1 | a0001c0003 | 4 | HG01192.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
synonymous_variant | LOW | c.703A>C | p.Arg235Arg | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 6/8 | 899/6850 | 703/1080 | 235/359 | chr12 | 91153139 | |||
| chr12:91164647 | G | A | 2 | a0002c0002 a0002c0006 |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
synonymous_variant | LOW | c.282C>T | p.Thr94Thr | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/8 | 478/6850 | 282/1080 | 94/359 | chr12 | 91164647 | |||
| chr12:91178499 | C | T | 1 | a0002c0006 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.54G>A | p.Pro18Pro | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/8 | 250/6850 | 54/1080 | 18/359 | chr12 | 91178499 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:91140498 | T | C | 1 | a0001c0001t0009 | 3 | HG02630.hp1 HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5560A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 5560 | chr12 | 91140498 | ||||||
| chr12:91140653 | G | A | 1 | a0001c0001t0004 | 10 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5405C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 5405 | chr12 | 91140653 | ||||||
| chr12:91140727 | G | T | 1 | a0001c0001t0031 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5331C>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 5331 | chr12 | 91140727 | ||||||
| chr12:91140885 | A | G | 1 | a0001c0001t0007 | 4 | HG03041.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5173T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 5173 | chr12 | 91140885 | ||||||
| chr12:91141033 | C | T | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0018 others(1): Show |
28 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*5025G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 5025 | chr12 | 91141033 | ||||||
| chr12:91141107 | G | T | 1 | a0001c0001t0007 | 4 | HG03041.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4951C>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 4951 | chr12 | 91141107 | ||||||
| chr12:91141199 | C | T | 1 | a0001c0001t0024 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4859G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 4859 | chr12 | 91141199 | ||||||
| chr12:91141312 | G | T | 1 | a0001c0001t0015 | 2 | HG02895.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4746C>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 4746 | chr12 | 91141312 | ||||||
| chr12:91141363 | C | T | 1 | a0001c0001t0011 | 3 | HG02145.hp1 HG02451.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4695G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 4695 | chr12 | 91141363 | ||||||
| chr12:91141452 | C | T | 1 | a0001c0001t0014 | 2 | HG00733.hp2 HG01243.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4606G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 4606 | chr12 | 91141452 | ||||||
| chr12:91141528 | G | A | 1 | a0001c0001t0010 | 3 | HG01255.hp2 HG01358.hp1 HG02165.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4530C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 4530 | chr12 | 91141528 | ||||||
| chr12:91141563 | C | T | 1 | a0001c0001t0013 | 2 | NA18965.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4495G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 4495 | chr12 | 91141563 | ||||||
| chr12:91141626 | C | A | 1 | a0001c0001t0004 | 10 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4432G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 4432 | chr12 | 91141626 | ||||||
| chr12:91141628 | G | A | 1 | a0001c0003t0021 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4430C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 4430 | chr12 | 91141628 | ||||||
| chr12:91141664 | G | A | 1 | a0001c0001t0018 | 2 | HG02258.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4394C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 4394 | chr12 | 91141664 | ||||||
| chr12:91141981 | G | C | 1 | a0001c0001t0025 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4077C>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 4077 | chr12 | 91141981 | ||||||
| chr12:91142157 | A | G | 1 | a0001c0001t0006 | 8 | HG02273.hp1 NA18968.hp1 NA18970.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3901T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 3901 | chr12 | 91142157 | ||||||
| chr12:91142232 | T | A | 1 | a0001c0001t0026 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3826A>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 3826 | chr12 | 91142232 | ||||||
| chr12:91142395 | G | A | 1 | a0001c0001t0027 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3663C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 3663 | chr12 | 91142395 | ||||||
| chr12:91142485 | G | T | 1 | a0001c0001t0012 | 2 | HG02129.hp1 HG02165.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3573C>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 3573 | chr12 | 91142485 | ||||||
| chr12:91142493 | A | T | 1 | a0001c0001t0011 | 3 | HG02145.hp1 HG02451.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3565T>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 3565 | chr12 | 91142493 | ||||||
| chr12:91142561 | C | T | 2 | a0001c0003t0008 a0001c0003t0021 |
4 | HG01192.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3497G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 3497 | chr12 | 91142561 | ||||||
| chr12:91142637 | A | T | 2 | a0002c0002t0005 a0002c0006t0005 |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3421T>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 3421 | chr12 | 91142637 | ||||||
| chr12:91143152 | T | C | 1 | a0001c0001t0028 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2906A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 2906 | chr12 | 91143152 | ||||||
| chr12:91143254 | A | G | 3 | a0001c0001t0004 a0001c0003t0008 a0001c0003t0021 |
14 | HG01167.hp1 HG01192.hp2 HG02109.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2804T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 2804 | chr12 | 91143254 | ||||||
| chr12:91143565 | T | G | 1 | a0001c0001t0030 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2493A>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 2493 | chr12 | 91143565 | ||||||
| chr12:91143597 | A | G | 2 | a0001c0001t0003 a0001c0001t0020 |
13 | HG02055.hp1 HG02257.hp1 HG02647.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2461T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 2461 | chr12 | 91143597 | ||||||
| chr12:91143682 | G | GA | 2 | a0002c0002t0005 a0002c0006t0005 |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2375dupT | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 2375 | chr12 | 91143682 | ||||||
| chr12:91143687 | G | C | 1 | a0001c0001t0007 | 4 | HG03041.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2371C>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 2371 | chr12 | 91143687 | ||||||
| chr12:91143856 | G | GTA | 1 | a0001c0001t0016 | 2 | HG01256.hp1 HG02735.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2200_*2201dupTA | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 2201 | chr12 | 91143856 | ||||||
| chr12:91143870 | A | T | 1 | a0001c0001t0023 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2188T>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 2188 | chr12 | 91143870 | ||||||
| chr12:91144681 | A | G | 2 | a0001c0001t0003 a0001c0001t0020 |
13 | HG02055.hp1 HG02257.hp1 HG02647.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1377T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 1377 | chr12 | 91144681 | ||||||
| chr12:91144818 | T | G | 1 | a0001c0001t0029 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1240A>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 1240 | chr12 | 91144818 | ||||||
| chr12:91145138 | A | G | 1 | a0001c0001t0022 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*920T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 920 | chr12 | 91145138 | ||||||
| chr12:91145217 | C | T | 3 | a0001c0001t0004 a0001c0003t0008 a0001c0003t0021 |
14 | HG01167.hp1 HG01192.hp2 HG02109.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*841G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 841 | chr12 | 91145217 | ||||||
| chr12:91145710 | A | C | 1 | a0001c0001t0020 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*348T>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 348 | chr12 | 91145710 | ||||||
| chr12:91145738 | G | A | 1 | a0001c0001t0017 | 2 | HG02451.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*320C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 320 | chr12 | 91145738 | ||||||
| chr12:91145898 | G | A | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0018 others(1): Show |
28 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*160C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 160 | chr12 | 91145898 | ||||||
| chr12:91146007 | T | C | 2 | a0001c0001t0031 a0004c0005t0019 |
3 | HG01123.hp1 HG01934.hp1 HG02602.hp1 |
3_prime_UTR_variant | MODIFIER | c.*51A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 8/8 | 51 | chr12 | 91146007 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:91146326 | T | A | 1 | a0001c0001t0001g0136 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.886-74A>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91146326 | |||||||
| chr12:91146326 | T | C | 24 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(21): Show |
27 | HG01167.hp1 HG01192.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.886-74A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91146326 | |||||||
| chr12:91146351 | CT | C | 36 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0086 others(33): Show |
41 | HG00639.hp1 HG01167.hp1 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.886-100delA | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91146351 | |||||||
| chr12:91146517 | G | A | 1 | a0001c0001t0006g0037 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.886-265C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91146517 | |||||||
| chr12:91146655 | C | A | 2 | a0001c0001t0007g0018 a0001c0001t0007g0201 |
3 | HG03041.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.886-403G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91146655 | |||||||
| chr12:91146770 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.886-518T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91146770 | |||||||
| chr12:91147133 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.886-881T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91147133 | |||||||
| chr12:91147161 | T | C | 10 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(7): Show |
10 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.886-909A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91147161 | |||||||
| chr12:91147169 | C | A | 7 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(4): Show |
7 | HG01167.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.886-917G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91147169 | |||||||
| chr12:91147517 | C | T | 1 | a0001c0001t0010g0111 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.886-1265G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91147517 | |||||||
| chr12:91147548 | T | TTCAACC | 3 | a0001c0001t0003g0078 a0001c0001t0003g0079 a0001c0001t0003g0080 |
3 | HG02647.hp2 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.886-1297_886-1296i others(8): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91147548 | |||||||
| chr12:91147610 | A | C | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.886-1358T>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91147610 | |||||||
| chr12:91147621 | T | C | 10 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(7): Show |
10 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.886-1369A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91147621 | |||||||
| chr12:91147731 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA18956.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.886-1479C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91147731 | |||||||
| chr12:91147818 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.886-1566G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91147818 | |||||||
| chr12:91147822 | A | G | 1 | a0001c0001t0002g0051 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.886-1570T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91147822 | |||||||
| chr12:91148025 | C | G | 2 | a0001c0001t0016g0081 a0001c0001t0016g0082 |
2 | HG01256.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.886-1773G>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148025 | |||||||
| chr12:91148025 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.886-1773G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148025 | |||||||
| chr12:91148073 | CTTT | C | 28 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0048 others(25): Show |
28 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.886-1824_886-1822d others(5): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148073 | |||||||
| chr12:91148089 | T | C | 2 | a0001c0003t0008g0004 a0001c0003t0021g0204 |
4 | HG01192.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.886-1837A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148089 | |||||||
| chr12:91148156 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.886-1904G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148156 | |||||||
| chr12:91148218 | C | G | 3 | a0001c0001t0007g0018 a0001c0001t0007g0201 a0001c0001t0007g0206 |
4 | HG03041.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.886-1966G>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148218 | |||||||
| chr12:91148717 | G | A | 28 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0048 others(25): Show |
28 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.886-2465C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148717 | |||||||
| chr12:91148721 | C | CA | 44 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(41): Show |
55 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.886-2470dupT | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148721 | |||||||
| chr12:91148721 | C | CAA | 29 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(26): Show |
32 | HG00438.hp2 HG01070.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.886-2471_886-2470d others(4): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148721 | |||||||
| chr12:91148721 | C | CAAA | 6 | a0001c0001t0001g0132 a0001c0001t0001g0169 a0001c0001t0001g0175 others(3): Show |
7 | HG01358.hp1 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.886-2472_886-2470d others(5): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148721 | |||||||
| chr12:91148721 | C | CAAAAAAA others(2): Show |
7 | a0001c0001t0001g0074 a0001c0001t0001g0112 a0001c0001t0002g0044 others(4): Show |
7 | HG00609.hp1 HG00639.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.886-2478_886-2470d others(11): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148721 | |||||||
| chr12:91148721 | C | CAAAAAAA others(3): Show |
11 | a0001c0001t0001g0073 a0001c0001t0002g0050 a0001c0001t0002g0051 others(8): Show |
11 | HG00642.hp2 HG01243.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.886-2479_886-2470d others(12): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148721 | |||||||
| chr12:91148721 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0001g0094 a0001c0001t0002g0053 a0001c0001t0002g0055 others(1): Show |
4 | HG01884.hp2 HG03453.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.886-2480_886-2470d others(13): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148721 | |||||||
| chr12:91148721 | C | CAAAAAAA others(5): Show |
4 | a0001c0001t0002g0056 a0001c0001t0002g0062 a0001c0001t0002g0067 others(1): Show |
4 | HG03017.hp2 HG03516.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.886-2481_886-2470d others(14): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148721 | |||||||
| chr12:91148721 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0002g0063 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.886-2482_886-2470d others(15): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148721 | |||||||
| chr12:91148721 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0002g0045 a0001c0001t0002g0064 |
2 | HG02074.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.886-2483_886-2470d others(16): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148721 | |||||||
| chr12:91148721 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0018g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.886-2486_886-2470d others(19): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148721 | |||||||
| chr12:91148721 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0018g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.886-2489_886-2470d others(22): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148721 | |||||||
| chr12:91148721 | CAA | C | 17 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(14): Show |
17 | HG01167.hp1 HG01433.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.886-2471_886-2470d others(4): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148721 | |||||||
| chr12:91148750 | T | A | 3 | a0001c0001t0001g0071 a0001c0001t0010g0107 a0001c0001t0010g0111 |
3 | HG01255.hp2 HG01358.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.886-2498A>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148750 | |||||||
| chr12:91148750 | T | C | 21 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(18): Show |
23 | HG01167.hp1 HG01192.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.886-2498A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148750 | |||||||
| chr12:91148755 | A | G | 2 | a0001c0003t0008g0004 a0001c0003t0021g0204 |
4 | HG01192.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.886-2503T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148755 | |||||||
| chr12:91148831 | C | A | 4 | a0001c0001t0006g0034 a0001c0001t0006g0036 a0001c0001t0006g0037 others(1): Show |
4 | HG02273.hp1 NA18970.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.886-2579G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148831 | |||||||
| chr12:91148868 | A | C | 1 | a0001c0001t0002g0064 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.886-2616T>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148868 | |||||||
| chr12:91148945 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.886-2693A>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148945 | |||||||
| chr12:91148947 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.886-2695G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91148947 | |||||||
| chr12:91149015 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.885+2639C>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91149015 | |||||||
| chr12:91149142 | G | GA | 23 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(20): Show |
26 | HG01167.hp1 HG01192.hp2 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.885+2511dupT | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91149142 | |||||||
| chr12:91149694 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.885+1960A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91149694 | |||||||
| chr12:91149809 | A | C | 2 | a0001c0001t0002g0048 a0001c0001t0002g0050 |
2 | HG00639.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.885+1845T>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91149809 | |||||||
| chr12:91149872 | G | A | 2 | a0001c0003t0008g0004 a0001c0003t0021g0204 |
4 | HG01192.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.885+1782C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91149872 | |||||||
| chr12:91149873 | C | A | 2 | a0001c0003t0008g0004 a0001c0003t0021g0204 |
4 | HG01192.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.885+1781G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91149873 | |||||||
| chr12:91149891 | A | G | 21 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(18): Show |
23 | HG01167.hp1 HG01192.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.885+1763T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91149891 | |||||||
| chr12:91150002 | A | G | 1 | a0001c0001t0007g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.885+1652T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91150002 | |||||||
| chr12:91150046 | T | C | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.885+1608A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91150046 | |||||||
| chr12:91150054 | T | G | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.885+1600A>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91150054 | |||||||
| chr12:91150250 | C | T | 5 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0001c0001t0002g0060 others(2): Show |
5 | NA18941.hp1 NA18953.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.885+1404G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91150250 | |||||||
| chr12:91150326 | G | A | 1 | a0001c0007t0001g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.885+1328C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91150326 | |||||||
| chr12:91150644 | G | A | 1 | a0001c0007t0001g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.885+1010C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91150644 | |||||||
| chr12:91150850 | A | C | 21 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(18): Show |
23 | HG01167.hp1 HG01192.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.885+804T>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91150850 | |||||||
| chr12:91150863 | A | G | 3 | a0001c0001t0007g0018 a0001c0001t0007g0201 a0001c0001t0007g0206 |
4 | HG03041.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.885+791T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91150863 | |||||||
| chr12:91151021 | C | T | 1 | a0001c0001t0004g0212 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.885+633G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91151021 | |||||||
| chr12:91151054 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.885+600C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91151054 | |||||||
| chr12:91151152 | C | T | 12 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(9): Show |
14 | HG01167.hp1 HG01192.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.885+502G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91151152 | |||||||
| chr12:91151189 | G | A | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.885+465C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91151189 | |||||||
| chr12:91151196 | A | AT | 12 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(9): Show |
14 | HG01167.hp1 HG01192.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.885+457dupA | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91151196 | |||||||
| chr12:91151196 | AT | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0073 a0001c0001t0001g0074 others(3): Show |
7 | HG00140.hp1 HG01261.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.885+457delA | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91151196 | |||||||
| chr12:91151233 | C | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0026 others(5): Show |
9 | HG00733.hp1 HG01993.hp1 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.885+421G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91151233 | |||||||
| chr12:91151261 | C | T | 3 | a0003c0004t0001g0021 a0003c0004t0001g0022 a0003c0004t0001g0157 |
3 | HG02976.hp2 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.885+393G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 7/7 | chr12 | 91151261 | |||||||
| chr12:91151875 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.747-83C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 6/7 | chr12 | 91151875 | |||||||
| chr12:91152218 | A | G | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.747-426T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 6/7 | chr12 | 91152218 | |||||||
| chr12:91152226 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0167 |
2 | NA18943.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.747-434G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 6/7 | chr12 | 91152226 | |||||||
| chr12:91152300 | C | CAT | 2 | a0001c0001t0002g0066 a0001c0001t0002g0070 |
2 | HG00642.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.747-510_747-509dup others(2): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 6/7 | chr12 | 91152300 | |||||||
| chr12:91152300 | C | CATAT | 2 | a0001c0001t0007g0018 a0001c0001t0007g0201 |
3 | HG03041.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.747-512_747-509dup others(4): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 6/7 | chr12 | 91152300 | |||||||
| chr12:91152300 | C | CATATATA others(5): Show |
1 | a0001c0001t0004g0213 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.747-520_747-509dup others(12): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 6/7 | chr12 | 91152300 | |||||||
| chr12:91152300 | C | CATATATA others(7): Show |
10 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(7): Show |
12 | HG01167.hp1 HG01192.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.747-522_747-509dup others(14): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 6/7 | chr12 | 91152300 | |||||||
| chr12:91152300 | C | CATATATA others(17): Show |
1 | a0001c0001t0004g0209 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.747-509_747-508ins others(24): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 6/7 | chr12 | 91152300 | |||||||
| chr12:91152300 | C | CATATATA others(23): Show |
1 | a0001c0001t0007g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.747-509_747-508ins others(30): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 6/7 | chr12 | 91152300 | |||||||
| chr12:91152314 | T | TATAAGAC others(12): Show |
9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.747-523_747-522ins others(19): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 6/7 | chr12 | 91152314 | |||||||
| chr12:91152415 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0035 |
2 | NA19076.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.747-623C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 6/7 | chr12 | 91152415 | |||||||
| chr12:91152674 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.746+422A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 6/7 | chr12 | 91152674 | |||||||
| chr12:91152736 | A | T | 8 | a0001c0001t0003g0006 a0001c0001t0003g0020 a0001c0001t0003g0087 others(5): Show |
9 | HG02055.hp1 HG02257.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.746+360T>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 6/7 | chr12 | 91152736 | |||||||
| chr12:91152813 | T | C | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.746+283A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 6/7 | chr12 | 91152813 | |||||||
| chr12:91152950 | T | C | 1 | a0001c0001t0007g0018 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.746+146A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 6/7 | chr12 | 91152950 | |||||||
| chr12:91153053 | C | T | 1 | a0001c0003t0021g0204 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.746+43G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 6/7 | chr12 | 91153053 | |||||||
| chr12:91153213 | T | C | 12 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(9): Show |
14 | HG01167.hp1 HG01192.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.653-24A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91153213 | |||||||
| chr12:91153253 | A | G | 24 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(21): Show |
27 | HG01167.hp1 HG01192.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.653-64T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91153253 | |||||||
| chr12:91153399 | T | C | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.653-210A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91153399 | |||||||
| chr12:91153456 | TAGA | T | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.653-270_653-268del others(3): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91153456 | |||||||
| chr12:91153474 | C | T | 2 | a0001c0001t0009g0159 a0001c0001t0009g0182 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.653-285G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91153474 | |||||||
| chr12:91153566 | C | T | 3 | a0001c0001t0007g0018 a0001c0001t0007g0201 a0001c0001t0007g0206 |
4 | HG03041.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.653-377G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91153566 | |||||||
| chr12:91153567 | G | A | 2 | a0001c0001t0012g0129 a0001c0001t0012g0164 |
2 | HG02129.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.653-378C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91153567 | |||||||
| chr12:91153588 | G | A | 1 | a0001c0007t0001g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.653-399C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91153588 | |||||||
| chr12:91153662 | A | G | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.653-473T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91153662 | |||||||
| chr12:91153906 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.653-717G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91153906 | |||||||
| chr12:91153919 | T | C | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.653-730A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91153919 | |||||||
| chr12:91154010 | C | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0152 |
2 | HG01891.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.653-821G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91154010 | |||||||
| chr12:91154201 | C | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0122 |
3 | NA18970.hp1 NA18994.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.653-1012G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91154201 | |||||||
| chr12:91154209 | G | T | 3 | a0001c0001t0007g0018 a0001c0001t0007g0201 a0001c0001t0007g0206 |
4 | HG03041.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.653-1020C>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91154209 | |||||||
| chr12:91154357 | C | T | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.653-1168G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91154357 | |||||||
| chr12:91154424 | A | G | 1 | a0001c0001t0002g0059 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.653-1235T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91154424 | |||||||
| chr12:91154435 | C | CAA | 53 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0048 others(50): Show |
56 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.653-1248_653-1247d others(4): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91154435 | |||||||
| chr12:91154440 | T | A | 53 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0048 others(50): Show |
56 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.653-1251A>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91154440 | |||||||
| chr12:91154596 | A | G | 1 | a0001c0001t0004g0207 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.653-1407T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91154596 | |||||||
| chr12:91154728 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.653-1539G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91154728 | |||||||
| chr12:91154737 | G | T | 1 | a0001c0001t0001g0025 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.653-1548C>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91154737 | |||||||
| chr12:91154874 | G | T | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.653-1685C>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91154874 | |||||||
| chr12:91155062 | C | T | 1 | a0001c0001t0003g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.653-1873G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91155062 | |||||||
| chr12:91155093 | G | A | 2 | a0001c0003t0008g0004 a0001c0003t0021g0204 |
4 | HG01192.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.653-1904C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91155093 | |||||||
| chr12:91155296 | C | T | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.652+1779G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91155296 | |||||||
| chr12:91155464 | G | A | 6 | a0001c0001t0002g0048 a0001c0001t0002g0050 a0001c0001t0002g0052 others(3): Show |
6 | HG00639.hp2 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.652+1611C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91155464 | |||||||
| chr12:91155585 | T | G | 1 | a0001c0001t0001g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.652+1490A>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91155585 | |||||||
| chr12:91155615 | G | GATCT | 36 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0086 others(33): Show |
37 | HG00140.hp1 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.652+1456_652+1459d others(6): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91155615 | |||||||
| chr12:91155615 | G | GATCTATC others(1): Show |
25 | a0001c0001t0001g0074 a0001c0001t0001g0150 a0001c0001t0001g0153 others(22): Show |
25 | HG00642.hp2 HG01167.hp1 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.652+1452_652+1459d others(10): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91155615 | |||||||
| chr12:91155615 | G | GATCTATC others(5): Show |
3 | a0001c0001t0002g0056 a0001c0001t0002g0064 a0001c0001t0004g0214 |
3 | HG02074.hp1 HG02572.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.652+1448_652+1459d others(14): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91155615 | |||||||
| chr12:91155615 | GATCT | G | 10 | a0001c0001t0001g0112 a0001c0001t0001g0131 a0001c0001t0001g0147 others(7): Show |
11 | HG00639.hp2 HG01167.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.652+1456_652+1459d others(6): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91155615 | |||||||
| chr12:91155615 | GATCTATC others(1): Show |
G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(30): Show |
36 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.652+1452_652+1459d others(10): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91155615 | |||||||
| chr12:91155615 | GATCTATC others(5): Show |
G | 1 | a0001c0001t0002g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.652+1448_652+1459d others(14): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91155615 | |||||||
| chr12:91155653 | T | A | 1 | a0001c0001t0001g0101 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.652+1422A>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91155653 | |||||||
| chr12:91155738 | A | C | 21 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(18): Show |
23 | HG01167.hp1 HG01192.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.652+1337T>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91155738 | |||||||
| chr12:91155783 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.652+1292C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91155783 | |||||||
| chr12:91156060 | C | T | 21 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(18): Show |
23 | HG01167.hp1 HG01192.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.652+1015G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91156060 | |||||||
| chr12:91156232 | T | C | 1 | a0001c0001t0006g0036 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.652+843A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91156232 | |||||||
| chr12:91156358 | A | G | 5 | a0001c0001t0001g0085 a0001c0001t0001g0113 a0001c0001t0001g0114 others(2): Show |
5 | NA18956.hp1 NA18965.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.652+717T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91156358 | |||||||
| chr12:91156401 | T | G | 3 | a0001c0001t0007g0018 a0001c0001t0007g0201 a0001c0001t0007g0206 |
4 | HG03041.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.652+674A>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91156401 | |||||||
| chr12:91156486 | T | C | 5 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0210 others(2): Show |
5 | HG01167.hp1 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.652+589A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91156486 | |||||||
| chr12:91156608 | A | C | 3 | a0001c0001t0001g0141 a0001c0001t0001g0151 a0001c0001t0014g0011 |
4 | HG00733.hp2 HG01243.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.652+467T>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91156608 | |||||||
| chr12:91156622 | GA | G | 26 | a0001c0001t0001g0086 a0001c0001t0001g0130 a0001c0001t0001g0131 others(23): Show |
27 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.652+452delT | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91156622 | |||||||
| chr12:91156676 | C | T | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.652+399G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91156676 | |||||||
| chr12:91156695 | C | CT | 47 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(44): Show |
54 | HG00733.hp1 HG01070.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.652+379dupA | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91156695 | |||||||
| chr12:91156695 | CT | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0073 a0001c0001t0001g0074 others(6): Show |
11 | HG00140.hp1 HG01261.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.652+379delA | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91156695 | |||||||
| chr12:91156866 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.652+209G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91156866 | |||||||
| chr12:91157007 | A | AT | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.652+67dupA | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91157007 | |||||||
| chr12:91157007 | AT | A | 6 | a0001c0001t0001g0124 a0001c0001t0007g0018 a0001c0001t0007g0201 others(3): Show |
7 | HG02559.hp2 HG03041.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.652+67delA | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91157007 | |||||||
| chr12:91157052 | T | C | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.652+23A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 5/7 | chr12 | 91157052 | |||||||
| chr12:91157371 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.539-183G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 4/7 | chr12 | 91157371 | |||||||
| chr12:91157445 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.539-257G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 4/7 | chr12 | 91157445 | |||||||
| chr12:91157519 | A | G | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.539-331T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 4/7 | chr12 | 91157519 | |||||||
| chr12:91157630 | G | GA | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.539-443dupT | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 4/7 | chr12 | 91157630 | |||||||
| chr12:91157633 | A | AT | 34 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(31): Show |
37 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.539-446dupA | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 4/7 | chr12 | 91157633 | |||||||
| chr12:91157764 | T | G | 3 | a0001c0001t0007g0018 a0001c0001t0007g0201 a0001c0001t0007g0206 |
4 | HG03041.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.538+532A>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 4/7 | chr12 | 91157764 | |||||||
| chr12:91157879 | C | T | 5 | a0001c0001t0002g0048 a0001c0001t0002g0050 a0001c0001t0011g0046 others(2): Show |
5 | HG00639.hp2 HG02145.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.538+417G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 4/7 | chr12 | 91157879 | |||||||
| chr12:91158073 | T | C | 1 | a0001c0007t0001g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.538+223A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 4/7 | chr12 | 91158073 | |||||||
| chr12:91158131 | G | A | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0109 |
3 | NA18949.hp1 NA18988.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.538+165C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 4/7 | chr12 | 91158131 | |||||||
| chr12:91158277 | G | T | 1 | a0001c0001t0020g0019 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.538+19C>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 4/7 | chr12 | 91158277 | |||||||
| chr12:91158533 | C | A | 1 | a0001c0001t0001g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.325-24G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91158533 | |||||||
| chr12:91158535 | C | T | 3 | a0001c0001t0007g0018 a0001c0001t0007g0201 a0001c0001t0007g0206 |
4 | HG03041.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.325-26G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91158535 | |||||||
| chr12:91158783 | G | A | 1 | a0001c0001t0009g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.325-274C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91158783 | |||||||
| chr12:91158921 | G | A | 1 | a0001c0001t0004g0212 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.325-412C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91158921 | |||||||
| chr12:91159023 | T | C | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-514A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91159023 | |||||||
| chr12:91159092 | C | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0073 a0001c0001t0001g0074 others(6): Show |
10 | HG00140.hp1 HG01261.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.325-583G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91159092 | |||||||
| chr12:91159171 | T | A | 2 | a0001c0001t0009g0159 a0001c0001t0009g0182 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.325-662A>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91159171 | |||||||
| chr12:91159244 | C | T | 28 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0048 others(25): Show |
28 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.325-735G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91159244 | |||||||
| chr12:91159245 | G | T | 1 | a0002c0002t0005g0195 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.325-736C>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91159245 | |||||||
| chr12:91159306 | C | T | 3 | a0001c0001t0001g0141 a0001c0001t0001g0151 a0001c0001t0014g0011 |
4 | HG00733.hp2 HG01243.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.325-797G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91159306 | |||||||
| chr12:91159307 | G | A | 2 | a0002c0002t0005g0197 a0002c0006t0005g0192 |
2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.325-798C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91159307 | |||||||
| chr12:91159324 | G | T | 11 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0083 others(8): Show |
13 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.325-815C>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91159324 | |||||||
| chr12:91159378 | C | T | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-869G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91159378 | |||||||
| chr12:91159418 | AT | A | 17 | a0001c0001t0001g0017 a0001c0001t0001g0073 a0001c0001t0001g0074 others(14): Show |
18 | HG00140.hp1 HG01167.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.325-910delA | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91159418 | |||||||
| chr12:91159489 | T | C | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-980A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91159489 | |||||||
| chr12:91159712 | A | G | 8 | a0001c0001t0003g0006 a0001c0001t0003g0020 a0001c0001t0003g0087 others(5): Show |
9 | HG02055.hp1 HG02257.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-1203T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91159712 | |||||||
| chr12:91159801 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0180 |
2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.325-1292A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91159801 | |||||||
| chr12:91159925 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0110 |
3 | HG02040.hp2 HG02074.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.325-1416T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91159925 | |||||||
| chr12:91160177 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0115 |
2 | NA18965.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.325-1668G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91160177 | |||||||
| chr12:91160393 | C | T | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-1884G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91160393 | |||||||
| chr12:91160766 | A | T | 4 | a0001c0001t0002g0051 a0001c0001t0002g0055 a0001c0001t0002g0056 others(1): Show |
4 | HG01243.hp2 HG02647.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.325-2257T>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91160766 | |||||||
| chr12:91160808 | G | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0151 a0001c0001t0014g0011 |
4 | HG00733.hp2 HG01243.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.325-2299C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91160808 | |||||||
| chr12:91160950 | A | G | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-2441T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91160950 | |||||||
| chr12:91160951 | T | C | 1 | a0001c0001t0012g0129 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.325-2442A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91160951 | |||||||
| chr12:91160963 | ATTCT | A | 2 | a0001c0001t0010g0107 a0001c0001t0010g0111 |
2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.325-2458_325-2455d others(6): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91160963 | |||||||
| chr12:91161046 | T | A | 1 | a0001c0001t0001g0154 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.325-2537A>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91161046 | |||||||
| chr12:91161069 | A | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA18956.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.325-2560T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91161069 | |||||||
| chr12:91161320 | T | A | 10 | a0001c0001t0007g0206 a0002c0002t0005g0193 a0002c0002t0005g0194 others(7): Show |
10 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.325-2811A>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91161320 | |||||||
| chr12:91161389 | A | G | 5 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0001c0001t0002g0060 others(2): Show |
5 | NA18941.hp1 NA18953.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-2880T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91161389 | |||||||
| chr12:91161389 | A | T | 1 | a0001c0001t0001g0180 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.325-2880T>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91161389 | |||||||
| chr12:91161688 | C | A | 1 | a0001c0001t0016g0082 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.324+2917G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91161688 | |||||||
| chr12:91161769 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.324+2836G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91161769 | |||||||
| chr12:91161943 | A | AT | 57 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(54): Show |
61 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.324+2661dupA | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91161943 | |||||||
| chr12:91161943 | A | ATT | 9 | a0001c0001t0001g0096 a0002c0002t0005g0193 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+2660_324+2661d others(4): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91161943 | |||||||
| chr12:91161943 | AT | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0119 a0001c0001t0002g0066 others(2): Show |
5 | HG00642.hp2 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+2661delA | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91161943 | |||||||
| chr12:91161980 | A | G | 24 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(21): Show |
27 | HG01167.hp1 HG01192.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.324+2625T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91161980 | |||||||
| chr12:91162151 | G | T | 2 | a0001c0001t0007g0018 a0001c0001t0007g0201 |
3 | HG03041.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.324+2454C>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91162151 | |||||||
| chr12:91162301 | C | T | 1 | a0001c0001t0002g0063 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.324+2304G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91162301 | |||||||
| chr12:91162368 | T | G | 1 | a0001c0001t0001g0154 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.324+2237A>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91162368 | |||||||
| chr12:91162419 | T | C | 5 | a0001c0001t0001g0085 a0001c0001t0001g0113 a0001c0001t0001g0114 others(2): Show |
5 | NA18956.hp1 NA18965.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.324+2186A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91162419 | |||||||
| chr12:91162537 | T | C | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+2068A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91162537 | |||||||
| chr12:91162618 | A | G | 1 | a0001c0001t0007g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.324+1987T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91162618 | |||||||
| chr12:91162766 | G | C | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+1839C>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91162766 | |||||||
| chr12:91162780 | C | T | 1 | a0001c0001t0006g0041 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.324+1825G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91162780 | |||||||
| chr12:91162803 | G | A | 1 | a0001c0001t0024g0181 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.324+1802C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91162803 | |||||||
| chr12:91162868 | C | A | 1 | a0001c0001t0001g0146 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.324+1737G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91162868 | |||||||
| chr12:91162907 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.324+1698C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91162907 | |||||||
| chr12:91162928 | C | A | 1 | a0001c0001t0016g0081 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.324+1677G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91162928 | |||||||
| chr12:91162951 | A | G | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0180 others(1): Show |
4 | NA18522.hp1 NA18522.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+1654T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91162951 | |||||||
| chr12:91162953 | C | G | 2 | a0001c0003t0008g0004 a0001c0003t0021g0204 |
4 | HG01192.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+1652G>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91162953 | |||||||
| chr12:91162962 | G | C | 1 | a0001c0001t0001g0167 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.324+1643C>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91162962 | |||||||
| chr12:91163125 | C | T | 2 | a0001c0001t0007g0018 a0001c0001t0007g0201 |
3 | HG03041.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.324+1480G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91163125 | |||||||
| chr12:91163286 | A | G | 2 | a0001c0003t0008g0004 a0001c0003t0021g0204 |
4 | HG01192.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+1319T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91163286 | |||||||
| chr12:91163299 | A | G | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+1306T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91163299 | |||||||
| chr12:91163360 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.324+1245G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91163360 | |||||||
| chr12:91163492 | T | G | 12 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(9): Show |
14 | HG01167.hp1 HG01192.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.324+1113A>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91163492 | |||||||
| chr12:91163515 | T | C | 130 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(127): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.324+1090A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91163515 | |||||||
| chr12:91163542 | C | A | 1 | a0001c0001t0001g0147 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.324+1063G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91163542 | |||||||
| chr12:91163979 | A | T | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+626T>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91163979 | |||||||
| chr12:91164366 | T | TA | 84 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
89 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.324+238dupT | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91164366 | |||||||
| chr12:91164366 | T | TAA | 12 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(9): Show |
14 | HG01167.hp1 HG01192.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.324+237_324+238dup others(2): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91164366 | |||||||
| chr12:91164366 | TA | T | 11 | a0001c0001t0007g0018 a0001c0001t0007g0201 a0002c0002t0005g0193 others(8): Show |
12 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.324+238delT | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91164366 | |||||||
| chr12:91164400 | CA | C | 94 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(91): Show |
99 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.324+204delT | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91164400 | |||||||
| chr12:91164400 | CAA | C | 31 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(28): Show |
33 | HG00733.hp1 HG01993.hp1 HG02040.hp1 others(30): Show |
intron_variant | MODIFIER | c.324+203_324+204del others(2): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91164400 | |||||||
| chr12:91164400 | CAAAA | C | 13 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(10): Show |
15 | HG01167.hp1 HG01192.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.324+201_324+204del others(4): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91164400 | |||||||
| chr12:91164400 | CAAAAAAA | C | 26 | a0001c0001t0001g0086 a0001c0001t0001g0130 a0001c0001t0001g0131 others(23): Show |
27 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.324+198_324+204del others(7): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91164400 | |||||||
| chr12:91164452 | A | T | 1 | a0001c0007t0001g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.324+153T>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91164452 | |||||||
| chr12:91164462 | T | TA | 107 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(104): Show |
113 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.324+142dupT | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91164462 | |||||||
| chr12:91164462 | T | TAA | 19 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0025 others(16): Show |
20 | HG00733.hp1 HG01993.hp1 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.324+141_324+142dup others(2): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91164462 | |||||||
| chr12:91164462 | TA | T | 6 | a0001c0001t0001g0158 a0001c0001t0001g0176 a0001c0001t0001g0180 others(3): Show |
8 | HG01192.hp2 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.324+142delT | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91164462 | |||||||
| chr12:91164490 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.324+115A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91164490 | |||||||
| chr12:91164541 | G | C | 1 | a0001c0001t0001g0117 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.324+64C>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91164541 | |||||||
| chr12:91164587 | A | T | 1 | a0001c0001t0001g0176 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.324+18T>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 3/7 | chr12 | 91164587 | |||||||
| chr12:91164817 | A | G | 1 | a0002c0006t0005g0192 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.212-100T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91164817 | |||||||
| chr12:91164842 | C | A | 1 | a0001c0001t0012g0129 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.212-125G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91164842 | |||||||
| chr12:91164890 | T | G | 2 | a0001c0001t0007g0018 a0001c0001t0007g0201 |
3 | HG03041.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.212-173A>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91164890 | |||||||
| chr12:91165131 | C | A | 2 | a0001c0001t0007g0018 a0001c0001t0007g0201 |
3 | HG03041.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.212-414G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91165131 | |||||||
| chr12:91165258 | G | A | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-541C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91165258 | |||||||
| chr12:91165366 | A | G | 2 | a0001c0001t0004g0189 a0001c0001t0004g0190 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.212-649T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91165366 | |||||||
| chr12:91165420 | G | A | 130 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(127): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.212-703C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91165420 | |||||||
| chr12:91165669 | T | A | 1 | a0001c0001t0007g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.212-952A>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91165669 | |||||||
| chr12:91165751 | G | C | 1 | a0001c0001t0003g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.212-1034C>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91165751 | |||||||
| chr12:91165894 | C | T | 2 | a0001c0001t0007g0018 a0001c0001t0007g0201 |
3 | HG03041.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.212-1177G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91165894 | |||||||
| chr12:91166080 | G | A | 2 | a0001c0001t0002g0053 a0001c0001t0002g0054 |
2 | HG01884.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.212-1363C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91166080 | |||||||
| chr12:91166264 | G | A | 24 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(21): Show |
27 | HG01167.hp1 HG01192.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.212-1547C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91166264 | |||||||
| chr12:91166267 | A | C | 2 | a0001c0003t0008g0004 a0001c0003t0021g0204 |
4 | HG01192.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-1550T>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91166267 | |||||||
| chr12:91166352 | T | C | 35 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(32): Show |
38 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.212-1635A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91166352 | |||||||
| chr12:91166503 | T | A | 10 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(7): Show |
10 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-1786A>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91166503 | |||||||
| chr12:91166758 | A | T | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-2041T>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91166758 | |||||||
| chr12:91166859 | T | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0026 others(5): Show |
9 | HG00733.hp1 HG01993.hp1 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-2142A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91166859 | |||||||
| chr12:91166944 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0124 |
3 | HG01884.hp1 HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.212-2227A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91166944 | |||||||
| chr12:91166987 | C | A | 1 | a0001c0001t0007g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.212-2270G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91166987 | |||||||
| chr12:91167005 | A | G | 2 | a0001c0003t0008g0004 a0001c0003t0021g0204 |
4 | HG01192.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-2288T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91167005 | |||||||
| chr12:91167123 | T | A | 1 | a0001c0001t0002g0056 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.212-2406A>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91167123 | |||||||
| chr12:91167388 | C | T | 22 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(19): Show |
24 | HG01167.hp1 HG01192.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.212-2671G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91167388 | |||||||
| chr12:91167398 | T | TA | 34 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(31): Show |
38 | HG00733.hp1 HG01070.hp2 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.212-2682dupT | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91167398 | |||||||
| chr12:91167472 | G | GAC | 44 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0001g0150 others(41): Show |
45 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.212-2757_212-2756d others(4): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91167472 | |||||||
| chr12:91167472 | G | GACAC | 5 | a0001c0001t0002g0044 a0001c0001t0002g0054 a0001c0001t0002g0057 others(2): Show |
6 | HG01070.hp1 HG01243.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-2759_212-2756d others(6): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91167472 | |||||||
| chr12:91167472 | GAC | G | 11 | a0001c0001t0001g0096 a0001c0001t0001g0126 a0002c0002t0005g0193 others(8): Show |
11 | HG00438.hp2 HG01433.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.212-2757_212-2756d others(4): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91167472 | |||||||
| chr12:91167736 | A | G | 2 | a0001c0001t0007g0018 a0001c0001t0007g0201 |
3 | HG03041.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.212-3019T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91167736 | |||||||
| chr12:91167817 | C | T | 1 | a0001c0001t0007g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.212-3100G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91167817 | |||||||
| chr12:91168035 | G | T | 2 | a0001c0001t0002g0048 a0001c0001t0002g0050 |
2 | HG00639.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.212-3318C>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91168035 | |||||||
| chr12:91168044 | G | T | 1 | a0001c0001t0001g0029 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.212-3327C>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91168044 | |||||||
| chr12:91168080 | C | T | 1 | a0002c0002t0005g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.212-3363G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91168080 | |||||||
| chr12:91168130 | C | T | 1 | a0001c0003t0008g0004 | 3 | HG02258.hp2 HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.212-3413G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91168130 | |||||||
| chr12:91168270 | T | C | 10 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(7): Show |
10 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-3553A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91168270 | |||||||
| chr12:91168316 | G | C | 10 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(7): Show |
10 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-3599C>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91168316 | |||||||
| chr12:91168710 | T | A | 2 | a0001c0001t0007g0018 a0001c0001t0007g0201 |
3 | HG03041.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.212-3993A>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91168710 | |||||||
| chr12:91168860 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.212-4143T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91168860 | |||||||
| chr12:91168895 | T | C | 21 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(18): Show |
22 | HG00733.hp1 HG01993.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.212-4178A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91168895 | |||||||
| chr12:91168998 | T | C | 2 | a0001c0001t0007g0018 a0001c0001t0007g0201 |
3 | HG03041.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.212-4281A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91168998 | |||||||
| chr12:91169022 | CAATT | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(53): Show |
64 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.212-4309_212-4306d others(6): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91169022 | |||||||
| chr12:91169341 | A | T | 2 | a0001c0001t0002g0053 a0001c0001t0002g0054 |
2 | HG01884.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.212-4624T>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91169341 | |||||||
| chr12:91169378 | C | CA | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(4): Show |
7 | HG01346.hp1 HG01358.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.212-4662dupT | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91169378 | |||||||
| chr12:91169378 | C | CAA | 5 | a0002c0002t0005g0193 a0002c0002t0005g0198 a0002c0002t0005g0199 others(2): Show |
5 | HG01433.hp2 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-4663_212-4662d others(4): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91169378 | |||||||
| chr12:91169378 | C | CT | 2 | a0001c0001t0007g0206 a0001c0003t0008g0004 |
4 | HG02258.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-4662_212-4661i others(3): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91169378 | |||||||
| chr12:91169378 | C | CTA | 2 | a0001c0001t0012g0129 a0001c0003t0021g0204 |
2 | HG01192.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.212-4662_212-4661i others(4): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91169378 | |||||||
| chr12:91169378 | C | CTAAA | 12 | a0001c0001t0001g0025 a0001c0001t0001g0119 a0001c0001t0004g0189 others(9): Show |
12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.212-4662_212-4661i others(6): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91169378 | |||||||
| chr12:91169378 | C | CTAAAA | 42 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0024 others(39): Show |
43 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.212-4662_212-4661i others(7): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91169378 | |||||||
| chr12:91169378 | C | CTAAAAA | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(48): Show |
56 | HG00140.hp2 HG00408.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.212-4662_212-4661i others(8): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91169378 | |||||||
| chr12:91169378 | C | CTAAAAAA | 48 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(45): Show |
55 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.212-4662_212-4661i others(9): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91169378 | |||||||
| chr12:91169378 | C | CTAAAAAA others(1): Show |
17 | a0001c0001t0001g0009 a0001c0001t0001g0083 a0001c0001t0001g0084 others(14): Show |
18 | HG00408.hp1 HG01123.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.212-4662_212-4661i others(10): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91169378 | |||||||
| chr12:91169378 | C | CTAAAAAA others(2): Show |
2 | a0001c0001t0001g0085 a0001c0001t0001g0118 |
2 | NA18965.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.212-4662_212-4661i others(11): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91169378 | |||||||
| chr12:91169387 | A | T | 2 | a0001c0001t0007g0018 a0001c0001t0007g0201 |
3 | HG03041.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.212-4670T>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91169387 | |||||||
| chr12:91169402 | C | A | 2 | a0001c0001t0017g0185 a0001c0001t0017g0186 |
2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.212-4685G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91169402 | |||||||
| chr12:91169424 | A | T | 1 | a0001c0001t0001g0012 | 2 | HG01070.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.212-4707T>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91169424 | |||||||
| chr12:91169801 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.212-5084G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91169801 | |||||||
| chr12:91169926 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.212-5209A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91169926 | |||||||
| chr12:91170062 | TA | T | 14 | a0001c0001t0002g0058 a0001c0001t0004g0189 a0001c0001t0004g0190 others(11): Show |
16 | HG01167.hp1 HG01192.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.212-5346delT | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91170062 | |||||||
| chr12:91170079 | G | A | 1 | a0001c0001t0006g0041 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.212-5362C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91170079 | |||||||
| chr12:91170366 | A | G | 1 | a0001c0001t0015g0202 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.212-5649T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91170366 | |||||||
| chr12:91170499 | C | G | 2 | a0001c0003t0008g0004 a0001c0003t0021g0204 |
4 | HG01192.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-5782G>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91170499 | |||||||
| chr12:91170575 | C | G | 8 | a0001c0001t0003g0006 a0001c0001t0003g0020 a0001c0001t0003g0087 others(5): Show |
9 | HG02055.hp1 HG02257.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-5858G>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91170575 | |||||||
| chr12:91170594 | C | A | 1 | a0001c0001t0007g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.212-5877G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91170594 | |||||||
| chr12:91170704 | G | A | 10 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(7): Show |
10 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-5987C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91170704 | |||||||
| chr12:91170721 | G | A | 10 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(7): Show |
10 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-6004C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91170721 | |||||||
| chr12:91170775 | G | A | 2 | a0001c0001t0007g0018 a0001c0001t0007g0201 |
3 | HG03041.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.212-6058C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91170775 | |||||||
| chr12:91170777 | C | T | 1 | a0004c0005t0019g0127 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.212-6060G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91170777 | |||||||
| chr12:91170921 | A | G | 1 | a0002c0002t0005g0193 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.212-6204T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91170921 | |||||||
| chr12:91171142 | G | A | 130 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(127): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.212-6425C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91171142 | |||||||
| chr12:91171145 | C | T | 5 | a0001c0001t0002g0048 a0001c0001t0002g0050 a0001c0001t0011g0046 others(2): Show |
5 | HG00639.hp2 HG02145.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-6428G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91171145 | |||||||
| chr12:91171462 | G | T | 1 | a0004c0005t0019g0127 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.212-6745C>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91171462 | |||||||
| chr12:91171463 | C | T | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-6746G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91171463 | |||||||
| chr12:91171543 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.211+6799G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91171543 | |||||||
| chr12:91171566 | G | A | 21 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0207 others(18): Show |
22 | HG01167.hp1 HG01433.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.211+6776C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91171566 | |||||||
| chr12:91171694 | A | T | 1 | a0001c0001t0007g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.211+6648T>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91171694 | |||||||
| chr12:91171750 | T | G | 14 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0058 others(11): Show |
14 | HG00609.hp1 HG00642.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.211+6592A>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91171750 | |||||||
| chr12:91171917 | T | C | 52 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(49): Show |
55 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.211+6425A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91171917 | |||||||
| chr12:91171952 | C | CT | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.211+6389dupA | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91171952 | |||||||
| chr12:91172036 | G | T | 3 | a0003c0004t0001g0021 a0003c0004t0001g0022 a0003c0004t0001g0157 |
3 | HG02976.hp2 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.211+6306C>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91172036 | |||||||
| chr12:91172063 | A | T | 1 | a0001c0001t0007g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.211+6279T>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91172063 | |||||||
| chr12:91172106 | CA | C | 130 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(127): Show |
139 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.211+6235delT | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91172106 | |||||||
| chr12:91172149 | CT | C | 79 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(76): Show |
83 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.211+6192delA | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91172149 | |||||||
| chr12:91172259 | C | T | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.211+6083G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91172259 | |||||||
| chr12:91172311 | AT | A | 2 | a0001c0003t0008g0004 a0001c0003t0021g0204 |
4 | HG01192.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+6030delA | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91172311 | |||||||
| chr12:91172473 | C | T | 1 | a0001c0001t0002g0044 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.211+5869G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91172473 | |||||||
| chr12:91172536 | G | C | 1 | a0001c0001t0007g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.211+5806C>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91172536 | |||||||
| chr12:91172719 | T | G | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.211+5623A>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91172719 | |||||||
| chr12:91172794 | TAAAGAGT others(4): Show |
T | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.211+5537_211+5547d others(13): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91172794 | |||||||
| chr12:91172799 | A | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA18956.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.211+5543T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91172799 | |||||||
| chr12:91172875 | A | AAG | 10 | a0001c0001t0007g0206 a0002c0002t0005g0193 a0002c0002t0005g0194 others(7): Show |
10 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+5466_211+5467i others(4): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91172875 | |||||||
| chr12:91172984 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.211+5358T>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91172984 | |||||||
| chr12:91173013 | T | C | 1 | a0001c0001t0007g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.211+5329A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91173013 | |||||||
| chr12:91173146 | T | A | 1 | a0001c0001t0001g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.211+5196A>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91173146 | |||||||
| chr12:91173212 | C | A | 1 | a0001c0001t0001g0119 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.211+5130G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91173212 | |||||||
| chr12:91173291 | A | C | 1 | a0001c0001t0001g0089 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.211+5051T>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91173291 | |||||||
| chr12:91173405 | C | T | 1 | a0001c0001t0007g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.211+4937G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91173405 | |||||||
| chr12:91173828 | C | G | 1 | a0001c0001t0020g0019 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.211+4514G>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91173828 | |||||||
| chr12:91173984 | G | A | 28 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0048 others(25): Show |
28 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.211+4358C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91173984 | |||||||
| chr12:91174023 | C | T | 64 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(61): Show |
68 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.211+4319G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91174023 | |||||||
| chr12:91174097 | T | C | 2 | a0001c0003t0008g0004 a0001c0003t0021g0204 |
4 | HG01192.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+4245A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91174097 | |||||||
| chr12:91174130 | A | G | 73 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(70): Show |
77 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.211+4212T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91174130 | |||||||
| chr12:91174147 | T | A | 1 | a0001c0001t0002g0069 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.211+4195A>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91174147 | |||||||
| chr12:91174323 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.211+4019A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91174323 | |||||||
| chr12:91174335 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.211+4007T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91174335 | |||||||
| chr12:91174341 | C | G | 2 | a0001c0001t0018g0042 a0001c0001t0018g0043 |
2 | HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.211+4001G>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91174341 | |||||||
| chr12:91174518 | A | T | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.211+3824T>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91174518 | |||||||
| chr12:91174723 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.211+3619C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91174723 | |||||||
| chr12:91175010 | A | G | 53 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(50): Show |
56 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.211+3332T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91175010 | |||||||
| chr12:91175109 | A | G | 1 | a0001c0001t0007g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.211+3233T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91175109 | |||||||
| chr12:91175249 | A | G | 1 | a0001c0001t0003g0087 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.211+3093T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91175249 | |||||||
| chr12:91175339 | TA | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(73): Show |
84 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.211+3002delT | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91175339 | |||||||
| chr12:91175930 | C | A | 1 | a0001c0001t0007g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.211+2412G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91175930 | |||||||
| chr12:91176020 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.211+2322C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91176020 | |||||||
| chr12:91176435 | T | G | 2 | a0001c0001t0007g0018 a0001c0001t0007g0201 |
3 | HG03041.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.211+1907A>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91176435 | |||||||
| chr12:91176556 | A | G | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.211+1786T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91176556 | |||||||
| chr12:91176558 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.211+1784T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91176558 | |||||||
| chr12:91176829 | C | T | 8 | a0001c0001t0004g0207 a0001c0001t0004g0208 a0001c0001t0004g0209 others(5): Show |
8 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.211+1513G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91176829 | |||||||
| chr12:91176939 | C | T | 1 | a0001c0001t0031g0125 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.211+1403G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91176939 | |||||||
| chr12:91177127 | T | C | 2 | a0001c0001t0007g0018 a0001c0001t0007g0201 |
3 | HG03041.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.211+1215A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91177127 | |||||||
| chr12:91177208 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.211+1134T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91177208 | |||||||
| chr12:91177309 | A | G | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.211+1033T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91177309 | |||||||
| chr12:91177373 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.211+969C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91177373 | |||||||
| chr12:91177482 | A | C | 2 | a0001c0001t0007g0018 a0001c0001t0007g0201 |
3 | HG03041.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.211+860T>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91177482 | |||||||
| chr12:91177925 | T | G | 3 | a0001c0001t0003g0078 a0001c0001t0003g0079 a0001c0001t0003g0080 |
3 | HG02647.hp2 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.211+417A>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91177925 | |||||||
| chr12:91178056 | TAGA | T | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.211+283_211+285del others(3): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91178056 | |||||||
| chr12:91178090 | A | T | 64 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(61): Show |
68 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.211+252T>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91178090 | |||||||
| chr12:91178278 | C | A | 1 | a0001c0001t0027g0121 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.211+64G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 2/7 | chr12 | 91178278 | |||||||
| chr12:91178627 | A | C | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-33-42T>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91178627 | |||||||
| chr12:91178638 | C | T | 62 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(59): Show |
65 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.-33-53G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91178638 | |||||||
| chr12:91178759 | G | A | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-33-174C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91178759 | |||||||
| chr12:91178957 | G | A | 62 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(59): Show |
65 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.-33-372C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91178957 | |||||||
| chr12:91179123 | T | C | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-33-538A>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91179123 | |||||||
| chr12:91179286 | C | G | 53 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(50): Show |
56 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.-33-701G>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91179286 | |||||||
| chr12:91179502 | C | T | 1 | a0001c0001t0028g0123 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-33-917G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91179502 | |||||||
| chr12:91179539 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-33-954G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91179539 | |||||||
| chr12:91179589 | T | A | 1 | a0001c0001t0007g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-33-1004A>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91179589 | |||||||
| chr12:91179655 | A | G | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-33-1070T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91179655 | |||||||
| chr12:91180000 | T | A | 1 | a0001c0001t0001g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-33-1415A>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180000 | |||||||
| chr12:91180049 | A | T | 4 | a0001c0001t0003g0077 a0001c0001t0003g0078 a0001c0001t0003g0079 others(1): Show |
4 | HG02647.hp2 HG03098.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33-1464T>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180049 | |||||||
| chr12:91180051 | G | GA | 64 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(61): Show |
68 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.-33-1467_-33-1466i others(3): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180051 | |||||||
| chr12:91180088 | G | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0122 |
3 | NA18970.hp1 NA18994.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-33-1503C>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180088 | |||||||
| chr12:91180113 | A | G | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-33-1528T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180113 | |||||||
| chr12:91180153 | C | T | 2 | a0001c0003t0008g0004 a0001c0003t0021g0204 |
4 | HG01192.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33-1568G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180153 | |||||||
| chr12:91180198 | CACTT | C | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-33-1617_-33-1614d others(6): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180198 | |||||||
| chr12:91180282 | T | TA | 64 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(61): Show |
68 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.-33-1698dupT | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180282 | |||||||
| chr12:91180299 | A | AAAG | 129 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(126): Show |
138 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.-33-1717_-33-1715d others(5): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180299 | |||||||
| chr12:91180310 | G | A | 1 | a0001c0001t0007g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-33-1725C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180310 | |||||||
| chr12:91180314 | A | G | 2 | a0001c0001t0007g0018 a0001c0001t0007g0201 |
3 | HG03041.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-33-1729T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180314 | |||||||
| chr12:91180329 | G | A | 64 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(61): Show |
68 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.-33-1744C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180329 | |||||||
| chr12:91180379 | T | TGAAAGAA others(1): Show |
54 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(51): Show |
58 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-33-1802_-33-1795d others(10): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180379 | |||||||
| chr12:91180386 | A | AAGAAAGA others(3): Show |
1 | a0001c0001t0001g0023 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-33-1802_-33-1801i others(12): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180386 | |||||||
| chr12:91180398 | G | A | 29 | a0001c0001t0001g0068 a0001c0001t0002g0044 a0001c0001t0002g0045 others(26): Show |
29 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.-33-1813C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180398 | |||||||
| chr12:91180402 | GAA | G | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-33-1819_-33-1818d others(4): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180402 | |||||||
| chr12:91180404 | A | G | 1 | a0001c0001t0007g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-33-1819T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180404 | |||||||
| chr12:91180489 | G | A | 1 | a0003c0004t0001g0022 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-33-1904C>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180489 | |||||||
| chr12:91180524 | G | C | 2 | a0001c0001t0007g0018 a0001c0001t0007g0201 |
3 | HG03041.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-33-1939C>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180524 | |||||||
| chr12:91180826 | A | G | 9 | a0002c0002t0005g0193 a0002c0002t0005g0194 a0002c0002t0005g0195 others(6): Show |
9 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34+1829T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180826 | |||||||
| chr12:91180886 | C | T | 17 | a0001c0001t0004g0207 a0001c0001t0004g0208 a0001c0001t0004g0209 others(14): Show |
17 | HG01167.hp1 HG01433.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-34+1769G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180886 | |||||||
| chr12:91180965 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
6 | HG00140.hp1 HG01261.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+1690T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91180965 | |||||||
| chr12:91181133 | CGT | C | 1 | a0001c0001t0001g0017 | 2 | HG01261.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-34+1520_-34+1521d others(4): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91181133 | |||||||
| chr12:91181149 | TGAGA | T | 55 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(52): Show |
59 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-34+1502_-34+1505d others(6): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91181149 | |||||||
| chr12:91181192 | CAGAG | C | 2 | a0001c0001t0007g0018 a0001c0001t0007g0201 |
3 | HG03041.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-34+1459_-34+1462d others(6): Show |
DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91181192 | |||||||
| chr12:91181377 | C | A | 64 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(61): Show |
68 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.-34+1278G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91181377 | |||||||
| chr12:91181430 | T | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(52): Show |
59 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-34+1225A>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91181430 | |||||||
| chr12:91181586 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-34+1069G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91181586 | |||||||
| chr12:91181656 | T | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(52): Show |
59 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-34+999A>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91181656 | |||||||
| chr12:91181671 | G | C | 55 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(52): Show |
59 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-34+984C>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91181671 | |||||||
| chr12:91181899 | C | A | 2 | a0001c0001t0004g0189 a0001c0001t0004g0190 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-34+756G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91181899 | |||||||
| chr12:91181902 | G | GA | 72 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(69): Show |
76 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.-34+752dupT | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91181902 | |||||||
| chr12:91181991 | C | A | 1 | a0001c0001t0007g0206 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-34+664G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91181991 | |||||||
| chr12:91182085 | T | G | 11 | a0001c0001t0007g0018 a0001c0001t0007g0201 a0002c0002t0005g0193 others(8): Show |
12 | HG01433.hp2 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-34+570A>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91182085 | |||||||
| chr12:91182093 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-34+562T>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91182093 | |||||||
| chr12:91182143 | C | G | 53 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(50): Show |
56 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.-34+512G>C | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91182143 | |||||||
| chr12:91182208 | C | A | 2 | a0001c0001t0015g0202 a0001c0001t0015g0203 |
2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-34+447G>T | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91182208 | |||||||
| chr12:91182332 | C | T | 2 | a0003c0004t0001g0021 a0003c0004t0001g0022 |
2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-34+323G>A | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91182332 | |||||||
| chr12:91182523 | A | C | 2 | a0001c0001t0003g0020 a0001c0001t0020g0019 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-34+132T>G | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91182523 | |||||||
| chr12:91182546 | GT | G | 12 | a0001c0001t0004g0207 a0001c0001t0004g0208 a0001c0001t0004g0209 others(9): Show |
14 | HG01167.hp1 HG01192.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-34+108delA | DCN | ENSG00000011465.18 | transcript | ENST00000052754.10 | protein_coding | 1/7 | chr12 | 91182546 |