Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 203447 |
|---|---|
| ensemblid | ENSG00000123572.17 |
| hgncid | 25391 |
| symbol | NRK |
| name | Nik related kinase |
| refseq_nuc | NM_198465.4 |
| refseq_prot | NP_940867.2 |
| ensembl_nuc | ENST00000243300.14 |
| ensembl_prot | ENSP00000434830.1 |
| mane_status | MANE Select |
| chr | chrX |
| start | 105822539 |
| end | 105958610 |
| strand | + |
| ver | v1.2 |
| region | chrX:105822539-105958610 |
| region5000 | chrX:105817539-105963610 |
| regionname0 | NRK_chrX_105822539_105958610 |
| regionname5000 | NRK_chrX_105817539_105963610 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1582 | 125 | 17 | 23 | 62 | 4 | 17 | 51 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0002 | 0/0 | 1582 | 51 | 16 | 12 | 14 | 0 | 9 | 6 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0003 | 0/0 | 1582 | 29 | 28 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0004 | 0/0 | 1582 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0005 | 0/0 | 1582 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0006 | 0/0 | 1582 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0007 | 0/0 | 1582 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0008 | 0/0 | 1006 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0009 | 0/0 | 1582 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0010 | 0/0 | 1582 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0011 | 0/0 | 1540 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 4749 | 122 | 15 | 23 | 61 | 4 | 17 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| c0002 | 0/0 | 4749 | 50 | 15 | 12 | 14 | 0 | 9 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| c0003 | 0/0 | 4749 | 28 | 27 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| c0004 | 0/0 | 4749 | 7 | 7 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| c0005 | 0/0 | 4749 | 2 | 2 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| c0006 | 0/0 | 4623 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| c0007 | 0/0 | 4749 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| c0008 | 0/0 | 4749 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| c0009 | 0/0 | 4749 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| c0010 | 0/0 | 4749 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| c0011 | 0/0 | 4749 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| c0012 | 0/0 | 4749 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| c0013 | 0/0 | 4750 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| c0014 | 0/0 | 4749 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| c0015 | 0/0 | 4749 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 3318 | 106 | 5 | 20 | 61 | 2 | 17 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| t0002 | 0/0 | 3318 | 41 | 8 | 11 | 12 | 1 | 9 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| t0003 | 0/0 | 3318 | 37 | 35 | 2 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| t0004 | 0/1 | 3318 | 18 | 12 | 4 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| t0005 | 0/0 | 3318 | 9 | 7 | 0 | 2 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| t0006 | 0/0 | 3318 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| t0007 | 0/0 | 3317 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| t0008 | 0/0 | 3317 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| t0009 | 0/0 | 3317 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| t0010 | 0/0 | 3316 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| t0011 | 0/0 | 3318 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| t0012 | 0/0 | 3318 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| t0013 | 0/0 | 3317 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0191 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0193 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4749 | 122 | 15 | 23 | 61 | 4 | 17 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0001c0005 | 0/0 | 4749 | 2 | 2 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0001c0012 | 0/0 | 4749 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0002c0002 | 0/0 | 4749 | 50 | 15 | 12 | 14 | 0 | 9 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0002c0009 | 0/0 | 4749 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0003c0003 | 0/0 | 4749 | 28 | 27 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0003c0011 | 0/0 | 4749 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0004c0004 | 0/0 | 4749 | 7 | 7 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0005c0007 | 0/0 | 4749 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0006c0008 | 0/0 | 4749 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0007c0010 | 0/0 | 4749 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0008c0013 | 0/0 | 4750 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0009c0014 | 0/0 | 4749 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0010c0015 | 0/0 | 4749 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0011c0006 | 0/0 | 4623 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 8066 | 100 | 3 | 18 | 59 | 2 | 17 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0001c0001t0004 | 0/1 | 8066 | 18 | 12 | 4 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0001c0001t0006 | 0/0 | 8066 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0001c0001t0007 | 0/0 | 8065 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0001c0001t0008 | 0/0 | 8065 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0001c0001t0009 | 0/0 | 8065 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0001c0005t0001 | 0/0 | 8066 | 2 | 2 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0001c0012t0001 | 0/0 | 8066 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0002c0002t0002 | 0/0 | 8066 | 40 | 8 | 11 | 12 | 0 | 9 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0002c0002t0005 | 0/0 | 8066 | 7 | 5 | 0 | 2 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0002c0002t0011 | 0/0 | 8066 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0002c0002t0012 | 0/0 | 8066 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0002c0002t0013 | 0/0 | 8065 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0002c0009t0005 | 0/0 | 8066 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0003c0003t0003 | 0/0 | 8066 | 28 | 27 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0003c0011t0003 | 0/0 | 8066 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0004c0004t0003 | 0/0 | 8066 | 7 | 7 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0005c0007t0003 | 0/0 | 8066 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0006c0008t0002 | 0/0 | 8066 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0007c0010t0005 | 0/0 | 8066 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0008c0013t0001 | 0/0 | 8067 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0009c0014t0001 | 0/0 | 8066 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0010c0015t0010 | 0/0 | 8064 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| a0011c0006t0001 | 0/0 | 7940 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | copy fasta | chrX | 105817539 | 105963610 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0191 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0193 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0007g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0008g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0009g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0005t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0012t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0011g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0012g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0013g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0009t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0011t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0004c0004t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0004c0004t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0004c0004t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0004c0004t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0004c0004t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0004c0004t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0004c0004t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0005c0007t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0006c0008t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0007c0010t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0008c0013t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0009c0014t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0010c0015t0010g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0011c0006t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0009 | g0192 | EUR | GBR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0194 | EUR | FIN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | CHS | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0057 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0049 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0206 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0077 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0050 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01074 | hp1 | a0009 | c0014 | t0001 | g0135 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01109 | hp1 | a0003 | c0003 | t0003 | g0023 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0086 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0196 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0085 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01169 | hp2 | a0002 | c0002 | t0013 | g0003 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0059 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01243 | hp1 | a0005 | c0007 | t0003 | g0017 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0052 | AMR | CLM | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0173 | AMR | CLM | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0190 | AMR | CLM | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0043 | AMR | CLM | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0055 | AMR | CLM | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01515 | hp1 | a0006 | c0008 | t0002 | g0042 | EUR | IBS | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0046 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01884 | hp2 | a0003 | c0003 | t0003 | g0038 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0197 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01891 | hp2 | a0004 | c0004 | t0003 | g0014 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01981 | hp1 | a0011 | c0006 | t0001 | g0117 | AMR | PEL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0048 | AMR | PEL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0065 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0105 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02145 | hp1 | a0004 | c0004 | t0003 | g0018 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02258 | hp1 | a0003 | c0003 | t0003 | g0007 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02451 | hp1 | a0003 | c0003 | t0003 | g0213 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02451 | hp2 | a0002 | c0002 | t0011 | g0201 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02572 | hp1 | a0003 | c0003 | t0003 | g0032 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0132 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02622 | hp2 | a0003 | c0011 | t0003 | g0037 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02630 | hp1 | a0003 | c0003 | t0003 | g0009 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02630 | hp2 | a0003 | c0003 | t0003 | g0030 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02647 | hp1 | a0001 | c0005 | t0001 | g0004 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0053 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02717 | hp1 | a0002 | c0002 | t0012 | g0103 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0187 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02723 | hp2 | a0003 | c0003 | t0003 | g0034 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0054 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02809 | hp1 | a0003 | c0003 | t0003 | g0031 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02809 | hp2 | a0002 | c0009 | t0005 | g0209 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0090 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02818 | hp2 | a0003 | c0003 | t0003 | g0008 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02886 | hp1 | a0003 | c0003 | t0003 | g0012 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0062 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02895 | hp1 | a0003 | c0003 | t0003 | g0040 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02897 | hp1 | a0003 | c0003 | t0003 | g0039 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02897 | hp2 | a0010 | c0015 | t0010 | g0176 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02922 | hp1 | a0004 | c0004 | t0003 | g0021 | AFR | ESN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02922 | hp2 | a0003 | c0003 | t0003 | g0013 | AFR | ESN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02965 | hp1 | a0003 | c0003 | t0003 | g0029 | AFR | ESN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02970 | hp1 | a0002 | c0002 | t0005 | g0211 | AFR | ESN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02970 | hp2 | a0004 | c0004 | t0003 | g0022 | AFR | ESN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02976 | hp1 | a0003 | c0003 | t0003 | g0027 | AFR | ESN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02976 | hp2 | a0007 | c0010 | t0005 | g0088 | AFR | ESN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0198 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0051 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03098 | hp1 | a0003 | c0003 | t0003 | g0026 | AFR | MSL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03130 | hp1 | a0002 | c0002 | t0005 | g0102 | AFR | ESN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | ESN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03209 | hp1 | a0003 | c0003 | t0003 | g0019 | AFR | MSL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03225 | hp1 | a0001 | c0005 | t0001 | g0004 | AFR | MSL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0058 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | MSL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03453 | hp2 | a0003 | c0003 | t0003 | g0011 | AFR | MSL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03486 | hp1 | a0004 | c0004 | t0003 | g0016 | AFR | MSL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03486 | hp2 | a0002 | c0002 | t0005 | g0208 | AFR | MSL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03540 | hp1 | a0004 | c0004 | t0003 | g0015 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0063 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03579 | hp1 | a0003 | c0003 | t0003 | g0212 | AFR | MSL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0045 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0047 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0072 | SAS | BEB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0064 | SAS | BEB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | STU | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0074 | SAS | BEB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | STU | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18522 | hp1 | a0003 | c0003 | t0003 | g0028 | AFR | YRI | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18612 | hp1 | a0002 | c0002 | t0005 | g0202 | EAS | CHB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0186 | AFR | YRI | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18906 | hp2 | a0003 | c0003 | t0003 | g0024 | AFR | YRI | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18961 | hp1 | a0002 | c0002 | t0005 | g0199 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18974 | hp1 | a0008 | c0013 | t0001 | g0041 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18984 | hp1 | a0001 | c0001 | t0008 | g0079 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0061 | AFR | LWK | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19043 | hp1 | a0002 | c0002 | t0005 | g0203 | AFR | LWK | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19058 | hp1 | a0001 | c0001 | t0007 | g0119 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19062 | hp1 | a0001 | c0012 | t0001 | g0089 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0205 | AFR | YRI | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19240 | hp2 | a0004 | c0004 | t0003 | g0020 | AFR | YRI | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0195 | AFR | ASW | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA20129 | hp2 | a0003 | c0003 | t0003 | g0036 | AFR | ASW | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | TSI | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | TSI | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0075 | SAS | GIH | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02109 | hp1 | a0002 | c0002 | t0005 | g0210 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02109 | hp2 | a0003 | c0003 | t0003 | g0006 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0060 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0092 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02559 | hp2 | a0003 | c0003 | t0003 | g0010 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0166 | AFR | MSL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG06807 | hp1 | a0003 | c0003 | t0003 | g0033 | AFR | USA | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0056 | AFR | USA | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | USA | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA20300 | hp2 | a0003 | c0003 | t0003 | g0025 | AFR | USA | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA21309 | hp1 | a0003 | c0003 | t0003 | g0035 | AFR | LWK | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | LWK | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0193 | REF | REF | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0191 | REF | REF | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:105887094
|
ATTAAAAT others(1388): Show |
A | 1 | a0011 | 1 | HG01981.hp1 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.253-1196_378+73del | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chrX | 105887094 | |||||
| chrX:105888396
|
C | T | 1 | a0010 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.355C>T | p.Pro119Ser | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/29 | 662/8066 | 355/4749 | 119/1582 | chrX | 105888396 | ||
| chrX:105908290
|
G | A | 7 | a0002a0003a0004others(4): Show | 91 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(88): Show |
missense_variant | MODERATE | c.1072G>A | p.Val358Met | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 12/29 | 1379/8066 | 1072/4749 | 358/1582 | chrX | 105908290 | ||
| chrX:105909821
|
G | A | 2 | a0004a0005 | 8 | HG01243.hp1 HG01891.hp2 HG02145.hp1 others(5): Show |
missense_variant | MODERATE | c.2180G>A | p.Arg727His | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/29 | 2487/8066 | 2180/4749 | 727/1582 | chrX | 105909821 | ||
| chrX:105915745
|
C | T | 1 | a0009 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.2365C>T | p.Pro789Ser | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/29 | 2672/8066 | 2365/4749 | 789/1582 | chrX | 105915745 | ||
| chrX:105923287
|
G | A | 1 | a0006 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.2780G>A | p.Ser927Asn | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/29 | 3087/8066 | 2780/4749 | 927/1582 | chrX | 105923287 | ||
| chrX:105924697
|
C | A | 3 | a0003a0004a0005 | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
missense_variant&splice_region_variant | MODERATE | c.2978C>A | p.Ala993Glu | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/29 | 3285/8066 | 2978/4749 | 993/1582 | chrX | 105924697 | ||
| chrX:105924719
|
C | CT | 1 | a0008 | 1 | NA18974.hp1 | frameshift_variant | HIGH | c.3001dupT | p.Cys1001fs | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/29 | 3309/8066 | 3002/4749 | 1001/1582 | INFO_REALIGN_3_PRIME | chrX | 105924719 | |
| chrX:105924827
|
C | A | 1 | a0007 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.3108C>A | p.Asp1036Glu | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/29 | 3415/8066 | 3108/4749 | 1036/1582 | chrX | 105924827 | ||
| chrX:105924862
|
C | G | 1 | a0005 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.3143C>G | p.Ala1048Gly | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/29 | 3450/8066 | 3143/4749 | 1048/1582 | chrX | 105924862 | ||
| chrX:105958608
|
A | T | 8 | a0001a0002a0003others(5): Show | 110 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(107): Show |
splice_region_variant | LOW | c.*3008A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | chrX | 105958608 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:105900620
|
T | C | 1 | a0001c0005 | 2 | HG02647.hp1 HG03225.hp1 |
splice_region_variant&synonymous_variant | LOW | c.714T>C | p.Ser238Ser | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/29 | 1021/8066 | 714/4749 | 238/1582 | chrX | 105900620 | ||
| chrX:105909048
|
A | G | 1 | a0003c0011 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1407A>G | p.Pro469Pro | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/29 | 1714/8066 | 1407/4749 | 469/1582 | chrX | 105909048 | ||
| chrX:105923468
|
G | A | 1 | a0002c0009 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.2961G>A | p.Ala987Ala | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/29 | 3268/8066 | 2961/4749 | 987/1582 | chrX | 105923468 | ||
| chrX:105939912
|
T | C | 1 | a0001c0012 | 1 | NA19062.hp1 | synonymous_variant | LOW | c.3838T>C | p.Leu1280Leu | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/29 | 4145/8066 | 3838/4749 | 1280/1582 | chrX | 105939912 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:105822592
|
T | G | 4 | a0003c0003t0003a0003c0011t0003a0004c0004t0003others(1): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
5_prime_UTR_variant | MODIFIER | c.-254T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/29 | 254 | chrX | 105822592 | |||||
| chrX:105955712
|
C | A | 1 | a0001c0001t0006 | 1 | HG01258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*112C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 112 | chrX | 105955712 | |||||
| chrX:105956698
|
G | T | 3 | a0002c0002t0002a0002c0002t0013a0006c0008t0002 | 42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1098G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1098 | chrX | 105956698 | |||||
| chrX:105956918
|
C | CG | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1318_*1319insG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1319 | chrX | 105956918 | |||||
| chrX:105956919
|
A | G | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1319A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1319 | chrX | 105956919 | |||||
| chrX:105956920
|
A | C | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1320A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1320 | chrX | 105956920 | |||||
| chrX:105956923
|
TATACC | T | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1324_*1328delATAC others(1): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1324 | chrX | 105956923 | |||||
| chrX:105956930
|
CAA | C | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1331_*1332delAA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1331 | chrX | 105956930 | |||||
| chrX:105956934
|
A | G | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1334A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1334 | chrX | 105956934 | |||||
| chrX:105956936
|
A | T | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1336A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1336 | chrX | 105956936 | |||||
| chrX:105956937
|
A | G | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1337A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1337 | chrX | 105956937 | |||||
| chrX:105956938
|
T | C | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1338T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1338 | chrX | 105956938 | |||||
| chrX:105956940
|
C | T | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1340C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1340 | chrX | 105956940 | |||||
| chrX:105956946
|
G | T | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1346G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1346 | chrX | 105956946 | |||||
| chrX:105956947
|
T | TGCC | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1347_*1348insGCC | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1348 | chrX | 105956947 | |||||
| chrX:105956948
|
T | C | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1348T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1348 | chrX | 105956948 | |||||
| chrX:105956950
|
T | A | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1350T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1350 | chrX | 105956950 | |||||
| chrX:105956952
|
C | A | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1352C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1352 | chrX | 105956952 | |||||
| chrX:105956953
|
T | A | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1353T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1353 | chrX | 105956953 | |||||
| chrX:105956955
|
C | T | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1355C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1355 | chrX | 105956955 | |||||
| chrX:105956958
|
A | C | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1358A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1358 | chrX | 105956958 | |||||
| chrX:105956959
|
A | C | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1359A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1359 | chrX | 105956959 | |||||
| chrX:105956961
|
T | TGGTA | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1361_*1362insGGTA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1362 | chrX | 105956961 | |||||
| chrX:105956962
|
C | T | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1362C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1362 | chrX | 105956962 | |||||
| chrX:105956969
|
C | T | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1369C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1369 | chrX | 105956969 | |||||
| chrX:105956970
|
A | G | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1370A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1370 | chrX | 105956970 | |||||
| chrX:105956971
|
G | GA | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1371_*1372insA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1372 | chrX | 105956971 | |||||
| chrX:105956974
|
CTAGTG | C | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1375_*1379delTAGT others(1): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1375 | chrX | 105956974 | |||||
| chrX:105956980
|
G | A | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1380G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1380 | chrX | 105956980 | |||||
| chrX:105956988
|
A | ATC | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1389_*1390insCT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1390 | INFO_REALIGN_3_PRIME | chrX | 105956988 | ||||
| chrX:105956990
|
T | C | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1390T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1390 | chrX | 105956990 | |||||
| chrX:105956995
|
A | T | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1395A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1395 | chrX | 105956995 | |||||
| chrX:105957010
|
C | CA | 1 | a0002c0002t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1414dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1415 | INFO_REALIGN_3_PRIME | chrX | 105957010 | ||||
| chrX:105957274
|
GT | G | 3 | a0001c0001t0008a0001c0001t0009a0002c0002t0013 | 3 | HG00140.hp1 HG01169.hp2 NA18984.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1686delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1686 | INFO_REALIGN_3_PRIME | chrX | 105957274 | ||||
| chrX:105957286
|
T | A | 1 | a0001c0001t0007 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1686T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1686 | chrX | 105957286 | |||||
| chrX:105957335
|
T | C | 1 | a0010c0015t0010 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1735T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1735 | chrX | 105957335 | |||||
| chrX:105957643
|
A | G | 13 | a0002c0002t0002a0002c0002t0005a0002c0002t0011others(10): Show | 91 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*2043A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 2043 | chrX | 105957643 | |||||
| chrX:105957975
|
GC | G | 1 | a0001c0001t0007 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2378delC | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 2378 | INFO_REALIGN_3_PRIME | chrX | 105957975 | ||||
| chrX:105957979
|
G | A | 1 | a0002c0002t0011 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2379G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 2379 | chrX | 105957979 | |||||
| chrX:105958290
|
TCA | T | 1 | a0010c0015t0010 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2693_*2694delCA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 2693 | INFO_REALIGN_3_PRIME | chrX | 105958290 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:105823105
|
A | G | 2 | a0003c0003t0003g0212a0003c0003t0003g0213 | 2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.57+203A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105823105 | ||||||
| chrX:105823265
|
C | T | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+363C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105823265 | ||||||
| chrX:105823296
|
T | C | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.57+394T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105823296 | ||||||
| chrX:105823337
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.57+435C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105823337 | ||||||
| chrX:105823459
|
G | A | 1 | a0008c0013t0001g0041 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.57+557G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105823459 | ||||||
| chrX:105823537
|
A | AT | 2 | a0002c0002t0002g0205a0002c0002t0002g0206 | 2 | HG00738.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.57+649dupT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105823537 | |||||
| chrX:105824145
|
T | TA | 3 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008 | 3 | HG02109.hp2 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.57+1251dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105824145 | |||||
| chrX:105824202
|
G | A | 41 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(38): Show | 42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.57+1300G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105824202 | ||||||
| chrX:105824255
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.57+1353C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105824255 | ||||||
| chrX:105824372
|
C | T | 1 | a0002c0002t0002g0206 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.57+1470C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105824372 | ||||||
| chrX:105824553
|
A | G | 1 | a0002c0002t0005g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.57+1651A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105824553 | ||||||
| chrX:105824565
|
G | A | 1 | a0006c0008t0002g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.57+1663G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105824565 | ||||||
| chrX:105824617
|
C | CA | 8 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0081others(5): Show | 8 | HG00621.hp1 HG02109.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+1732dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105824617 | |||||
| chrX:105824617
|
CA | C | 37 | a0001c0001t0001g0200a0001c0001t0004g0197a0001c0001t0004g0198others(34): Show | 37 | HG00673.hp1 HG01109.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.57+1732delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105824617 | |||||
| chrX:105824617
|
CAA | C | 47 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0046others(44): Show | 48 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.57+1731_57+1732del others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105824617 | |||||
| chrX:105824634
|
AT | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.57+1733delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105824634 | ||||||
| chrX:105824712
|
AG | A | 1 | a0001c0001t0001g0084 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.57+1812delG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105824712 | |||||
| chrX:105824792
|
G | A | 2 | a0001c0001t0004g0085a0001c0001t0004g0086 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.57+1890G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105824792 | ||||||
| chrX:105825846
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.57+2944T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105825846 | ||||||
| chrX:105825884
|
G | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(202): Show | 210 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(207): Show |
intron_variant | MODIFIER | c.57+2982G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105825884 | ||||||
| chrX:105825968
|
A | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG00735.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.57+3066A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105825968 | ||||||
| chrX:105826001
|
A | G | 1 | a0002c0002t0002g0045 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.57+3099A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826001 | ||||||
| chrX:105826038
|
G | GTC | 4 | a0002c0002t0002g0003a0002c0002t0002g0077a0002c0002t0013g0003others(1): Show | 4 | HG00741.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+3154_57+3155dup others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826038 | |||||
| chrX:105826038
|
G | GTCTC | 1 | a0001c0001t0004g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.57+3152_57+3155dup others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826038 | |||||
| chrX:105826056
|
C | A | 16 | a0001c0001t0004g0190a0002c0002t0002g0043a0002c0002t0002g0046others(13): Show | 16 | HG01358.hp1 HG01361.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.57+3154C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826056 | ||||||
| chrX:105826056
|
C | CTA | 3 | a0002c0002t0002g0058a0002c0002t0002g0059a0003c0003t0003g0033 | 3 | HG01192.hp1 HG03239.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.57+3169_57+3170dup others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826056 | |||||
| chrX:105826058
|
A | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(135): Show | 143 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(140): Show |
intron_variant | MODIFIER | c.57+3156A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826058 | ||||||
| chrX:105826060
|
A | C | 12 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0177others(9): Show | 12 | HG00621.hp1 HG00741.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.57+3158A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826060 | ||||||
| chrX:105826062
|
A | C | 1 | a0001c0001t0004g0187 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.57+3160A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826062 | ||||||
| chrX:105826147
|
TTATA | T | 1 | a0002c0002t0002g0076 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.57+3253_57+3256del others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826147 | |||||
| chrX:105826204
|
T | C | 16 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(13): Show | 16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.57+3302T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826204 | ||||||
| chrX:105826208
|
TATA | T | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+3313_57+3315del others(3): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826208 | |||||
| chrX:105826222
|
A | G | 1 | a0002c0002t0002g0057 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.57+3320A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826222 | ||||||
| chrX:105826230
|
T | TA | 1 | a0002c0002t0005g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.57+3328_57+3329ins others(1): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826230 | ||||||
| chrX:105826232
|
A | ATCATATA others(23): Show |
1 | a0001c0001t0001g0175 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.57+3350_57+3379dup others(30): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826232 | |||||
| chrX:105826249
|
T | TGATAATA others(50): Show |
3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | NA18962.hp1 NA18977.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.57+3370_57+3426dup others(57): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826249 | |||||
| chrX:105826283
|
AT | A | 1 | a0001c0001t0001g0095 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.57+3382delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826283 | ||||||
| chrX:105826291
|
TA | T | 86 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(83): Show | 87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.57+3390delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826291 | ||||||
| chrX:105826354
|
T | C | 1 | a0002c0002t0005g0199 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.57+3452T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826354 | ||||||
| chrX:105826368
|
T | TTATATAT others(43): Show |
1 | a0001c0001t0004g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.57+3499_57+3500ins others(50): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826368 | |||||
| chrX:105826391
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.57+3489A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826391 | ||||||
| chrX:105826392
|
TATATATA others(2): Show |
T | 21 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0044others(18): Show | 22 | HG00673.hp1 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.57+3500_57+3508del others(9): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826392 | |||||
| chrX:105826400
|
T | TTATATA | 2 | a0002c0002t0005g0210a0002c0002t0005g0211 | 2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.57+3498_57+3499ins others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826400 | ||||||
| chrX:105826401
|
A | AAT | 58 | a0002c0002t0002g0043a0002c0002t0002g0046a0002c0002t0002g0047others(55): Show | 58 | HG00733.hp1 HG00735.hp1 HG01071.hp2 others(55): Show |
intron_variant | MODIFIER | c.57+3510_57+3511dup others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826401 | |||||
| chrX:105826401
|
A | AATAT | 2 | a0002c0002t0005g0208a0002c0009t0005g0209 | 2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.57+3508_57+3511dup others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826401 | |||||
| chrX:105826401
|
A | AATATATT others(23): Show |
1 | a0002c0002t0005g0202 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.57+3505_57+3506ins others(30): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826401 | |||||
| chrX:105826401
|
A | AATATATT others(34): Show |
2 | a0002c0002t0005g0199a0002c0002t0011g0201 | 2 | HG02451.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.57+3505_57+3506ins others(41): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826401 | |||||
| chrX:105826401
|
A | T | 2 | a0002c0002t0005g0210a0002c0002t0005g0211 | 2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.57+3499A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826401 | ||||||
| chrX:105826827
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.57+3925A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826827 | ||||||
| chrX:105826856
|
G | A | 1 | a0002c0002t0002g0048 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.57+3954G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826856 | ||||||
| chrX:105827068
|
C | T | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.58-3986C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105827068 | ||||||
| chrX:105827676
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.58-3378G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105827676 | ||||||
| chrX:105828486
|
C | T | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-2568C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105828486 | ||||||
| chrX:105828764
|
A | G | 1 | a0002c0002t0002g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.58-2290A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105828764 | ||||||
| chrX:105829097
|
T | C | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.58-1957T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105829097 | ||||||
| chrX:105829243
|
C | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0006g0173 | 3 | HG01069.hp1 HG01071.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.58-1811C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105829243 | ||||||
| chrX:105829451
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.58-1603T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105829451 | ||||||
| chrX:105829718
|
G | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0172 | 3 | HG00609.hp1 NA18944.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.58-1336G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105829718 | ||||||
| chrX:105829828
|
C | G | 1 | a0001c0001t0004g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.58-1226C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105829828 | ||||||
| chrX:105829840
|
T | G | 41 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(38): Show | 42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.58-1214T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105829840 | ||||||
| chrX:105830224
|
C | G | 16 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(13): Show | 16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.58-830C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105830224 | ||||||
| chrX:105830238
|
CG | C | 1 | a0001c0001t0001g0101 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.58-813delG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105830238 | |||||
| chrX:105830314
|
C | CA | 4 | a0001c0001t0001g0104a0001c0001t0001g0177a0001c0001t0001g0207others(1): Show | 4 | HG00741.hp2 HG02055.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-709dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105830314 | |||||
| chrX:105830314
|
C | CAAAAA | 1 | a0002c0002t0012g0103 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.58-713_58-709dupAA others(3): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105830314 | |||||
| chrX:105830314
|
C | CAAAAAA | 1 | a0007c0010t0005g0088 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.58-714_58-709dupAA others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105830314 | |||||
| chrX:105830314
|
C | CAAAAAAA | 1 | a0002c0002t0005g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.58-715_58-709dupAA others(5): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105830314 | |||||
| chrX:105830314
|
CA | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0081others(104): Show | 111 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.58-709delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105830314 | |||||
| chrX:105830314
|
CAA | C | 40 | a0001c0001t0001g0084a0001c0001t0001g0101a0001c0001t0001g0171others(37): Show | 41 | HG00673.hp1 HG00733.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.58-710_58-709delAA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105830314 | |||||
| chrX:105830314
|
CAAA | C | 22 | a0003c0003t0003g0009a0003c0003t0003g0012a0003c0003t0003g0013others(19): Show | 22 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.58-711_58-709delAA others(1): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105830314 | |||||
| chrX:105830314
|
CAAAA | C | 10 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(7): Show | 10 | HG02109.hp2 HG02258.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.58-712_58-709delAA others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105830314 | |||||
| chrX:105830341
|
AAAAAG | A | 1 | a0002c0009t0005g0209 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.58-710_58-706delAA others(3): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105830341 | |||||
| chrX:105830342
|
AAAAG | A | 1 | a0002c0002t0005g0208 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.58-709_58-706delAG others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105830342 | |||||
| chrX:105830344
|
AAG | A | 1 | a0002c0002t0005g0211 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.58-708_58-707delGA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105830344 | |||||
| chrX:105830345
|
AG | A | 1 | a0002c0002t0005g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.58-708delG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105830345 | ||||||
| chrX:105830785
|
G | A | 1 | a0002c0002t0002g0051 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.58-269G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105830785 | ||||||
| chrX:105830841
|
A | AG | 1 | a0001c0001t0001g0101 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.58-207dupG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105830841 | |||||
| chrX:105830847
|
G | A | 1 | a0004c0004t0003g0014 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.58-207G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105830847 | ||||||
| chrX:105830982
|
TA | T | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.58-64delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105830982 | |||||
| chrX:105831740
|
T | G | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.123+621T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105831740 | ||||||
| chrX:105831745
|
TG | T | 1 | a0001c0001t0001g0101 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.123+631delG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105831745 | |||||
| chrX:105831805
|
C | T | 2 | a0002c0002t0002g0058a0002c0002t0002g0059 | 2 | HG01192.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.123+686C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105831805 | ||||||
| chrX:105832065
|
G | A | 1 | a0002c0002t0002g0048 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.123+946G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105832065 | ||||||
| chrX:105832080
|
C | G | 1 | a0001c0001t0001g0170 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.123+961C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105832080 | ||||||
| chrX:105832457
|
G | GT | 1 | a0002c0002t0012g0103 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.123+1339dupT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105832457 | |||||
| chrX:105832491
|
C | T | 1 | a0002c0002t0002g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.123+1372C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105832491 | ||||||
| chrX:105832655
|
A | G | 3 | a0002c0002t0005g0102a0002c0002t0012g0103a0007c0010t0005g0088 | 3 | HG02717.hp1 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.123+1536A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105832655 | ||||||
| chrX:105832759
|
C | G | 3 | a0001c0001t0001g0078a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | HG02683.hp2 HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.123+1640C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105832759 | ||||||
| chrX:105833058
|
C | G | 4 | a0001c0001t0004g0105a0001c0001t0004g0166a0001c0001t0004g0167others(1): Show | 4 | HG02055.hp1 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+1939C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105833058 | ||||||
| chrX:105833313
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.123+2194C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105833313 | ||||||
| chrX:105833811
|
A | G | 2 | a0001c0001t0001g0120a0001c0001t0001g0164 | 2 | NA18982.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.123+2692A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105833811 | ||||||
| chrX:105834090
|
G | A | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.123+2971G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105834090 | ||||||
| chrX:105834330
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.123+3211C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105834330 | ||||||
| chrX:105834442
|
G | GGT | 5 | a0002c0002t0005g0211a0003c0003t0003g0006a0003c0003t0003g0007others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+3329_123+3330d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105834442 | |||||
| chrX:105834450
|
C | CGT | 1 | a0001c0001t0001g0121 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.123+3352_123+3353d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105834450 | |||||
| chrX:105834450
|
C | T | 90 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(87): Show | 91 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.123+3331C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105834450 | ||||||
| chrX:105834463
|
G | A | 1 | a0002c0002t0002g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.123+3344G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105834463 | ||||||
| chrX:105834539
|
G | T | 2 | a0002c0002t0005g0199a0002c0002t0005g0202 | 2 | NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.123+3420G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105834539 | ||||||
| chrX:105834546
|
C | T | 1 | a0001c0001t0008g0079 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.123+3427C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105834546 | ||||||
| chrX:105834718
|
C | A | 1 | a0001c0001t0001g0096 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.123+3599C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105834718 | ||||||
| chrX:105835146
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.123+4027G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105835146 | ||||||
| chrX:105835241
|
T | G | 38 | a0002c0002t0011g0201a0003c0003t0003g0006a0003c0003t0003g0007others(35): Show | 38 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.123+4122T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105835241 | ||||||
| chrX:105835549
|
T | C | 1 | a0002c0002t0002g0067 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.123+4430T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105835549 | ||||||
| chrX:105835628
|
C | CT | 1 | a0007c0010t0005g0088 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.123+4524dupT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105835628 | |||||
| chrX:105835628
|
CT | C | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.123+4524delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105835628 | |||||
| chrX:105835944
|
C | T | 16 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(13): Show | 16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+4825C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105835944 | ||||||
| chrX:105835953
|
A | G | 1 | a0001c0001t0004g0190 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.123+4834A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105835953 | ||||||
| chrX:105836040
|
C | A | 1 | a0001c0001t0001g0123 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.123+4921C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105836040 | ||||||
| chrX:105836148
|
A | G | 1 | a0001c0001t0004g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.123+5029A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105836148 | ||||||
| chrX:105836455
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.123+5336A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105836455 | ||||||
| chrX:105836481
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0006g0173 | 3 | HG01069.hp1 HG01071.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.123+5362C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105836481 | ||||||
| chrX:105836520
|
A | C | 1 | a0002c0002t0005g0208 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123+5401A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105836520 | ||||||
| chrX:105836589
|
A | C | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162 | 3 | NA18986.hp1 NA18989.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.123+5470A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105836589 | ||||||
| chrX:105836682
|
T | A | 1 | a0002c0002t0002g0076 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.123+5563T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105836682 | ||||||
| chrX:105836919
|
C | T | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.123+5800C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105836919 | ||||||
| chrX:105837466
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.123+6347T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105837466 | ||||||
| chrX:105837964
|
G | C | 1 | a0001c0001t0001g0095 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.123+6845G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105837964 | ||||||
| chrX:105838727
|
C | T | 1 | a0001c0001t0004g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.123+7608C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105838727 | ||||||
| chrX:105838827
|
A | C | 3 | a0002c0002t0005g0199a0002c0002t0005g0202a0002c0002t0011g0201 | 3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.123+7708A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105838827 | ||||||
| chrX:105839252
|
A | C | 1 | a0001c0001t0001g0172 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.123+8133A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105839252 | ||||||
| chrX:105839265
|
TC | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(210): Show | 218 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(215): Show |
intron_variant | MODIFIER | c.123+8149delC | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105839265 | |||||
| chrX:105839296
|
G | C | 1 | a0001c0001t0004g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.123+8177G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105839296 | ||||||
| chrX:105839331
|
AC | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(210): Show | 218 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(215): Show |
intron_variant | MODIFIER | c.123+8216delC | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105839331 | |||||
| chrX:105839379
|
T | G | 44 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(41): Show | 45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.123+8260T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105839379 | ||||||
| chrX:105839632
|
A | T | 36 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(33): Show | 37 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.123+8513A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105839632 | ||||||
| chrX:105839765
|
G | A | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+8646G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105839765 | ||||||
| chrX:105839790
|
C | T | 3 | a0001c0001t0004g0167a0001c0001t0004g0187a0001c0001t0007g0119 | 3 | HG02723.hp1 HG03453.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.123+8671C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105839790 | ||||||
| chrX:105839821
|
G | A | 2 | a0001c0001t0004g0085a0001c0001t0004g0086 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.123+8702G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105839821 | ||||||
| chrX:105839950
|
T | C | 1 | a0002c0002t0002g0064 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.123+8831T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105839950 | ||||||
| chrX:105839987
|
G | GA | 1 | a0001c0001t0001g0104 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.123+8875dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105839987 | |||||
| chrX:105840002
|
G | A | 1 | a0003c0003t0003g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.123+8883G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105840002 | ||||||
| chrX:105840454
|
A | C | 1 | a0002c0002t0002g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.123+9335A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105840454 | ||||||
| chrX:105840463
|
A | C | 1 | a0002c0002t0002g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.123+9344A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105840463 | ||||||
| chrX:105840638
|
C | T | 3 | a0001c0001t0001g0078a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | HG02683.hp2 HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.123+9519C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105840638 | ||||||
| chrX:105840646
|
C | A | 2 | a0004c0004t0003g0015a0004c0004t0003g0016 | 2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.123+9527C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105840646 | ||||||
| chrX:105840659
|
A | G | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.123+9540A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105840659 | ||||||
| chrX:105840794
|
G | C | 5 | a0002c0002t0002g0002a0002c0002t0002g0065a0002c0002t0002g0068others(2): Show | 6 | HG02015.hp1 HG02027.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.123+9675G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105840794 | ||||||
| chrX:105840821
|
G | A | 11 | a0003c0003t0003g0012a0003c0003t0003g0024a0003c0003t0003g0025others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.123+9702G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105840821 | ||||||
| chrX:105840843
|
C | CTG | 1 | a0003c0003t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123+9736_123+9737d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105840843 | |||||
| chrX:105840855
|
G | A | 2 | a0002c0002t0002g0058a0002c0002t0002g0059 | 2 | HG01192.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.123+9736G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105840855 | ||||||
| chrX:105840855
|
G | GTA | 6 | a0001c0001t0001g0159a0002c0002t0002g0002a0002c0002t0002g0069others(3): Show | 7 | HG03098.hp1 HG03486.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+9751_123+9752d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105840855 | |||||
| chrX:105840855
|
GTA | G | 1 | a0001c0001t0001g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.123+9751_123+9752d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105840855 | |||||
| chrX:105840874
|
T | TAGAG | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.123+9762_123+9765d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105840874 | |||||
| chrX:105840874
|
TAGAG | T | 3 | a0002c0002t0005g0102a0002c0002t0012g0103a0007c0010t0005g0088 | 3 | HG02717.hp1 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.123+9762_123+9765d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105840874 | |||||
| chrX:105841879
|
A | T | 1 | a0001c0001t0001g0099 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.123+10760A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105841879 | ||||||
| chrX:105841923
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.123+10804C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105841923 | ||||||
| chrX:105842803
|
A | G | 3 | a0002c0002t0005g0199a0002c0002t0005g0202a0002c0002t0011g0201 | 3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.123+11684A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105842803 | ||||||
| chrX:105843223
|
T | G | 16 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(13): Show | 16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+12104T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105843223 | ||||||
| chrX:105843767
|
G | A | 2 | a0002c0002t0002g0003a0002c0002t0013g0003 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.123+12648G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105843767 | ||||||
| chrX:105843977
|
C | CTG | 11 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(8): Show | 11 | HG01258.hp1 HG03453.hp2 HG03490.hp1 others(8): Show |
intron_variant | MODIFIER | c.123+12898_123+1289 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105843977 | |||||
| chrX:105843977
|
C | CTGTG | 18 | a0001c0001t0004g0094a0001c0001t0004g0105a0001c0001t0004g0166others(15): Show | 18 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.123+12896_123+1289 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105843977 | |||||
| chrX:105843977
|
CTG | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0106others(8): Show | 12 | HG00609.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+12898_123+1289 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105843977 | |||||
| chrX:105843977
|
CTGTG | C | 1 | a0001c0001t0004g0197 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.123+12896_123+1289 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105843977 | |||||
| chrX:105843977
|
CTGTGTG | C | 1 | a0001c0001t0001g0126 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.123+12894_123+1289 others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105843977 | |||||
| chrX:105843977
|
CTGTGTGT others(3): Show |
C | 1 | a0001c0001t0001g0125 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.123+12890_123+1289 others(14): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105843977 | |||||
| chrX:105843987
|
G | GTC | 1 | a0002c0002t0005g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123+12869_123+1287 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105843987 | |||||
| chrX:105844011
|
G | C | 19 | a0003c0003t0003g0012a0003c0003t0003g0013a0003c0003t0003g0023others(16): Show | 19 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.123+12892G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844011 | ||||||
| chrX:105844011
|
G | GTGTGTGT others(9): Show |
1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.123+12899_123+1290 others(20): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105844011 | |||||
| chrX:105844013
|
G | C | 4 | a0002c0002t0005g0210a0002c0002t0005g0211a0003c0003t0003g0030others(1): Show | 4 | HG02109.hp1 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+12894G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844013 | ||||||
| chrX:105844015
|
G | C | 33 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0044others(30): Show | 34 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.123+12896G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844015 | ||||||
| chrX:105844015
|
G | GTC | 10 | a0002c0002t0002g0043a0002c0002t0002g0046a0002c0002t0002g0047others(7): Show | 10 | HG01192.hp1 HG01361.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.123+12897_123+1289 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105844015 | |||||
| chrX:105844017
|
G | C | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.123+12898G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844017 | ||||||
| chrX:105844017
|
GTC | G | 5 | a0002c0002t0005g0210a0002c0002t0005g0211a0003c0003t0003g0019others(2): Show | 5 | HG02109.hp1 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+12900_123+1290 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105844017 | |||||
| chrX:105844019
|
C | G | 47 | a0001c0001t0001g0184a0001c0001t0001g0200a0002c0002t0002g0002others(44): Show | 48 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.123+12900C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844019 | ||||||
| chrX:105844019
|
CTG | C | 1 | a0001c0001t0004g0193 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.123+12922_123+1292 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105844019 | |||||
| chrX:105844019
|
CTGTG | C | 19 | a0003c0003t0003g0012a0003c0003t0003g0013a0003c0003t0003g0023others(16): Show | 19 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.123+12920_123+1292 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105844019 | |||||
| chrX:105844021
|
G | C | 2 | a0001c0001t0001g0184a0002c0002t0005g0203 | 2 | NA18939.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.123+12902G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844021 | ||||||
| chrX:105844021
|
G | GTCTGTGT others(3): Show |
1 | a0005c0007t0003g0017 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.123+12903_123+1290 others(14): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105844021 | |||||
| chrX:105844023
|
G | C | 48 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(45): Show | 49 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.123+12904G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844023 | ||||||
| chrX:105844023
|
G | GTGTC | 17 | a0002c0002t0002g0063a0002c0002t0005g0199a0002c0002t0005g0202others(14): Show | 17 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.123+12907_123+1290 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105844023 | |||||
| chrX:105844035
|
G | C | 1 | a0005c0007t0003g0017 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.123+12916G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844035 | ||||||
| chrX:105844035
|
G | GTGTC | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.123+12919_123+1292 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105844035 | |||||
| chrX:105844464
|
C | T | 2 | a0003c0003t0003g0011a0003c0003t0003g0019 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.123+13345C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844464 | ||||||
| chrX:105844707
|
G | A | 1 | a0001c0001t0004g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.123+13588G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844707 | ||||||
| chrX:105844949
|
G | C | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.123+13830G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844949 | ||||||
| chrX:105845123
|
G | A | 45 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(42): Show | 46 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.123+14004G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105845123 | ||||||
| chrX:105845193
|
C | T | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.123+14074C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105845193 | ||||||
| chrX:105845454
|
G | A | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+14335G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105845454 | ||||||
| chrX:105845659
|
G | A | 1 | a0002c0002t0012g0103 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.123+14540G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105845659 | ||||||
| chrX:105845946
|
T | A | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+14827T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105845946 | ||||||
| chrX:105846034
|
A | G | 1 | a0002c0002t0011g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.123+14915A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105846034 | ||||||
| chrX:105846116
|
C | T | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.123+14997C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105846116 | ||||||
| chrX:105846468
|
G | GT | 3 | a0001c0001t0001g0121a0001c0001t0001g0204a0002c0002t0002g0045 | 3 | HG03669.hp1 HG04184.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.123+15359dupT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105846468 | |||||
| chrX:105846468
|
GT | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | NA18955.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.123+15359delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105846468 | |||||
| chrX:105846662
|
G | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | HG02683.hp2 HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.123+15543G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105846662 | ||||||
| chrX:105846936
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.123+15817G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105846936 | ||||||
| chrX:105847135
|
A | G | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.123+16016A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105847135 | ||||||
| chrX:105847140
|
A | G | 1 | a0003c0003t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.123+16021A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105847140 | ||||||
| chrX:105847403
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.123+16284C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105847403 | ||||||
| chrX:105848159
|
G | A | 45 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(42): Show | 46 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.123+17040G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105848159 | ||||||
| chrX:105848286
|
G | T | 86 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(83): Show | 87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.123+17167G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105848286 | ||||||
| chrX:105848446
|
G | T | 1 | a0003c0003t0003g0212 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.123+17327G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105848446 | ||||||
| chrX:105848659
|
A | G | 1 | a0001c0001t0001g0181 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.123+17540A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105848659 | ||||||
| chrX:105848895
|
A | T | 1 | a0001c0001t0001g0177 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.123+17776A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105848895 | ||||||
| chrX:105849068
|
A | G | 1 | a0004c0004t0003g0022 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.123+17949A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105849068 | ||||||
| chrX:105849780
|
C | T | 43 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(40): Show | 44 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.123+18661C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105849780 | ||||||
| chrX:105850261
|
C | T | 1 | a0002c0002t0002g0067 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.123+19142C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105850261 | ||||||
| chrX:105850534
|
A | G | 1 | a0002c0002t0005g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123+19415A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105850534 | ||||||
| chrX:105850816
|
TG | T | 1 | a0001c0001t0001g0091 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.123+19700delG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105850816 | |||||
| chrX:105851265
|
T | C | 1 | a0002c0002t0005g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123+20146T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105851265 | ||||||
| chrX:105851297
|
C | T | 3 | a0002c0002t0005g0199a0002c0002t0005g0202a0002c0002t0011g0201 | 3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.123+20178C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105851297 | ||||||
| chrX:105851300
|
T | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0078a0001c0001t0001g0127others(7): Show | 12 | HG00642.hp1 HG01256.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+20181T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105851300 | ||||||
| chrX:105851359
|
C | T | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.123+20240C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105851359 | ||||||
| chrX:105851718
|
C | A | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.123+20599C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105851718 | ||||||
| chrX:105851866
|
G | A | 7 | a0001c0001t0004g0090a0001c0001t0004g0092a0001c0001t0004g0094others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+20747G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105851866 | ||||||
| chrX:105851965
|
CT | C | 1 | a0001c0001t0001g0080 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.123+20847delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105851965 | ||||||
| chrX:105852109
|
T | C | 1 | a0003c0003t0003g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.123+20990T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105852109 | ||||||
| chrX:105852383
|
C | T | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+21264C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105852383 | ||||||
| chrX:105852676
|
C | G | 1 | a0002c0002t0002g0062 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.123+21557C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105852676 | ||||||
| chrX:105852829
|
G | A | 16 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(13): Show | 16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+21710G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105852829 | ||||||
| chrX:105853515
|
G | A | 44 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(41): Show | 45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.123+22396G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105853515 | ||||||
| chrX:105853928
|
A | G | 1 | a0003c0003t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123+22809A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105853928 | ||||||
| chrX:105854310
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.123+23191A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105854310 | ||||||
| chrX:105854723
|
G | A | 3 | a0002c0002t0002g0003a0002c0002t0002g0077a0002c0002t0013g0003 | 3 | HG00741.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.123+23604G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105854723 | ||||||
| chrX:105855184
|
C | T | 1 | a0001c0001t0004g0193 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.123+24065C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105855184 | ||||||
| chrX:105855212
|
A | C | 1 | a0001c0001t0001g0177 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.123+24093A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105855212 | ||||||
| chrX:105855338
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.123+24219G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105855338 | ||||||
| chrX:105855721
|
C | T | 1 | a0001c0005t0001g0004 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.124-24478C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105855721 | ||||||
| chrX:105856036
|
T | G | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-24163T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105856036 | ||||||
| chrX:105856163
|
A | C | 1 | a0002c0002t0002g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.124-24036A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105856163 | ||||||
| chrX:105856287
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.124-23912A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105856287 | ||||||
| chrX:105856308
|
A | G | 1 | a0001c0001t0004g0198 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.124-23891A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105856308 | ||||||
| chrX:105856480
|
A | G | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.124-23719A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105856480 | ||||||
| chrX:105856677
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.124-23522A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105856677 | ||||||
| chrX:105856935
|
G | T | 41 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(38): Show | 42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.124-23264G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105856935 | ||||||
| chrX:105856948
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.124-23251C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105856948 | ||||||
| chrX:105857002
|
A | T | 1 | a0003c0003t0003g0009 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.124-23197A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105857002 | ||||||
| chrX:105857071
|
A | G | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.124-23128A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105857071 | ||||||
| chrX:105857114
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0134 | 2 | NA19006.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.124-23085T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105857114 | ||||||
| chrX:105857116
|
T | C | 44 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(41): Show | 45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.124-23083T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105857116 | ||||||
| chrX:105857587
|
A | T | 41 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(38): Show | 42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.124-22612A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105857587 | ||||||
| chrX:105857689
|
T | C | 1 | a0002c0002t0002g0071 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.124-22510T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105857689 | ||||||
| chrX:105858382
|
G | GT | 55 | a0001c0001t0001g0081a0001c0001t0004g0105a0002c0002t0002g0002others(52): Show | 56 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.124-21802dupT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105858382 | |||||
| chrX:105858382
|
G | GTT | 31 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(28): Show | 31 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.124-21803_124-2180 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105858382 | |||||
| chrX:105858382
|
G | GTTT | 2 | a0003c0003t0003g0036a0005c0007t0003g0017 | 2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.124-21804_124-2180 others(7): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105858382 | |||||
| chrX:105858382
|
GT | G | 1 | a0001c0001t0001g0156 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.124-21802delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105858382 | |||||
| chrX:105858492
|
A | G | 1 | a0004c0004t0003g0022 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.124-21707A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105858492 | ||||||
| chrX:105858749
|
T | C | 1 | a0006c0008t0002g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.124-21450T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105858749 | ||||||
| chrX:105859169
|
G | GA | 1 | a0001c0005t0001g0004 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.124-21024dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105859169 | |||||
| chrX:105859323
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.124-20876T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105859323 | ||||||
| chrX:105860009
|
G | T | 1 | a0003c0003t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.124-20190G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105860009 | ||||||
| chrX:105860014
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.124-20185A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105860014 | ||||||
| chrX:105860057
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.124-20142G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105860057 | ||||||
| chrX:105860091
|
G | C | 86 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(83): Show | 87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.124-20108G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105860091 | ||||||
| chrX:105860567
|
G | GC | 1 | a0001c0001t0001g0121 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.124-19627dupC | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105860567 | |||||
| chrX:105860647
|
A | G | 2 | a0003c0003t0003g0039a0003c0003t0003g0040 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.124-19552A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105860647 | ||||||
| chrX:105860797
|
A | T | 1 | a0007c0010t0005g0088 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.124-19402A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105860797 | ||||||
| chrX:105861085
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.124-19114A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105861085 | ||||||
| chrX:105861308
|
A | G | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.124-18891A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105861308 | ||||||
| chrX:105861531
|
A | G | 1 | a0011c0006t0001g0117 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.124-18668A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105861531 | ||||||
| chrX:105861839
|
A | C | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.124-18360A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105861839 | ||||||
| chrX:105861902
|
CA | C | 86 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(83): Show | 87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.124-18286delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105861902 | |||||
| chrX:105861916
|
AGCCGGGC others(2): Show |
A | 7 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(4): Show | 7 | HG01934.hp1 HG02300.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-18281_124-1827 others(13): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105861916 | |||||
| chrX:105862041
|
C | T | 1 | a0002c0002t0005g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.124-18158C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105862041 | ||||||
| chrX:105862074
|
G | GATCT | 5 | a0001c0001t0001g0093a0001c0001t0001g0101a0001c0001t0001g0122others(2): Show | 5 | HG02080.hp2 HG02083.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-18098_124-1809 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105862074 | |||||
| chrX:105862074
|
G | GATCTATC others(1): Show |
1 | a0009c0014t0001g0135 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.124-18102_124-1809 others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105862074 | |||||
| chrX:105862074
|
GATCT | G | 86 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(83): Show | 87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.124-18098_124-1809 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105862074 | |||||
| chrX:105862074
|
GATCTATC others(1): Show |
G | 1 | a0002c0002t0002g0062 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.124-18102_124-1809 others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105862074 | |||||
| chrX:105862477
|
AT | A | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.124-17718delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105862477 | |||||
| chrX:105862684
|
T | G | 1 | a0002c0002t0005g0202 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.124-17515T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105862684 | ||||||
| chrX:105863190
|
T | A | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.124-17009T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105863190 | ||||||
| chrX:105863227
|
T | C | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.124-16972T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105863227 | ||||||
| chrX:105863321
|
G | GAC | 12 | a0001c0001t0009g0192a0002c0002t0002g0044a0002c0002t0002g0063others(9): Show | 12 | HG00140.hp1 HG00673.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.124-16842_124-1684 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863321 | |||||
| chrX:105863321
|
G | GACAC | 4 | a0002c0002t0002g0002a0002c0002t0002g0047a0002c0002t0002g0069others(1): Show | 5 | HG03710.hp1 NA18939.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-16844_124-1684 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863321 | |||||
| chrX:105863321
|
G | GACACAC | 22 | a0002c0002t0002g0003a0002c0002t0002g0043a0002c0002t0002g0045others(19): Show | 22 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.124-16846_124-1684 others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863321 | |||||
| chrX:105863321
|
G | GACACACA others(1): Show |
6 | a0002c0002t0002g0056a0002c0002t0002g0060a0002c0002t0002g0061others(3): Show | 6 | HG01515.hp1 HG02486.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-16848_124-1684 others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863321 | |||||
| chrX:105863321
|
G | GACACACA others(3): Show |
1 | a0002c0002t0002g0062 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.124-16850_124-1684 others(14): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863321 | |||||
| chrX:105863321
|
GAC | G | 3 | a0002c0002t0005g0208a0002c0002t0005g0211a0002c0009t0005g0209 | 3 | HG02809.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.124-16842_124-1684 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863321 | |||||
| chrX:105863357
|
C | CACACACA others(7): Show |
2 | a0003c0003t0003g0030a0003c0003t0003g0212 | 2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.124-16841_124-1684 others(18): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863357 | |||||
| chrX:105863357
|
C | CACACACA others(5): Show |
13 | a0003c0003t0003g0012a0003c0003t0003g0024a0003c0003t0003g0025others(10): Show | 13 | HG01884.hp2 HG02451.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.124-16841_124-1684 others(16): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863357 | |||||
| chrX:105863357
|
C | CACACACA others(3): Show |
2 | a0005c0007t0003g0017a0010c0015t0010g0176 | 2 | HG01243.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.124-16841_124-1684 others(14): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863357 | |||||
| chrX:105863357
|
C | CACACACA others(1): Show |
10 | a0001c0001t0001g0081a0001c0001t0001g0182a0003c0003t0003g0006others(7): Show | 10 | HG00621.hp1 HG01109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.124-16841_124-1684 others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863357 | |||||
| chrX:105863357
|
C | CACACAT | 14 | a0001c0001t0001g0107a0001c0001t0001g0121a0001c0001t0001g0129others(11): Show | 14 | HG01891.hp2 HG01978.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.124-16841_124-1684 others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863357 | |||||
| chrX:105863357
|
C | CACAT | 36 | a0001c0001t0001g0001a0001c0001t0001g0078a0001c0001t0001g0080others(33): Show | 38 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.124-16841_124-1684 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863357 | |||||
| chrX:105863357
|
C | CAT | 87 | a0001c0001t0001g0005a0001c0001t0001g0084a0001c0001t0001g0091others(84): Show | 89 | HG00280.hp1 HG00609.hp1 HG00733.hp2 others(86): Show |
intron_variant | MODIFIER | c.124-16840_124-1683 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863357 | |||||
| chrX:105863357
|
C | T | 4 | a0002c0002t0005g0203a0002c0002t0005g0208a0002c0002t0005g0211others(1): Show | 4 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-16842C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105863357 | ||||||
| chrX:105864157
|
G | A | 1 | a0001c0001t0004g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.124-16042G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105864157 | ||||||
| chrX:105864598
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | NA18955.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.124-15601A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105864598 | ||||||
| chrX:105864693
|
C | G | 1 | a0006c0008t0002g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.124-15506C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105864693 | ||||||
| chrX:105864908
|
GGGCTGGA others(27): Show |
G | 1 | a0003c0003t0003g0034 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.124-15289_124-1525 others(38): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105864908 | |||||
| chrX:105865110
|
C | T | 36 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(33): Show | 37 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.124-15089C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105865110 | ||||||
| chrX:105865223
|
G | C | 6 | a0001c0001t0004g0166a0001c0001t0004g0167a0001c0001t0004g0187others(3): Show | 6 | HG02486.hp1 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-14976G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105865223 | ||||||
| chrX:105865511
|
G | A | 86 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(83): Show | 87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.124-14688G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105865511 | ||||||
| chrX:105865561
|
A | AG | 1 | a0001c0001t0001g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-14637dupG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105865561 | |||||
| chrX:105865572
|
A | AG | 1 | a0001c0001t0001g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-14623dupG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105865572 | |||||
| chrX:105865647
|
T | TG | 1 | a0001c0001t0001g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-14549dupG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105865647 | |||||
| chrX:105865690
|
TG | T | 1 | a0001c0001t0001g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-14507delG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105865690 | |||||
| chrX:105865968
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-14231T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105865968 | ||||||
| chrX:105865969
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-14230C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105865969 | ||||||
| chrX:105865970
|
A | C | 1 | a0001c0001t0001g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-14229A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105865970 | ||||||
| chrX:105866014
|
C | CA | 47 | a0001c0001t0001g0116a0001c0001t0001g0121a0002c0002t0002g0002others(44): Show | 48 | HG00673.hp1 HG00733.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.124-14171dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866014 | |||||
| chrX:105866014
|
C | CAA | 4 | a0002c0002t0002g0003a0002c0002t0002g0049a0002c0002t0002g0072others(1): Show | 4 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-14172_124-1417 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866014 | |||||
| chrX:105866014
|
C | CAAA | 21 | a0003c0003t0003g0012a0003c0003t0003g0013a0003c0003t0003g0023others(18): Show | 21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.124-14173_124-1417 others(7): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866014 | |||||
| chrX:105866014
|
C | CAAAA | 16 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(13): Show | 16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.124-14174_124-1417 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866014 | |||||
| chrX:105866014
|
CA | C | 1 | a0002c0002t0005g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.124-14171delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866014 | |||||
| chrX:105866014
|
CAA | C | 1 | a0001c0001t0001g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-14172_124-1417 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866014 | |||||
| chrX:105866045
|
C | CT | 7 | a0001c0001t0001g0100a0001c0001t0001g0126a0001c0001t0001g0128others(4): Show | 7 | HG01978.hp2 NA18939.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-14148dupT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866045 | |||||
| chrX:105866130
|
AGAG | A | 1 | a0001c0001t0001g0169 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.124-14064_124-1406 others(7): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866130 | |||||
| chrX:105866217
|
TA | T | 1 | a0001c0001t0001g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-13980delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866217 | |||||
| chrX:105866261
|
CCATAATC others(203): Show |
C | 7 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(4): Show | 7 | HG01934.hp1 HG02300.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-13934_124-1372 others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866261 | |||||
| chrX:105866363
|
GA | G | 1 | a0001c0001t0001g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-13833delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866363 | |||||
| chrX:105866436
|
T | TC | 1 | a0001c0001t0001g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-13762dupC | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866436 | |||||
| chrX:105866457
|
C | A | 2 | a0002c0002t0002g0067a0002c0002t0002g0073 | 2 | HG02074.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.124-13742C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105866457 | ||||||
| chrX:105866526
|
GA | G | 1 | a0001c0001t0001g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-13671delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866526 | |||||
| chrX:105866559
|
A | G | 21 | a0003c0003t0003g0012a0003c0003t0003g0013a0003c0003t0003g0023others(18): Show | 21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.124-13640A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105866559 | ||||||
| chrX:105866588
|
CA | C | 1 | a0001c0001t0001g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-13607delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866588 | |||||
| chrX:105866843
|
G | T | 1 | a0001c0001t0001g0129 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.124-13356G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105866843 | ||||||
| chrX:105866940
|
A | G | 41 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(38): Show | 42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.124-13259A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105866940 | ||||||
| chrX:105866950
|
TC | T | 4 | a0001c0001t0001g0093a0001c0001t0001g0101a0001c0001t0001g0136others(1): Show | 4 | HG02080.hp2 HG02083.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-13247delC | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866950 | |||||
| chrX:105866972
|
C | T | 1 | a0002c0002t0002g0066 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.124-13227C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105866972 | ||||||
| chrX:105867036
|
T | C | 1 | a0002c0002t0002g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.124-13163T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105867036 | ||||||
| chrX:105867278
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0169 | 2 | HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.124-12921G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105867278 | ||||||
| chrX:105867323
|
A | G | 1 | a0002c0002t0012g0103 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.124-12876A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105867323 | ||||||
| chrX:105867369
|
G | A | 1 | a0003c0003t0003g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.124-12830G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105867369 | ||||||
| chrX:105867713
|
T | A | 1 | a0001c0001t0001g0095 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.124-12486T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105867713 | ||||||
| chrX:105867714
|
G | T | 1 | a0001c0001t0001g0095 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.124-12485G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105867714 | ||||||
| chrX:105867904
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.124-12295C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105867904 | ||||||
| chrX:105867990
|
C | CG | 1 | a0001c0001t0001g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-12209_124-1220 others(5): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105867990 | ||||||
| chrX:105868027
|
T | C | 6 | a0001c0001t0004g0090a0001c0001t0004g0092a0001c0001t0004g0094others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-12172T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105868027 | ||||||
| chrX:105868191
|
T | TG | 1 | a0001c0001t0001g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-12008_124-1200 others(5): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105868191 | ||||||
| chrX:105868220
|
A | T | 1 | a0001c0001t0001g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-11979A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105868220 | ||||||
| chrX:105868318
|
T | C | 86 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(83): Show | 87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.124-11881T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105868318 | ||||||
| chrX:105868630
|
G | C | 8 | a0004c0004t0003g0014a0004c0004t0003g0015a0004c0004t0003g0016others(5): Show | 8 | HG01243.hp1 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-11569G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105868630 | ||||||
| chrX:105868680
|
G | T | 21 | a0003c0003t0003g0012a0003c0003t0003g0013a0003c0003t0003g0023others(18): Show | 21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.124-11519G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105868680 | ||||||
| chrX:105868720
|
C | T | 16 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(13): Show | 16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.124-11479C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105868720 | ||||||
| chrX:105868721
|
G | GC | 1 | a0001c0001t0001g0155 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.124-11472dupC | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105868721 | |||||
| chrX:105868974
|
A | G | 1 | a0003c0003t0003g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.124-11225A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105868974 | ||||||
| chrX:105868975
|
C | A | 3 | a0001c0001t0004g0090a0001c0001t0004g0197a0001c0001t0004g0198 | 3 | HG01891.hp1 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.124-11224C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105868975 | ||||||
| chrX:105869028
|
A | T | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.124-11171A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105869028 | ||||||
| chrX:105869065
|
T | C | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.124-11134T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105869065 | ||||||
| chrX:105869068
|
G | A | 1 | a0001c0001t0004g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.124-11131G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105869068 | ||||||
| chrX:105869268
|
G | A | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-10931G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105869268 | ||||||
| chrX:105869549
|
C | T | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.124-10650C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105869549 | ||||||
| chrX:105869639
|
C | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(209): Show | 217 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(214): Show |
intron_variant | MODIFIER | c.124-10560C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105869639 | ||||||
| chrX:105869763
|
A | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03492.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.124-10436A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105869763 | ||||||
| chrX:105869811
|
T | TTTGATAG others(53): Show |
3 | a0002c0002t0002g0060a0002c0002t0002g0061a0002c0002t0002g0062 | 3 | HG02486.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.124-10386_124-1032 others(64): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105869811 | |||||
| chrX:105869893
|
A | G | 1 | a0002c0002t0002g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.124-10306A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105869893 | ||||||
| chrX:105869974
|
C | T | 1 | a0002c0002t0002g0052 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.124-10225C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105869974 | ||||||
| chrX:105870049
|
G | A | 7 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(4): Show | 7 | HG01934.hp1 HG02300.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-10150G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105870049 | ||||||
| chrX:105870190
|
A | G | 1 | a0002c0002t0005g0211 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.124-10009A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105870190 | ||||||
| chrX:105870636
|
T | C | 16 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(13): Show | 16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.124-9563T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105870636 | ||||||
| chrX:105870843
|
G | T | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.124-9356G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105870843 | ||||||
| chrX:105871161
|
T | C | 3 | a0002c0002t0002g0060a0002c0002t0002g0061a0002c0002t0002g0062 | 3 | HG02486.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.124-9038T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105871161 | ||||||
| chrX:105871449
|
T | C | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-8750T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105871449 | ||||||
| chrX:105871485
|
A | AAC | 38 | a0001c0001t0001g0110a0001c0001t0001g0184a0003c0003t0003g0006others(35): Show | 38 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.124-8691_124-8690d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105871485 | |||||
| chrX:105871485
|
A | AACAC | 2 | a0003c0003t0003g0010a0004c0004t0003g0016 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.124-8693_124-8690d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105871485 | |||||
| chrX:105871611
|
T | C | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.124-8588T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105871611 | ||||||
| chrX:105871633
|
G | T | 1 | a0007c0010t0005g0088 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.124-8566G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105871633 | ||||||
| chrX:105871744
|
A | T | 1 | a0001c0001t0001g0204 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.124-8455A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105871744 | ||||||
| chrX:105872029
|
A | T | 1 | a0006c0008t0002g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.124-8170A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105872029 | ||||||
| chrX:105872564
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.124-7635C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105872564 | ||||||
| chrX:105872701
|
C | G | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-7498C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105872701 | ||||||
| chrX:105872722
|
T | C | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.124-7477T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105872722 | ||||||
| chrX:105872853
|
C | T | 2 | a0003c0003t0003g0011a0003c0003t0003g0019 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.124-7346C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105872853 | ||||||
| chrX:105872900
|
G | A | 1 | a0001c0001t0004g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.124-7299G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105872900 | ||||||
| chrX:105872918
|
T | G | 1 | a0001c0001t0001g0165 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.124-7281T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105872918 | ||||||
| chrX:105873039
|
T | C | 3 | a0003c0003t0003g0038a0003c0003t0003g0039a0003c0003t0003g0040 | 3 | HG01884.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.124-7160T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105873039 | ||||||
| chrX:105873520
|
G | T | 1 | a0002c0009t0005g0209 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.124-6679G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105873520 | ||||||
| chrX:105873539
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0006g0173 | 3 | HG01069.hp1 HG01071.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.124-6660A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105873539 | ||||||
| chrX:105873619
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0099a0001c0001t0001g0106others(3): Show | 7 | HG00609.hp1 HG02135.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-6580C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105873619 | ||||||
| chrX:105873799
|
A | G | 3 | a0002c0002t0002g0060a0002c0002t0002g0061a0002c0002t0002g0062 | 3 | HG02486.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.124-6400A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105873799 | ||||||
| chrX:105873870
|
G | A | 1 | a0002c0002t0002g0064 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.124-6329G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105873870 | ||||||
| chrX:105874031
|
G | GT | 1 | a0001c0001t0001g0155 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.124-6160dupT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105874031 | |||||
| chrX:105874291
|
A | C | 1 | a0002c0002t0002g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.124-5908A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105874291 | ||||||
| chrX:105874466
|
C | G | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.124-5733C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105874466 | ||||||
| chrX:105874478
|
A | C | 3 | a0002c0002t0005g0102a0002c0002t0012g0103a0007c0010t0005g0088 | 3 | HG02717.hp1 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.124-5721A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105874478 | ||||||
| chrX:105874690
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.124-5509A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105874690 | ||||||
| chrX:105875650
|
A | T | 1 | a0002c0002t0005g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.124-4549A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105875650 | ||||||
| chrX:105875816
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.124-4383T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105875816 | ||||||
| chrX:105876225
|
TAAC | T | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.124-3971_124-3969d others(5): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105876225 | |||||
| chrX:105876310
|
A | G | 1 | a0002c0002t0002g0047 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.124-3889A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105876310 | ||||||
| chrX:105876746
|
T | G | 1 | a0001c0001t0001g0095 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.124-3453T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105876746 | ||||||
| chrX:105876763
|
T | G | 1 | a0001c0001t0004g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.124-3436T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105876763 | ||||||
| chrX:105876902
|
T | C | 1 | a0003c0003t0003g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.124-3297T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105876902 | ||||||
| chrX:105877453
|
A | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0126 | 2 | NA18965.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.124-2746A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105877453 | ||||||
| chrX:105877638
|
A | G | 11 | a0003c0003t0003g0012a0003c0003t0003g0024a0003c0003t0003g0025others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.124-2561A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105877638 | ||||||
| chrX:105877833
|
AG | A | 41 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(38): Show | 42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.124-2363delG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105877833 | |||||
| chrX:105878091
|
A | T | 1 | a0002c0002t0002g0072 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.124-2108A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105878091 | ||||||
| chrX:105878329
|
G | A | 21 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0044others(18): Show | 22 | HG00673.hp1 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.124-1870G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105878329 | ||||||
| chrX:105878497
|
T | A | 1 | a0004c0004t0003g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.124-1702T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105878497 | ||||||
| chrX:105878550
|
G | T | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.124-1649G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105878550 | ||||||
| chrX:105878570
|
C | G | 3 | a0003c0003t0003g0013a0003c0003t0003g0023a0003c0003t0003g0026 | 3 | HG01109.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.124-1629C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105878570 | ||||||
| chrX:105878642
|
G | A | 2 | a0002c0002t0005g0210a0002c0002t0005g0211 | 2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.124-1557G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105878642 | ||||||
| chrX:105878670
|
TG | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(210): Show | 218 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(215): Show |
intron_variant | MODIFIER | c.124-1527delG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105878670 | |||||
| chrX:105878677
|
A | G | 1 | a0002c0002t0002g0066 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.124-1522A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105878677 | ||||||
| chrX:105878694
|
TTTTCC | T | 1 | a0002c0002t0002g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.124-1496_124-1492d others(7): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105878694 | |||||
| chrX:105878794
|
CT | C | 1 | a0002c0002t0005g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.124-1404delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105878794 | ||||||
| chrX:105878997
|
G | A | 8 | a0004c0004t0003g0014a0004c0004t0003g0015a0004c0004t0003g0016others(5): Show | 8 | HG01243.hp1 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-1202G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105878997 | ||||||
| chrX:105879108
|
G | A | 86 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(83): Show | 87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.124-1091G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105879108 | ||||||
| chrX:105879139
|
G | A | 5 | a0001c0001t0001g0172a0002c0002t0005g0208a0002c0002t0005g0210others(2): Show | 5 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-1060G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105879139 | ||||||
| chrX:105879435
|
A | G | 3 | a0002c0002t0005g0199a0002c0002t0005g0202a0002c0002t0011g0201 | 3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.124-764A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105879435 | ||||||
| chrX:105880283
|
T | C | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.180+28T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 3/28 | chrX | 105880283 | ||||||
| chrX:105880304
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.180+49C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 3/28 | chrX | 105880304 | ||||||
| chrX:105880854
|
C | T | 1 | a0002c0002t0002g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.180+599C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 3/28 | chrX | 105880854 | ||||||
| chrX:105881153
|
TA | T | 3 | a0002c0002t0005g0199a0002c0002t0005g0202a0002c0002t0011g0201 | 3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.181-545delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chrX | 105881153 | |||||
| chrX:105881253
|
GC | G | 1 | a0008c0013t0001g0041 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.181-452delC | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chrX | 105881253 | |||||
| chrX:105881486
|
TC | T | 1 | a0008c0013t0001g0041 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.181-219delC | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chrX | 105881486 | |||||
| chrX:105881919
|
A | G | 4 | a0001c0001t0001g0099a0001c0001t0001g0106a0001c0001t0001g0179others(1): Show | 4 | HG02135.hp1 NA18984.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+140A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105881919 | ||||||
| chrX:105882252
|
A | AC | 1 | a0009c0014t0001g0135 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.252+480dupC | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chrX | 105882252 | |||||
| chrX:105882519
|
T | G | 1 | a0003c0003t0003g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.252+740T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105882519 | ||||||
| chrX:105882751
|
A | G | 1 | a0001c0005t0001g0004 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.252+972A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105882751 | ||||||
| chrX:105883065
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.252+1286A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105883065 | ||||||
| chrX:105883216
|
G | A | 6 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0137others(3): Show | 6 | NA18971.hp1 NA18986.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.252+1437G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105883216 | ||||||
| chrX:105884042
|
C | G | 9 | a0002c0002t0002g0044a0002c0002t0002g0064a0002c0002t0002g0066others(6): Show | 9 | HG00673.hp1 HG02071.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.252+2263C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105884042 | ||||||
| chrX:105884338
|
C | CT | 4 | a0001c0001t0004g0196a0002c0002t0005g0102a0002c0002t0012g0103others(1): Show | 4 | HG01168.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+2572dupT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chrX | 105884338 | |||||
| chrX:105884338
|
CT | C | 2 | a0001c0001t0001g0125a0002c0002t0002g0053 | 2 | HG02683.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.252+2572delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chrX | 105884338 | |||||
| chrX:105884353
|
C | T | 1 | a0002c0002t0005g0211 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.252+2574C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105884353 | ||||||
| chrX:105884745
|
G | A | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.252+2966G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105884745 | ||||||
| chrX:105884799
|
TTTTG | T | 1 | a0002c0002t0002g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.252+3040_252+3043d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chrX | 105884799 | |||||
| chrX:105884860
|
G | A | 1 | a0011c0006t0001g0117 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.252+3081G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105884860 | ||||||
| chrX:105884894
|
G | A | 2 | a0003c0003t0003g0024a0003c0003t0003g0029 | 2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.252+3115G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105884894 | ||||||
| chrX:105884974
|
A | G | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.252+3195A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105884974 | ||||||
| chrX:105885470
|
TGTC | T | 2 | a0003c0003t0003g0024a0003c0003t0003g0029 | 2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.253-2823_253-2821d others(5): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105885470 | ||||||
| chrX:105885686
|
CA | C | 1 | a0001c0001t0001g0156 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.253-2607delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105885686 | ||||||
| chrX:105885998
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.253-2296A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105885998 | ||||||
| chrX:105886044
|
ACATCACA others(4): Show |
A | 1 | a0011c0006t0001g0117 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.253-2248_253-2238d others(13): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chrX | 105886044 | |||||
| chrX:105886051
|
A | T | 1 | a0001c0001t0001g0131 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.253-2243A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105886051 | ||||||
| chrX:105886390
|
TACAC | T | 1 | a0001c0001t0004g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.253-1902_253-1899d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chrX | 105886390 | |||||
| chrX:105886489
|
TTA | T | 11 | a0003c0003t0003g0012a0003c0003t0003g0024a0003c0003t0003g0025others(8): Show | 11 | HG02451.hp1 HG02630.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.253-1797_253-1796d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chrX | 105886489 | |||||
| chrX:105886526
|
G | A | 5 | a0001c0001t0001g0093a0001c0001t0001g0101a0001c0001t0001g0122others(2): Show | 5 | HG02080.hp2 HG02083.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-1768G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105886526 | ||||||
| chrX:105886683
|
A | G | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.253-1611A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105886683 | ||||||
| chrX:105886832
|
A | G | 1 | a0001c0001t0001g0207 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.253-1462A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105886832 | ||||||
| chrX:105886940
|
A | G | 3 | a0002c0002t0005g0199a0002c0002t0005g0202a0002c0002t0011g0201 | 3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.253-1354A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105886940 | ||||||
| chrX:105887178
|
G | C | 1 | a0002c0002t0002g0002 | 2 | NA18939.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.253-1116G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105887178 | ||||||
| chrX:105887955
|
T | C | 2 | a0002c0002t0002g0053a0002c0002t0002g0054 | 2 | HG02683.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.253-339T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105887955 | ||||||
| chrX:105888083
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0004g0186 | 2 | HG02040.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.253-211C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105888083 | ||||||
| chrX:105888149
|
C | A | 82 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(79): Show | 83 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.253-145C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105888149 | ||||||
| chrX:105888232
|
T | C | 3 | a0001c0001t0004g0190a0001c0001t0004g0194a0001c0001t0004g0195 | 3 | HG00280.hp1 HG01358.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.253-62T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105888232 | ||||||
| chrX:105888694
|
C | T | 1 | a0002c0002t0005g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.378+275C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105888694 | ||||||
| chrX:105888695
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.378+276G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105888695 | ||||||
| chrX:105888724
|
G | A | 21 | a0003c0003t0003g0012a0003c0003t0003g0013a0003c0003t0003g0023others(18): Show | 21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.378+305G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105888724 | ||||||
| chrX:105888831
|
C | T | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+412C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105888831 | ||||||
| chrX:105888832
|
G | A | 3 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008 | 3 | HG02109.hp2 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.378+413G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105888832 | ||||||
| chrX:105888835
|
C | T | 1 | a0003c0003t0003g0009 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.378+416C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105888835 | ||||||
| chrX:105889115
|
G | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG03492.hp1 HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.378+696G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105889115 | ||||||
| chrX:105889345
|
C | G | 82 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(79): Show | 83 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.378+926C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105889345 | ||||||
| chrX:105889351
|
G | GC | 213 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(210): Show | 218 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(215): Show |
intron_variant | MODIFIER | c.378+933dupC | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chrX | 105889351 | |||||
| chrX:105889382
|
TTGAG | T | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.378+966_378+969del others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chrX | 105889382 | |||||
| chrX:105889570
|
T | C | 86 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(83): Show | 87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.378+1151T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105889570 | ||||||
| chrX:105889591
|
GC | G | 1 | a0001c0001t0001g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.378+1174delC | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chrX | 105889591 | |||||
| chrX:105889594
|
T | C | 3 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008 | 3 | HG02109.hp2 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.378+1175T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105889594 | ||||||
| chrX:105889611
|
C | G | 1 | a0001c0001t0001g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.378+1192C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105889611 | ||||||
| chrX:105890323
|
A | C | 2 | a0002c0002t0005g0210a0002c0002t0005g0211 | 2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.378+1904A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105890323 | ||||||
| chrX:105890913
|
G | T | 1 | a0003c0003t0003g0009 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.378+2494G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105890913 | ||||||
| chrX:105891085
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.378+2666G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105891085 | ||||||
| chrX:105891086
|
C | A | 1 | a0001c0001t0001g0155 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.378+2667C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105891086 | ||||||
| chrX:105891904
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0006g0173 | 3 | HG01069.hp1 HG01071.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.379-1928G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105891904 | ||||||
| chrX:105892195
|
A | C | 1 | a0011c0006t0001g0117 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.379-1637A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105892195 | ||||||
| chrX:105892551
|
A | G | 6 | a0001c0001t0001g0005a0001c0001t0001g0099a0001c0001t0001g0106others(3): Show | 7 | HG00609.hp1 HG02135.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-1281A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105892551 | ||||||
| chrX:105892732
|
T | C | 4 | a0002c0002t0002g0049a0002c0002t0002g0050a0002c0002t0002g0051others(1): Show | 4 | HG00735.hp1 HG01071.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-1100T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105892732 | ||||||
| chrX:105892745
|
G | A | 2 | a0002c0002t0005g0208a0002c0009t0005g0209 | 2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.379-1087G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105892745 | ||||||
| chrX:105892797
|
C | T | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.379-1035C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105892797 | ||||||
| chrX:105893221
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.379-611A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105893221 | ||||||
| chrX:105893246
|
C | G | 1 | a0002c0002t0005g0202 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.379-586C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105893246 | ||||||
| chrX:105893261
|
C | A | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.379-571C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105893261 | ||||||
| chrX:105893693
|
A | C | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.379-139A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105893693 | ||||||
| chrX:105894114
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.489+172C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | chrX | 105894114 | ||||||
| chrX:105894228
|
T | C | 2 | a0004c0004t0003g0020a0004c0004t0003g0021 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.489+286T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | chrX | 105894228 | ||||||
| chrX:105894314
|
G | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0126a0001c0001t0001g0128 | 3 | NA18965.hp1 NA19063.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.489+372G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | chrX | 105894314 | ||||||
| chrX:105894502
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.489+560A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | chrX | 105894502 | ||||||
| chrX:105894579
|
G | A | 3 | a0002c0002t0005g0199a0002c0002t0005g0202a0002c0002t0011g0201 | 3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.489+637G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | chrX | 105894579 | ||||||
| chrX:105894835
|
G | C | 1 | a0001c0001t0001g0204 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.490-598G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | chrX | 105894835 | ||||||
| chrX:105894946
|
G | A | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.490-487G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | chrX | 105894946 | ||||||
| chrX:105894960
|
C | A | 3 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008 | 3 | HG02109.hp2 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.490-473C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | chrX | 105894960 | ||||||
| chrX:105895363
|
C | CAGAA | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0108others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.490-40_490-37dupGA others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chrX | 105895363 | |||||
| chrX:105895363
|
C | CAGAAAGA others(1): Show |
2 | a0001c0001t0001g0174a0002c0002t0011g0201 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.490-44_490-37dupGA others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chrX | 105895363 | |||||
| chrX:105895363
|
CAGAA | C | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.490-40_490-37delGA others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chrX | 105895363 | |||||
| chrX:105895363
|
CAGAAAGA others(5): Show |
C | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-48_490-37delGA others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chrX | 105895363 | |||||
| chrX:105895417
|
TA | T | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.490-10delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chrX | 105895417 | |||||
| chrX:105895686
|
AGAGGAG | A | 1 | a0001c0001t0001g0162 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.580+165_580+170del others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chrX | 105895686 | |||||
| chrX:105895938
|
CA | C | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.580+418delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chrX | 105895938 | |||||
| chrX:105896248
|
A | C | 1 | a0005c0007t0003g0017 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.580+725A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105896248 | ||||||
| chrX:105896434
|
G | A | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.580+911G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105896434 | ||||||
| chrX:105896447
|
A | G | 1 | a0001c0001t0004g0187 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.580+924A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105896447 | ||||||
| chrX:105896676
|
C | CA | 1 | a0001c0001t0001g0162 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.580+1163dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chrX | 105896676 | |||||
| chrX:105896724
|
TC | T | 1 | a0001c0001t0001g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.580+1204delC | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chrX | 105896724 | |||||
| chrX:105896786
|
T | TAA | 1 | a0002c0002t0002g0062 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.580+1265_580+1266d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chrX | 105896786 | |||||
| chrX:105896924
|
ATAGT | A | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.580+1404_580+1407d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chrX | 105896924 | |||||
| chrX:105897068
|
A | C | 3 | a0002c0002t0005g0199a0002c0002t0005g0202a0002c0002t0011g0201 | 3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.581-1516A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105897068 | ||||||
| chrX:105897126
|
ATTAGAGT | A | 1 | a0002c0002t0005g0202 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.581-1454_581-1448d others(9): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chrX | 105897126 | |||||
| chrX:105897243
|
C | A | 1 | a0001c0001t0001g0154 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.581-1341C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105897243 | ||||||
| chrX:105897269
|
AT | A | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.581-1310delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chrX | 105897269 | |||||
| chrX:105897359
|
A | AG | 1 | a0001c0001t0001g0162 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.581-1222dupG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chrX | 105897359 | |||||
| chrX:105897372
|
G | GA | 1 | a0001c0001t0001g0162 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.581-1207dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chrX | 105897372 | |||||
| chrX:105897410
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.581-1174C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105897410 | ||||||
| chrX:105897498
|
T | TTC | 1 | a0001c0001t0001g0162 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.581-1082_581-1081d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chrX | 105897498 | |||||
| chrX:105897508
|
C | CT | 1 | a0001c0001t0001g0162 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.581-1070dupT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chrX | 105897508 | |||||
| chrX:105897518
|
T | G | 3 | a0002c0002t0005g0199a0002c0002t0005g0202a0002c0002t0011g0201 | 3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.581-1066T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105897518 | ||||||
| chrX:105897755
|
G | A | 3 | a0002c0002t0005g0199a0002c0002t0005g0202a0002c0002t0011g0201 | 3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.581-829G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105897755 | ||||||
| chrX:105898024
|
G | T | 2 | a0002c0002t0005g0210a0002c0002t0005g0211 | 2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.581-560G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105898024 | ||||||
| chrX:105898500
|
G | T | 1 | a0002c0002t0002g0067 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.581-84G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105898500 | ||||||
| chrX:105898521
|
G | A | 2 | a0002c0002t0005g0210a0002c0002t0005g0211 | 2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.581-63G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105898521 | ||||||
| chrX:105898915
|
G | A | 44 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(41): Show | 45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.711+201G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | chrX | 105898915 | ||||||
| chrX:105899005
|
A | C | 4 | a0001c0001t0001g0093a0001c0001t0001g0101a0001c0001t0001g0136others(1): Show | 4 | HG02080.hp2 HG02083.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.711+291A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | chrX | 105899005 | ||||||
| chrX:105899038
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0169 | 2 | HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.711+324G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | chrX | 105899038 | ||||||
| chrX:105899646
|
T | C | 1 | a0001c0001t0004g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.711+932T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | chrX | 105899646 | ||||||
| chrX:105899827
|
G | T | 3 | a0002c0002t0005g0102a0002c0002t0012g0103a0007c0010t0005g0088 | 3 | HG02717.hp1 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.712-791G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | chrX | 105899827 | ||||||
| chrX:105899832
|
G | C | 1 | a0001c0001t0001g0148 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.712-786G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | chrX | 105899832 | ||||||
| chrX:105899957
|
G | A | 1 | a0003c0003t0003g0009 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.712-661G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | chrX | 105899957 | ||||||
| chrX:105900151
|
T | TAC | 33 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0099others(30): Show | 34 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.712-425_712-424dup others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chrX | 105900151 | |||||
| chrX:105900151
|
T | TACAC | 7 | a0001c0001t0001g0078a0002c0002t0002g0044a0002c0002t0002g0046others(4): Show | 7 | HG00673.hp1 HG00733.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.712-427_712-424dup others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chrX | 105900151 | |||||
| chrX:105900151
|
T | TACACAC | 4 | a0001c0001t0001g0185a0002c0002t0002g0074a0002c0002t0005g0102others(1): Show | 4 | HG02976.hp2 HG03130.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.712-429_712-424dup others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chrX | 105900151 | |||||
| chrX:105900151
|
TAC | T | 17 | a0001c0001t0001g0093a0001c0001t0001g0101a0001c0001t0001g0109others(14): Show | 17 | HG01071.hp2 HG02080.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.712-425_712-424del others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chrX | 105900151 | |||||
| chrX:105900151
|
TACAC | T | 10 | a0001c0001t0001g0100a0001c0001t0001g0151a0001c0001t0001g0164others(7): Show | 10 | HG01074.hp1 HG02451.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.712-427_712-424del others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chrX | 105900151 | |||||
| chrX:105900151
|
TACACAC | T | 3 | a0001c0001t0001g0157a0001c0001t0001g0161a0002c0009t0005g0209 | 3 | HG02809.hp2 HG04204.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.712-429_712-424del others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chrX | 105900151 | |||||
| chrX:105900151
|
TACACACA others(1): Show |
T | 1 | a0003c0003t0003g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.712-431_712-424del others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chrX | 105900151 | |||||
| chrX:105900151
|
TACACACA others(3): Show |
T | 15 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(12): Show | 15 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.712-433_712-424del others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chrX | 105900151 | |||||
| chrX:105900151
|
TACACACA others(5): Show |
T | 21 | a0003c0003t0003g0012a0003c0003t0003g0013a0003c0003t0003g0023others(18): Show | 21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.712-435_712-424del others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chrX | 105900151 | |||||
| chrX:105900747
|
C | T | 8 | a0004c0004t0003g0014a0004c0004t0003g0015a0004c0004t0003g0016others(5): Show | 8 | HG01243.hp1 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.766+75C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105900747 | ||||||
| chrX:105900823
|
G | A | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+151G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105900823 | ||||||
| chrX:105900913
|
A | G | 3 | a0002c0002t0005g0199a0002c0002t0005g0202a0002c0002t0011g0201 | 3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.766+241A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105900913 | ||||||
| chrX:105901011
|
G | A | 86 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(83): Show | 87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.766+339G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105901011 | ||||||
| chrX:105901150
|
G | GT | 1 | a0001c0001t0001g0083 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.766+488dupT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | INFO_REALIGN_3_PRIME | chrX | 105901150 | |||||
| chrX:105901795
|
A | C | 1 | a0001c0001t0001g0169 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.766+1123A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105901795 | ||||||
| chrX:105901966
|
T | C | 2 | a0002c0002t0005g0210a0002c0002t0005g0211 | 2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.766+1294T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105901966 | ||||||
| chrX:105902355
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.766+1683C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105902355 | ||||||
| chrX:105902444
|
G | A | 1 | a0002c0002t0002g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.766+1772G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105902444 | ||||||
| chrX:105902559
|
C | A | 1 | a0007c0010t0005g0088 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.766+1887C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105902559 | ||||||
| chrX:105903073
|
A | G | 1 | a0002c0002t0005g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.767-2192A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105903073 | ||||||
| chrX:105903562
|
C | G | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.767-1703C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105903562 | ||||||
| chrX:105903700
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.767-1565T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105903700 | ||||||
| chrX:105903841
|
C | T | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-1424C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105903841 | ||||||
| chrX:105903880
|
G | T | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.767-1385G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105903880 | ||||||
| chrX:105904766
|
G | T | 1 | a0002c0002t0002g0044 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.767-499G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105904766 | ||||||
| chrX:105904823
|
G | C | 41 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(38): Show | 42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.767-442G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105904823 | ||||||
| chrX:105905247
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.767-18A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105905247 | ||||||
| chrX:105905755
|
T | A | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.845+412T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 10/28 | chrX | 105905755 | ||||||
| chrX:105906764
|
C | CGT | 19 | a0001c0001t0001g0099a0001c0001t0001g0114a0001c0001t0001g0115others(16): Show | 19 | HG00735.hp2 HG01981.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1021+218_1021+219d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | |||||
| chrX:105906764
|
C | CGTGT | 14 | a0002c0002t0002g0002a0002c0002t0002g0045a0002c0002t0002g0049others(11): Show | 15 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1021+216_1021+219d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | |||||
| chrX:105906764
|
C | CGTGTGT | 15 | a0001c0001t0001g0106a0001c0001t0001g0189a0002c0002t0002g0003others(12): Show | 15 | HG01099.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1021+214_1021+219d others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | |||||
| chrX:105906764
|
C | CGTGTGTG others(1): Show |
8 | a0001c0001t0001g0151a0002c0002t0002g0043a0002c0002t0002g0046others(5): Show | 8 | HG00733.hp1 HG01361.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021+212_1021+219d others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | |||||
| chrX:105906764
|
C | CGTGTGTG others(3): Show |
1 | a0002c0002t0002g0055 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1021+210_1021+219d others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | |||||
| chrX:105906764
|
C | CGTGTGTG others(5): Show |
1 | a0002c0002t0002g0059 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1021+208_1021+219d others(14): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | |||||
| chrX:105906764
|
CGT | C | 25 | a0001c0001t0001g0104a0001c0001t0001g0110a0001c0001t0001g0125others(22): Show | 25 | HG00280.hp1 HG01358.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1021+218_1021+219d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | |||||
| chrX:105906764
|
CGTGT | C | 17 | a0001c0001t0001g0141a0001c0001t0001g0182a0002c0002t0002g0044others(14): Show | 17 | HG00673.hp1 HG01243.hp1 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1021+216_1021+219d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | |||||
| chrX:105906764
|
CGTGTGT | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0078a0001c0001t0001g0080others(27): Show | 33 | HG00621.hp1 HG00642.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1021+214_1021+219d others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | |||||
| chrX:105906764
|
CGTGTGTG others(1): Show |
C | 23 | a0001c0001t0001g0134a0001c0001t0001g0158a0001c0001t0001g0159others(20): Show | 23 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.1021+212_1021+219d others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | |||||
| chrX:105907040
|
G | A | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1021+451G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | chrX | 105907040 | ||||||
| chrX:105907109
|
A | G | 1 | a0002c0002t0002g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1021+520A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | chrX | 105907109 | ||||||
| chrX:105907352
|
G | A | 1 | a0003c0003t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1021+763G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | chrX | 105907352 | ||||||
| chrX:105907672
|
C | T | 25 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0044others(22): Show | 26 | HG00673.hp1 HG00735.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.1022-568C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | chrX | 105907672 | ||||||
| chrX:105907942
|
T | TCATTCTC others(9): Show |
1 | a0001c0001t0001g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1022-290_1022-275d others(18): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105907942 | |||||
| chrX:105908114
|
G | A | 1 | a0002c0002t0002g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1022-126G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | chrX | 105908114 | ||||||
| chrX:105908369
|
C | T | 2 | a0002c0002t0005g0199a0002c0002t0005g0202 | 2 | NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1085+66C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 12/28 | chrX | 105908369 | ||||||
| chrX:105910166
|
TA | T | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2241+289delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chrX | 105910166 | |||||
| chrX:105910171
|
A | G | 16 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(13): Show | 16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2241+289A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105910171 | ||||||
| chrX:105910516
|
C | T | 82 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(79): Show | 83 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.2241+634C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105910516 | ||||||
| chrX:105910529
|
C | T | 1 | a0009c0014t0001g0135 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2241+647C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105910529 | ||||||
| chrX:105910782
|
T | G | 1 | a0001c0001t0001g0080 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2241+900T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105910782 | ||||||
| chrX:105911288
|
C | A | 1 | a0003c0003t0003g0031 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2242-1360C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105911288 | ||||||
| chrX:105911407
|
T | A | 1 | a0002c0002t0002g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2242-1241T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105911407 | ||||||
| chrX:105911796
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2242-852A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105911796 | ||||||
| chrX:105911836
|
G | A | 1 | a0001c0001t0004g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2242-812G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105911836 | ||||||
| chrX:105911849
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2242-799G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105911849 | ||||||
| chrX:105911882
|
C | T | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.2242-766C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105911882 | ||||||
| chrX:105911884
|
A | G | 3 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008 | 3 | HG02109.hp2 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2242-764A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105911884 | ||||||
| chrX:105912426
|
GCATTTCT | G | 1 | a0002c0002t0002g0074 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2242-219_2242-213d others(9): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chrX | 105912426 | |||||
| chrX:105912506
|
A | G | 7 | a0003c0003t0003g0031a0003c0003t0003g0032a0003c0003t0003g0036others(4): Show | 7 | HG01884.hp2 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2242-142A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105912506 | ||||||
| chrX:105912539
|
A | G | 1 | a0002c0002t0005g0199 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2242-109A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105912539 | ||||||
| chrX:105912976
|
A | C | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2349+221A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105912976 | ||||||
| chrX:105913171
|
A | T | 1 | a0001c0001t0001g0136 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2349+416A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105913171 | ||||||
| chrX:105913328
|
T | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0125 | 2 | HG01952.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.2349+573T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105913328 | ||||||
| chrX:105913663
|
G | A | 11 | a0002c0002t0002g0043a0002c0002t0002g0046a0002c0002t0002g0047others(8): Show | 11 | HG00733.hp1 HG01192.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.2349+908G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105913663 | ||||||
| chrX:105913731
|
A | G | 44 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(41): Show | 45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.2349+976A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105913731 | ||||||
| chrX:105913937
|
T | G | 1 | a0002c0002t0002g0062 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2349+1182T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105913937 | ||||||
| chrX:105914080
|
G | GA | 1 | a0001c0001t0001g0121 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2349+1326dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chrX | 105914080 | |||||
| chrX:105914292
|
T | A | 86 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(83): Show | 87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.2350-1438T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105914292 | ||||||
| chrX:105914377
|
G | T | 1 | a0001c0001t0001g0121 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2350-1353G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105914377 | ||||||
| chrX:105914491
|
TC | T | 1 | a0001c0001t0001g0121 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2350-1235delC | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chrX | 105914491 | |||||
| chrX:105914510
|
A | G | 21 | a0003c0003t0003g0012a0003c0003t0003g0013a0003c0003t0003g0023others(18): Show | 21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.2350-1220A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105914510 | ||||||
| chrX:105914636
|
T | TG | 1 | a0001c0001t0001g0121 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2350-1091dupG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chrX | 105914636 | |||||
| chrX:105914714
|
G | A | 2 | a0001c0001t0001g0095a0002c0002t0011g0201 | 2 | HG02040.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2350-1016G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105914714 | ||||||
| chrX:105914726
|
G | A | 1 | a0001c0001t0004g0105 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2350-1004G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105914726 | ||||||
| chrX:105914750
|
A | AAG | 1 | a0001c0001t0001g0121 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2350-980_2350-979i others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105914750 | ||||||
| chrX:105914751
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2350-979G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105914751 | ||||||
| chrX:105914826
|
T | TA | 1 | a0001c0001t0001g0121 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2350-898dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chrX | 105914826 | |||||
| chrX:105914939
|
G | GT | 1 | a0001c0001t0001g0121 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2350-790dupT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chrX | 105914939 | |||||
| chrX:105914999
|
G | GAA | 1 | a0001c0001t0001g0121 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2350-729_2350-728d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chrX | 105914999 | |||||
| chrX:105915004
|
T | TA | 1 | a0001c0001t0001g0121 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2350-722dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chrX | 105915004 | |||||
| chrX:105915544
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2350-186A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105915544 | ||||||
| chrX:105916328
|
A | G | 1 | a0001c0001t0004g0198 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2417+531A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105916328 | ||||||
| chrX:105916381
|
A | G | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2417+584A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105916381 | ||||||
| chrX:105916423
|
T | A | 109 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0090others(106): Show | 110 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(107): Show |
intron_variant | MODIFIER | c.2417+626T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105916423 | ||||||
| chrX:105916589
|
A | G | 1 | a0003c0003t0003g0028 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2417+792A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105916589 | ||||||
| chrX:105916662
|
C | T | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.2417+865C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105916662 | ||||||
| chrX:105916702
|
T | C | 44 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(41): Show | 45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.2418-876T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105916702 | ||||||
| chrX:105916879
|
T | A | 4 | a0001c0001t0001g0099a0001c0001t0001g0106a0001c0001t0001g0179others(1): Show | 4 | HG02135.hp1 NA18984.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.2418-699T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105916879 | ||||||
| chrX:105916930
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2418-648C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105916930 | ||||||
| chrX:105917042
|
C | T | 2 | a0001c0001t0004g0197a0001c0001t0004g0198 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2418-536C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105917042 | ||||||
| chrX:105917145
|
C | T | 21 | a0003c0003t0003g0012a0003c0003t0003g0013a0003c0003t0003g0023others(18): Show | 21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.2418-433C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105917145 | ||||||
| chrX:105917181
|
A | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0126a0001c0001t0001g0128 | 3 | NA18965.hp1 NA19063.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2418-397A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105917181 | ||||||
| chrX:105917188
|
A | T | 44 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(41): Show | 45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.2418-390A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105917188 | ||||||
| chrX:105917270
|
T | TA | 1 | a0001c0001t0001g0121 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2418-304dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | INFO_REALIGN_3_PRIME | chrX | 105917270 | |||||
| chrX:105917926
|
CG | C | 1 | a0006c0008t0002g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2512+260delG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105917926 | |||||
| chrX:105917986
|
T | C | 1 | a0002c0002t0002g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2512+314T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105917986 | ||||||
| chrX:105918394
|
T | TA | 1 | a0001c0001t0001g0121 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2512+727dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105918394 | |||||
| chrX:105918448
|
TG | T | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2512+777delG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105918448 | ||||||
| chrX:105918734
|
T | TG | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2512+1064dupG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105918734 | |||||
| chrX:105918780
|
C | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0113 | 2 | HG02129.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.2512+1108C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105918780 | ||||||
| chrX:105918889
|
TG | T | 3 | a0002c0002t0005g0199a0002c0002t0005g0202a0002c0002t0011g0201 | 3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.2512+1219delG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105918889 | |||||
| chrX:105919002
|
G | GA | 10 | a0001c0001t0001g0080a0001c0001t0001g0121a0001c0001t0001g0134others(7): Show | 10 | HG01978.hp2 HG01981.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2512+1352dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105919002 | |||||
| chrX:105919002
|
G | GAA | 1 | a0001c0001t0001g0109 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2512+1351_2512+135 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105919002 | |||||
| chrX:105919002
|
GA | G | 76 | a0001c0001t0001g0108a0001c0001t0001g0164a0001c0001t0001g0184others(73): Show | 76 | HG00673.hp1 HG00733.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.2512+1352delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105919002 | |||||
| chrX:105919002
|
GAA | G | 7 | a0002c0002t0002g0002a0002c0002t0002g0060a0002c0002t0002g0061others(4): Show | 8 | HG01515.hp1 HG02486.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2512+1351_2512+135 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105919002 | |||||
| chrX:105919055
|
A | G | 16 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(13): Show | 16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2512+1383A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105919055 | ||||||
| chrX:105919385
|
A | G | 44 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(41): Show | 45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.2512+1713A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105919385 | ||||||
| chrX:105919392
|
A | G | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2512+1720A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105919392 | ||||||
| chrX:105919446
|
C | T | 1 | a0002c0002t0005g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2512+1774C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105919446 | ||||||
| chrX:105919458
|
A | C | 1 | a0002c0002t0002g0043 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2512+1786A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105919458 | ||||||
| chrX:105919492
|
TA | T | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2512+1824delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105919492 | |||||
| chrX:105919536
|
A | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0078a0001c0001t0001g0080others(29): Show | 34 | HG00621.hp1 HG00642.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.2512+1864A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105919536 | ||||||
| chrX:105919769
|
GT | G | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2512+2099delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105919769 | |||||
| chrX:105920231
|
C | G | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2513-1733C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920231 | ||||||
| chrX:105920260
|
T | C | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.2513-1704T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920260 | ||||||
| chrX:105920272
|
T | C | 1 | a0001c0005t0001g0004 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2513-1692T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920272 | ||||||
| chrX:105920318
|
G | C | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.2513-1646G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920318 | ||||||
| chrX:105920476
|
AC | A | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2513-1486delC | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105920476 | |||||
| chrX:105920589
|
C | A | 2 | a0003c0003t0003g0039a0003c0003t0003g0040 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2513-1375C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920589 | ||||||
| chrX:105920648
|
AC | A | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2513-1312delC | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105920648 | |||||
| chrX:105920666
|
C | T | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2513-1298C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920666 | ||||||
| chrX:105920766
|
CA | C | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2513-1194delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105920766 | |||||
| chrX:105920786
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2513-1178A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920786 | ||||||
| chrX:105920814
|
TA | T | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2513-1145delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105920814 | |||||
| chrX:105920875
|
T | C | 16 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(13): Show | 16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2513-1089T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920875 | ||||||
| chrX:105920924
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2513-1040G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920924 | ||||||
| chrX:105920981
|
G | C | 1 | a0001c0001t0001g0152 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2513-983G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920981 | ||||||
| chrX:105921095
|
T | C | 1 | a0002c0002t0002g0066 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2513-869T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921095 | ||||||
| chrX:105921098
|
T | C | 1 | a0002c0002t0002g0206 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2513-866T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921098 | ||||||
| chrX:105921105
|
G | C | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2513-859G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921105 | ||||||
| chrX:105921286
|
T | TGGA | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2513-678_2513-677i others(5): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921286 | ||||||
| chrX:105921290
|
AT | A | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2513-673delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921290 | ||||||
| chrX:105921336
|
T | TG | 1 | a0001c0001t0001g0182 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2513-622dupG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105921336 | |||||
| chrX:105921398
|
G | C | 21 | a0003c0003t0003g0012a0003c0003t0003g0013a0003c0003t0003g0023others(18): Show | 21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.2513-566G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921398 | ||||||
| chrX:105921404
|
T | C | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.2513-560T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921404 | ||||||
| chrX:105921405
|
G | A | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.2513-559G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921405 | ||||||
| chrX:105921482
|
TA | T | 2 | a0002c0002t0002g0206a0002c0002t0005g0208 | 2 | HG00738.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2513-470delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105921482 | |||||
| chrX:105921520
|
A | G | 4 | a0002c0002t0002g0049a0002c0002t0002g0050a0002c0002t0002g0051others(1): Show | 4 | HG00735.hp1 HG01071.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.2513-444A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921520 | ||||||
| chrX:105921564
|
G | A | 1 | a0003c0003t0003g0213 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2513-400G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921564 | ||||||
| chrX:105921855
|
C | CA | 36 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(33): Show | 36 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.2513-107dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105921855 | |||||
| chrX:105921858
|
G | A | 82 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(79): Show | 83 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.2513-106G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921858 | ||||||
| chrX:105921858
|
G | GA | 1 | a0001c0001t0001g0121 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2513-95dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105921858 | |||||
| chrX:105922147
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2610+86G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 17/28 | chrX | 105922147 | ||||||
| chrX:105922150
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2610+89A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 17/28 | chrX | 105922150 | ||||||
| chrX:105922152
|
G | T | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2610+91G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 17/28 | chrX | 105922152 | ||||||
| chrX:105922560
|
A | C | 1 | a0001c0001t0001g0126 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2610+499A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 17/28 | chrX | 105922560 | ||||||
| chrX:105922775
|
AG | A | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2611-339delG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chrX | 105922775 | |||||
| chrX:105922803
|
C | G | 2 | a0002c0002t0002g0044a0002c0002t0002g0076 | 2 | HG00673.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.2611-315C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 17/28 | chrX | 105922803 | ||||||
| chrX:105923081
|
C | CTA | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2611-36_2611-35dup others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chrX | 105923081 | |||||
| chrX:105923487
|
GT | G | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2975+12delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923487 | |||||
| chrX:105923574
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2975+92G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | chrX | 105923574 | ||||||
| chrX:105923591
|
T | A | 21 | a0003c0003t0003g0012a0003c0003t0003g0013a0003c0003t0003g0023others(18): Show | 21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.2975+109T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | chrX | 105923591 | ||||||
| chrX:105923634
|
A | G | 1 | a0002c0002t0011g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2975+152A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | chrX | 105923634 | ||||||
| chrX:105923891
|
C | CTA | 15 | a0001c0001t0001g0078a0001c0001t0001g0087a0001c0001t0001g0118others(12): Show | 15 | HG01168.hp2 HG02056.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2975+443_2975+444d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | |||||
| chrX:105923891
|
C | CTATA | 12 | a0001c0001t0001g0124a0001c0001t0001g0137a0001c0001t0001g0141others(9): Show | 12 | HG00741.hp1 HG01071.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.2975+441_2975+444d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | |||||
| chrX:105923891
|
C | CTATATA | 17 | a0001c0001t0001g0095a0001c0001t0001g0168a0001c0001t0001g0180others(14): Show | 18 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.2975+439_2975+444d others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | |||||
| chrX:105923891
|
C | CTATATAT others(1): Show |
19 | a0002c0002t0002g0043a0002c0002t0002g0045a0002c0002t0002g0047others(16): Show | 19 | HG00735.hp1 HG00738.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.2975+437_2975+444d others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | |||||
| chrX:105923891
|
C | CTATATAT others(3): Show |
5 | a0001c0001t0004g0193a0002c0002t0002g0046a0002c0002t0002g0067others(2): Show | 5 | HG01884.hp1 HG02809.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.2975+435_2975+444d others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | |||||
| chrX:105923891
|
C | CTATATAT others(5): Show |
4 | a0002c0002t0002g0051a0002c0002t0002g0058a0002c0002t0002g0069others(1): Show | 4 | HG03041.hp2 HG03239.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.2975+433_2975+444d others(14): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | |||||
| chrX:105923891
|
C | CTATATAT others(9): Show |
1 | a0001c0001t0001g0152 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2975+429_2975+444d others(18): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | |||||
| chrX:105923891
|
C | CTATATAT others(11): Show |
1 | a0002c0002t0002g0059 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2975+427_2975+444d others(20): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | |||||
| chrX:105923891
|
CTA | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0084a0001c0001t0001g0093others(57): Show | 62 | HG00609.hp1 HG00735.hp2 HG01074.hp1 others(59): Show |
intron_variant | MODIFIER | c.2975+443_2975+444d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | |||||
| chrX:105923891
|
CTATA | C | 6 | a0001c0001t0001g0116a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG01934.hp1 HG02300.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2975+441_2975+444d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | |||||
| chrX:105923891
|
CTATATA | C | 2 | a0002c0002t0005g0102a0007c0010t0005g0088 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2975+439_2975+444d others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | |||||
| chrX:105923902
|
TA | T | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2975+421delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | chrX | 105923902 | ||||||
| chrX:105923907
|
ATATATAT others(13): Show |
A | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2975+427_2975+446d others(22): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923907 | |||||
| chrX:105923921
|
ATATATG | A | 11 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(8): Show | 11 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2975+441_2975+446d others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923921 | |||||
| chrX:105923923
|
ATATG | A | 11 | a0002c0002t0002g0205a0003c0003t0003g0013a0003c0003t0003g0023others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.2975+443_2975+446d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923923 | |||||
| chrX:105923925
|
ATG | A | 13 | a0003c0003t0003g0010a0003c0003t0003g0012a0003c0003t0003g0024others(10): Show | 13 | HG02451.hp1 HG02559.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.2975+446_2975+447d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923925 | |||||
| chrX:105923926
|
T | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0164 | 2 | NA18982.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2975+444T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | chrX | 105923926 | ||||||
| chrX:105923927
|
G | A | 46 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(43): Show | 47 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.2975+445G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | chrX | 105923927 | ||||||
| chrX:105924169
|
AT | A | 1 | a0008c0013t0001g0041 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2976-525delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | chrX | 105924169 | ||||||
| chrX:105924427
|
C | CTT | 1 | a0001c0001t0001g0178 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2976-267_2976-266i others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105924427 | |||||
| chrX:105924485
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2976-210G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | chrX | 105924485 | ||||||
| chrX:105924541
|
G | T | 86 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(83): Show | 87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.2976-154G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | chrX | 105924541 | ||||||
| chrX:105924602
|
G | T | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.2976-93G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | chrX | 105924602 | ||||||
| chrX:105925566
|
G | T | 1 | a0002c0002t0005g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3312+535G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105925566 | ||||||
| chrX:105925664
|
AT | A | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3312+639delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chrX | 105925664 | |||||
| chrX:105926068
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0172 | 3 | HG00609.hp1 NA18944.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.3312+1037C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105926068 | ||||||
| chrX:105926069
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.3312+1038G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105926069 | ||||||
| chrX:105926202
|
G | A | 45 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(42): Show | 46 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.3312+1171G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105926202 | ||||||
| chrX:105926378
|
T | C | 2 | a0002c0002t0005g0210a0002c0002t0005g0211 | 2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3312+1347T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105926378 | ||||||
| chrX:105926418
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3312+1387C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105926418 | ||||||
| chrX:105927398
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3312+2367A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105927398 | ||||||
| chrX:105927674
|
T | C | 1 | a0002c0002t0002g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3312+2643T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105927674 | ||||||
| chrX:105927710
|
C | CT | 1 | a0008c0013t0001g0041 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3312+2686dupT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chrX | 105927710 | |||||
| chrX:105927786
|
A | T | 44 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(41): Show | 45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.3312+2755A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105927786 | ||||||
| chrX:105928532
|
G | T | 1 | a0001c0001t0007g0119 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3312+3501G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105928532 | ||||||
| chrX:105928852
|
T | C | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3312+3821T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105928852 | ||||||
| chrX:105928858
|
T | A | 1 | a0003c0003t0003g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3312+3827T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105928858 | ||||||
| chrX:105929394
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3312+4363A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105929394 | ||||||
| chrX:105929542
|
CTG | C | 21 | a0003c0003t0003g0012a0003c0003t0003g0013a0003c0003t0003g0023others(18): Show | 21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.3312+4513_3312+451 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chrX | 105929542 | |||||
| chrX:105929552
|
G | A | 1 | a0005c0007t0003g0017 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3312+4521G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105929552 | ||||||
| chrX:105929764
|
G | C | 1 | a0002c0002t0002g0045 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3313-4494G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105929764 | ||||||
| chrX:105929850
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3313-4408G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105929850 | ||||||
| chrX:105930041
|
G | A | 86 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(83): Show | 87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.3313-4217G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105930041 | ||||||
| chrX:105930105
|
A | G | 1 | a0009c0014t0001g0135 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3313-4153A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105930105 | ||||||
| chrX:105930117
|
C | T | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.3313-4141C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105930117 | ||||||
| chrX:105930258
|
C | CT | 1 | a0002c0002t0011g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3313-3991dupT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chrX | 105930258 | |||||
| chrX:105930447
|
G | T | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3313-3811G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105930447 | ||||||
| chrX:105930896
|
C | T | 1 | a0003c0003t0003g0028 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3313-3362C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105930896 | ||||||
| chrX:105930900
|
G | T | 1 | a0002c0009t0005g0209 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3313-3358G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105930900 | ||||||
| chrX:105930985
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3313-3273C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105930985 | ||||||
| chrX:105931076
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(209): Show | 217 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(214): Show |
intron_variant | MODIFIER | c.3313-3182T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105931076 | ||||||
| chrX:105931404
|
A | G | 5 | a0003c0003t0003g0036a0003c0003t0003g0038a0003c0003t0003g0039others(2): Show | 5 | HG01884.hp2 HG02622.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.3313-2854A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105931404 | ||||||
| chrX:105931425
|
G | A | 1 | a0004c0004t0003g0014 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3313-2833G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105931425 | ||||||
| chrX:105931562
|
G | A | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.3313-2696G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105931562 | ||||||
| chrX:105931721
|
G | T | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3313-2537G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105931721 | ||||||
| chrX:105933166
|
G | GTCTA | 37 | a0001c0001t0001g0106a0001c0001t0001g0152a0001c0001t0001g0156others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.3313-1044_3313-104 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chrX | 105933166 | |||||
| chrX:105933166
|
G | GTCTATCT others(1): Show |
3 | a0001c0001t0004g0186a0002c0002t0002g0059a0002c0002t0005g0199 | 3 | HG01192.hp1 NA18906.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.3313-1048_3313-104 others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chrX | 105933166 | |||||
| chrX:105933166
|
GTCTA | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0001g0091others(85): Show | 90 | HG00642.hp1 HG00673.hp1 HG00733.hp2 others(87): Show |
intron_variant | MODIFIER | c.3313-1044_3313-104 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chrX | 105933166 | |||||
| chrX:105933166
|
GTCTATCT others(1): Show |
G | 5 | a0001c0001t0001g0087a0001c0001t0001g0120a0001c0001t0001g0138others(2): Show | 5 | HG02056.hp1 NA18982.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.3313-1048_3313-104 others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chrX | 105933166 | |||||
| chrX:105933166
|
GTCTATCT others(5): Show |
G | 2 | a0001c0001t0001g0109a0001c0001t0001g0124 | 2 | HG02523.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.3313-1052_3313-104 others(16): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chrX | 105933166 | |||||
| chrX:105933166
|
GTCTATCT others(13): Show |
G | 1 | a0001c0005t0001g0004 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3313-1060_3313-104 others(24): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chrX | 105933166 | |||||
| chrX:105933333
|
AT | A | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3313-921delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chrX | 105933333 | |||||
| chrX:105933344
|
AAAAGGAC others(1): Show |
A | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3313-913_3313-906d others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105933344 | ||||||
| chrX:105933486
|
A | G | 1 | a0002c0002t0005g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3313-772A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105933486 | ||||||
| chrX:105933824
|
T | C | 82 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(79): Show | 83 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.3313-434T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105933824 | ||||||
| chrX:105934729
|
C | T | 8 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0190others(5): Show | 8 | HG00140.hp1 HG00280.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.3499+285C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 20/28 | chrX | 105934729 | ||||||
| chrX:105934841
|
C | T | 3 | a0002c0002t0002g0060a0002c0002t0002g0061a0002c0002t0002g0062 | 3 | HG02486.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3500-329C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 20/28 | chrX | 105934841 | ||||||
| chrX:105934865
|
C | T | 1 | a0001c0001t0004g0195 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3500-305C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 20/28 | chrX | 105934865 | ||||||
| chrX:105934997
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3500-173C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 20/28 | chrX | 105934997 | ||||||
| chrX:105935140
|
C | T | 109 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0090others(106): Show | 110 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(107): Show |
intron_variant | MODIFIER | c.3500-30C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 20/28 | chrX | 105935140 | ||||||
| chrX:105935418
|
C | A | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.3655+93C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105935418 | ||||||
| chrX:105935513
|
C | T | 1 | a0003c0003t0003g0009 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3655+188C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105935513 | ||||||
| chrX:105935567
|
G | A | 41 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(38): Show | 42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.3655+242G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105935567 | ||||||
| chrX:105935770
|
G | A | 1 | a0002c0002t0002g0048 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3655+445G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105935770 | ||||||
| chrX:105935790
|
A | C | 1 | a0007c0010t0005g0088 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3655+465A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105935790 | ||||||
| chrX:105935813
|
T | TTA | 3 | a0001c0001t0001g0133a0001c0001t0004g0090a0002c0002t0005g0203 | 3 | HG00733.hp2 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3655+505_3655+506d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chrX | 105935813 | |||||
| chrX:105935813
|
TTA | T | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.3655+505_3655+506d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chrX | 105935813 | |||||
| chrX:105935831
|
A | G | 1 | a0003c0003t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3655+506A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105935831 | ||||||
| chrX:105936179
|
T | C | 1 | a0002c0002t0002g0050 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3655+854T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105936179 | ||||||
| chrX:105936386
|
C | A | 1 | a0001c0001t0004g0196 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3656-1053C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105936386 | ||||||
| chrX:105936435
|
A | G | 4 | a0001c0001t0001g0093a0001c0001t0001g0101a0001c0001t0001g0136others(1): Show | 4 | HG02080.hp2 HG02083.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.3656-1004A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105936435 | ||||||
| chrX:105936509
|
A | G | 45 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(42): Show | 46 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.3656-930A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105936509 | ||||||
| chrX:105936711
|
C | A | 1 | a0001c0001t0001g0189 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3656-728C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105936711 | ||||||
| chrX:105936719
|
T | G | 1 | a0001c0001t0001g0169 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3656-720T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105936719 | ||||||
| chrX:105936976
|
C | T | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.3656-463C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105936976 | ||||||
| chrX:105937306
|
T | A | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3656-133T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105937306 | ||||||
| chrX:105937915
|
G | A | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3799+333G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105937915 | ||||||
| chrX:105938154
|
G | A | 1 | a0002c0002t0011g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3799+572G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105938154 | ||||||
| chrX:105938207
|
A | G | 9 | a0001c0001t0001g0100a0001c0001t0001g0120a0001c0001t0001g0126others(6): Show | 9 | HG01978.hp2 NA18939.hp2 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.3799+625A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105938207 | ||||||
| chrX:105938236
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(209): Show | 217 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(214): Show |
intron_variant | MODIFIER | c.3799+654A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105938236 | ||||||
| chrX:105938515
|
A | C | 1 | a0001c0001t0001g0185 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3799+933A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105938515 | ||||||
| chrX:105938608
|
C | G | 1 | a0003c0003t0003g0213 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3799+1026C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105938608 | ||||||
| chrX:105938668
|
C | T | 21 | a0003c0003t0003g0012a0003c0003t0003g0013a0003c0003t0003g0023others(18): Show | 21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.3799+1086C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105938668 | ||||||
| chrX:105939005
|
TG | T | 4 | a0003c0003t0003g0012a0003c0003t0003g0025a0003c0003t0003g0212others(1): Show | 4 | HG02451.hp1 HG02886.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3800-868delG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105939005 | ||||||
| chrX:105939007
|
A | T | 4 | a0003c0003t0003g0012a0003c0003t0003g0025a0003c0003t0003g0212others(1): Show | 4 | HG02451.hp1 HG02886.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3800-867A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105939007 | ||||||
| chrX:105939008
|
A | T | 4 | a0003c0003t0003g0012a0003c0003t0003g0025a0003c0003t0003g0212others(1): Show | 4 | HG02451.hp1 HG02886.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3800-866A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105939008 | ||||||
| chrX:105939009
|
A | T | 4 | a0003c0003t0003g0012a0003c0003t0003g0025a0003c0003t0003g0212others(1): Show | 4 | HG02451.hp1 HG02886.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3800-865A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105939009 | ||||||
| chrX:105939010
|
G | T | 4 | a0003c0003t0003g0012a0003c0003t0003g0025a0003c0003t0003g0212others(1): Show | 4 | HG02451.hp1 HG02886.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3800-864G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105939010 | ||||||
| chrX:105939012
|
A | T | 4 | a0003c0003t0003g0012a0003c0003t0003g0025a0003c0003t0003g0212others(1): Show | 4 | HG02451.hp1 HG02886.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3800-862A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105939012 | ||||||
| chrX:105939621
|
A | C | 1 | a0001c0001t0001g0113 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3800-253A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105939621 | ||||||
| chrX:105939685
|
G | A | 1 | a0003c0003t0003g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3800-189G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105939685 | ||||||
| chrX:105939769
|
G | A | 17 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(14): Show | 17 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.3800-105G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105939769 | ||||||
| chrX:105940371
|
A | AT | 1 | a0011c0006t0001g0117 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3958+348dupT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105940371 | |||||
| chrX:105940477
|
T | A | 44 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(41): Show | 45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.3958+445T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105940477 | ||||||
| chrX:105940519
|
T | C | 1 | a0002c0002t0011g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3958+487T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105940519 | ||||||
| chrX:105940764
|
A | G | 82 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(79): Show | 83 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.3958+732A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105940764 | ||||||
| chrX:105940862
|
A | G | 1 | a0002c0002t0002g0066 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3958+830A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105940862 | ||||||
| chrX:105941551
|
C | CAG | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3958+1521_3958+152 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941551 | |||||
| chrX:105941555
|
A | AAG | 19 | a0001c0001t0001g0110a0001c0001t0001g0152a0001c0001t0001g0184others(16): Show | 19 | HG00140.hp1 HG00673.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.3958+1559_3958+156 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | |||||
| chrX:105941555
|
A | AAGAG | 39 | a0001c0001t0001g0001a0001c0001t0001g0078a0001c0001t0001g0080others(36): Show | 41 | HG00642.hp1 HG01106.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.3958+1557_3958+156 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | |||||
| chrX:105941555
|
A | AAGAGAG | 23 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0095others(20): Show | 23 | HG01069.hp1 HG01071.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.3958+1555_3958+156 others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | |||||
| chrX:105941555
|
A | AAGAGAGA others(1): Show |
7 | a0001c0001t0001g0081a0001c0001t0001g0159a0002c0002t0002g0056others(4): Show | 7 | HG00621.hp1 HG01884.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3958+1553_3958+156 others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | |||||
| chrX:105941555
|
A | AAGAGAGA others(3): Show |
3 | a0003c0003t0003g0023a0003c0003t0003g0028a0003c0003t0003g0034 | 3 | HG01109.hp1 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3958+1551_3958+156 others(14): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | |||||
| chrX:105941555
|
A | AAGAGAGA others(5): Show |
3 | a0003c0003t0003g0013a0003c0003t0003g0024a0003c0003t0003g0029 | 3 | HG02922.hp2 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3958+1549_3958+156 others(16): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | |||||
| chrX:105941555
|
A | AAGAGAGA others(7): Show |
3 | a0003c0003t0003g0026a0003c0003t0003g0039a0003c0003t0003g0040 | 3 | HG02895.hp1 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3958+1547_3958+156 others(18): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | |||||
| chrX:105941555
|
A | AGAGAG | 3 | a0001c0001t0001g0098a0001c0001t0001g0108a0004c0004t0003g0018 | 3 | HG02145.hp1 NA18977.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.3958+1523_3958+152 others(9): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105941555 | ||||||
| chrX:105941555
|
A | AGAGAGAG | 1 | a0001c0001t0001g0182 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3958+1523_3958+152 others(11): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105941555 | ||||||
| chrX:105941555
|
A | AGAGAGAG others(8): Show |
1 | a0003c0011t0003g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3958+1523_3958+152 others(19): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105941555 | ||||||
| chrX:105941555
|
A | G | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3958+1523A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105941555 | ||||||
| chrX:105941555
|
AAG | A | 4 | a0001c0001t0004g0197a0001c0001t0004g0198a0001c0001t0007g0119others(1): Show | 4 | HG01891.hp1 HG02630.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3958+1559_3958+156 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | |||||
| chrX:105941555
|
AAGAG | A | 4 | a0001c0001t0001g0087a0002c0002t0002g0003a0002c0002t0002g0077others(1): Show | 4 | HG00741.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.3958+1557_3958+156 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | |||||
| chrX:105941555
|
AAGAGAGA others(1): Show |
A | 3 | a0002c0002t0005g0199a0002c0002t0005g0202a0002c0002t0011g0201 | 3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.3958+1553_3958+156 others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | |||||
| chrX:105941592
|
A | AGAGAGAG others(2): Show |
1 | a0001c0001t0001g0204 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3958+1560_3958+156 others(13): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105941592 | ||||||
| chrX:105942258
|
A | G | 2 | a0002c0002t0005g0210a0002c0002t0005g0211 | 2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3959-1683A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105942258 | ||||||
| chrX:105942278
|
A | G | 1 | a0002c0002t0002g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3959-1663A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105942278 | ||||||
| chrX:105942624
|
C | CT | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3959-1310dupT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105942624 | |||||
| chrX:105942793
|
A | AT | 1 | a0002c0002t0002g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3959-1137dupT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105942793 | |||||
| chrX:105942824
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3959-1117C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105942824 | ||||||
| chrX:105942888
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3959-1053G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105942888 | ||||||
| chrX:105943070
|
T | C | 1 | a0003c0003t0003g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3959-871T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105943070 | ||||||
| chrX:105943097
|
G | A | 1 | a0002c0002t0005g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3959-844G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105943097 | ||||||
| chrX:105943165
|
T | C | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.3959-776T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105943165 | ||||||
| chrX:105943260
|
C | T | 1 | a0002c0002t0005g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3959-681C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105943260 | ||||||
| chrX:105943316
|
A | G | 1 | a0002c0002t0002g0205 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3959-625A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105943316 | ||||||
| chrX:105943913
|
G | A | 1 | a0002c0002t0002g0057 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3959-28G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105943913 | ||||||
| chrX:105944251
|
T | C | 1 | a0008c0013t0001g0041 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4059+210T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105944251 | ||||||
| chrX:105944252
|
G | GT | 1 | a0008c0013t0001g0041 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4059+211_4059+212i others(3): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105944252 | ||||||
| chrX:105944456
|
T | C | 90 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(87): Show | 91 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.4059+415T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105944456 | ||||||
| chrX:105944474
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0124a0001c0001t0001g0138 | 3 | HG02056.hp1 HG02523.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.4059+433C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105944474 | ||||||
| chrX:105944476
|
AG | A | 1 | a0008c0013t0001g0041 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4059+438delG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chrX | 105944476 | |||||
| chrX:105944554
|
C | T | 1 | a0002c0002t0002g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4059+513C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105944554 | ||||||
| chrX:105944704
|
G | A | 41 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(38): Show | 42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.4059+663G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105944704 | ||||||
| chrX:105944801
|
G | A | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.4059+760G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105944801 | ||||||
| chrX:105944832
|
T | A | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.4059+791T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105944832 | ||||||
| chrX:105945149
|
C | G | 1 | a0002c0002t0005g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4060-723C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105945149 | ||||||
| chrX:105945223
|
G | T | 1 | a0001c0001t0001g0160 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.4060-649G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105945223 | ||||||
| chrX:105945241
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4060-631A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105945241 | ||||||
| chrX:105945332
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4060-540G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105945332 | ||||||
| chrX:105945584
|
G | A | 1 | a0002c0002t0002g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4060-288G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105945584 | ||||||
| chrX:105946208
|
A | G | 3 | a0002c0002t0002g0060a0002c0002t0002g0061a0002c0002t0002g0062 | 3 | HG02486.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4204-107A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 25/28 | chrX | 105946208 | ||||||
| chrX:105946816
|
A | C | 1 | a0002c0002t0011g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4353+352A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105946816 | ||||||
| chrX:105946864
|
T | C | 1 | a0002c0002t0011g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4353+400T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105946864 | ||||||
| chrX:105947061
|
A | G | 3 | a0002c0002t0005g0102a0002c0002t0012g0103a0007c0010t0005g0088 | 3 | HG02717.hp1 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4353+597A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105947061 | ||||||
| chrX:105947093
|
T | C | 2 | a0001c0001t0004g0092a0001c0001t0004g0132 | 2 | HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.4353+629T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105947093 | ||||||
| chrX:105947164
|
TGAAATAC others(296): Show |
T | 86 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(83): Show | 87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.4353+717_4353+1019 others(3): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chrX | 105947164 | |||||
| chrX:105947442
|
C | CA | 6 | a0001c0001t0001g0084a0001c0001t0001g0107a0001c0001t0001g0114others(3): Show | 6 | HG03492.hp1 HG03927.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.4353+999dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chrX | 105947442 | |||||
| chrX:105947442
|
C | CAA | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4353+998_4353+999d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chrX | 105947442 | |||||
| chrX:105947442
|
CA | C | 6 | a0001c0001t0001g0083a0001c0001t0001g0121a0001c0001t0001g0158others(3): Show | 6 | HG01069.hp1 HG01168.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.4353+999delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chrX | 105947442 | |||||
| chrX:105947642
|
A | T | 8 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0190others(5): Show | 8 | HG00140.hp1 HG00280.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.4353+1178A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105947642 | ||||||
| chrX:105947911
|
TACTC | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0006g0173 | 3 | HG01069.hp1 HG01071.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.4353+1449_4353+145 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chrX | 105947911 | |||||
| chrX:105948076
|
CT | C | 2 | a0008c0013t0001g0041a0010c0015t0010g0176 | 2 | HG02897.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.4354-1489delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chrX | 105948076 | |||||
| chrX:105948364
|
G | A | 1 | a0002c0002t0002g0053 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4354-1211G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105948364 | ||||||
| chrX:105948617
|
T | A | 1 | a0001c0001t0001g0109 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.4354-958T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105948617 | ||||||
| chrX:105948748
|
A | G | 4 | a0003c0003t0003g0024a0003c0003t0003g0028a0003c0003t0003g0029others(1): Show | 4 | HG02723.hp2 HG02965.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.4354-827A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105948748 | ||||||
| chrX:105948777
|
CT | C | 41 | a0001c0001t0001g0083a0001c0001t0001g0158a0001c0001t0004g0085others(38): Show | 41 | HG01069.hp1 HG01109.hp1 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.4354-784delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chrX | 105948777 | |||||
| chrX:105948840
|
A | T | 1 | a0001c0001t0001g0123 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.4354-735A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105948840 | ||||||
| chrX:105948985
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0099a0001c0001t0001g0106others(3): Show | 7 | HG00609.hp1 HG02135.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.4354-590G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105948985 | ||||||
| chrX:105949246
|
A | G | 41 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(38): Show | 42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.4354-329A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105949246 | ||||||
| chrX:105949919
|
G | A | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.4513+185G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105949919 | ||||||
| chrX:105950191
|
G | C | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.4513+457G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105950191 | ||||||
| chrX:105950244
|
G | A | 1 | a0005c0007t0003g0017 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4513+510G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105950244 | ||||||
| chrX:105950438
|
A | AAT | 1 | a0001c0001t0001g0078 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4513+709_4513+710d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950438 | |||||
| chrX:105950527
|
A | AGT | 17 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0083others(14): Show | 17 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.4513+843_4513+844d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | |||||
| chrX:105950527
|
A | AGTGT | 8 | a0001c0001t0001g0001a0001c0001t0001g0108a0001c0001t0001g0127others(5): Show | 10 | HG00642.hp1 HG01256.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.4513+841_4513+844d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | |||||
| chrX:105950527
|
A | AGTGTGT | 3 | a0001c0001t0001g0130a0001c0001t0001g0169a0002c0002t0002g0045 | 3 | HG01928.hp1 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.4513+839_4513+844d others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | |||||
| chrX:105950527
|
A | AGTGTGTG others(1): Show |
1 | a0001c0001t0001g0078 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4513+837_4513+844d others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | |||||
| chrX:105950527
|
AGT | A | 21 | a0001c0001t0001g0098a0001c0001t0001g0110a0001c0001t0001g0118others(18): Show | 21 | HG00735.hp1 HG01071.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.4513+843_4513+844d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | |||||
| chrX:105950527
|
AGTGT | A | 74 | a0001c0001t0001g0005a0001c0001t0001g0084a0001c0001t0001g0087others(71): Show | 75 | HG00140.hp1 HG00609.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.4513+841_4513+844d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | |||||
| chrX:105950527
|
AGTGTGT | A | 23 | a0001c0001t0001g0093a0001c0001t0001g0101a0001c0001t0001g0107others(20): Show | 24 | HG00280.hp1 HG01167.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.4513+839_4513+844d others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | |||||
| chrX:105950527
|
AGTGTGTG others(1): Show |
A | 8 | a0001c0001t0001g0100a0001c0001t0001g0128a0001c0001t0001g0151others(5): Show | 8 | HG03209.hp1 HG03453.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.4513+837_4513+844d others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | |||||
| chrX:105950527
|
AGTGTGTG others(3): Show |
A | 2 | a0001c0001t0001g0139a0001c0001t0001g0185 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4513+835_4513+844d others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | |||||
| chrX:105950527
|
AGTGTGTG others(11): Show |
A | 1 | a0003c0003t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4513+827_4513+844d others(20): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | |||||
| chrX:105950527
|
AGTGTGTG others(13): Show |
A | 21 | a0003c0003t0003g0010a0003c0003t0003g0012a0003c0003t0003g0013others(18): Show | 21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.4513+825_4513+844d others(22): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | |||||
| chrX:105950578
|
G | GT | 1 | a0002c0002t0002g0071 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4513+844_4513+845i others(3): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105950578 | ||||||
| chrX:105950614
|
A | G | 86 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0043others(83): Show | 87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.4513+880A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105950614 | ||||||
| chrX:105950823
|
C | CAG | 19 | a0002c0002t0005g0199a0002c0002t0005g0202a0002c0002t0011g0201others(16): Show | 19 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.4513+1113_4513+111 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950823 | |||||
| chrX:105951010
|
C | CT | 1 | a0001c0001t0004g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4513+1289dupT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105951010 | |||||
| chrX:105951281
|
T | C | 1 | a0002c0002t0002g0075 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4513+1547T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105951281 | ||||||
| chrX:105951477
|
G | A | 21 | a0003c0003t0003g0012a0003c0003t0003g0013a0003c0003t0003g0023others(18): Show | 21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.4514-1557G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105951477 | ||||||
| chrX:105951508
|
A | G | 1 | a0002c0002t0002g0054 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4514-1526A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105951508 | ||||||
| chrX:105952057
|
C | T | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.4514-977C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105952057 | ||||||
| chrX:105952115
|
G | T | 3 | a0002c0002t0005g0199a0002c0002t0005g0202a0002c0002t0011g0201 | 3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.4514-919G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105952115 | ||||||
| chrX:105952451
|
A | C | 1 | a0002c0002t0005g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4514-583A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105952451 | ||||||
| chrX:105952755
|
C | T | 3 | a0002c0002t0005g0199a0002c0002t0005g0202a0002c0002t0011g0201 | 3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.4514-279C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105952755 | ||||||
| chrX:105952763
|
A | G | 3 | a0002c0002t0002g0060a0002c0002t0002g0061a0002c0002t0002g0062 | 3 | HG02486.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4514-271A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105952763 | ||||||
| chrX:105953262
|
C | T | 1 | a0002c0009t0005g0209 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4653+89C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105953262 | ||||||
| chrX:105953549
|
C | T | 1 | a0010c0015t0010g0176 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.4653+376C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105953549 | ||||||
| chrX:105953755
|
C | T | 3 | a0002c0002t0005g0199a0002c0002t0005g0202a0002c0002t0011g0201 | 3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.4653+582C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105953755 | ||||||
| chrX:105953993
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4653+820G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105953993 | ||||||
| chrX:105954007
|
A | C | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.4653+834A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105954007 | ||||||
| chrX:105954086
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4653+913T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105954086 | ||||||
| chrX:105954203
|
A | G | 5 | a0001c0001t0001g0081a0001c0001t0001g0121a0001c0001t0001g0134others(2): Show | 5 | HG00621.hp1 NA18966.hp1 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.4653+1030A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105954203 | ||||||
| chrX:105954388
|
C | T | 2 | a0003c0003t0003g0011a0003c0003t0003g0019 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4654-1117C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105954388 | ||||||
| chrX:105954439
|
TA | T | 2 | a0003c0003t0003g0011a0003c0003t0003g0019 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4654-1062delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chrX | 105954439 | |||||
| chrX:105954530
|
A | G | 37 | a0003c0003t0003g0006a0003c0003t0003g0007a0003c0003t0003g0008others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.4654-975A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105954530 | ||||||
| chrX:105955236
|
CA | C | 1 | a0001c0001t0004g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4654-266delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chrX | 105955236 | |||||
| chrX:105955435
|
A | G | 4 | a0002c0002t0005g0208a0002c0002t0005g0210a0002c0002t0005g0211others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.4654-70A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105955435 |