Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 416 |
|---|---|
| ensemblid | ENSG00000062096.15 |
| hgncid | 721 |
| symbol | ARSF |
| name | arylsulfatase F |
| refseq_nuc | NM_001201539.2 |
| refseq_prot | NP_001188468.1 |
| ensembl_nuc | ENST00000381127.6 |
| ensembl_prot | ENSP00000370519.1 |
| mane_status | MANE Select |
| chr | chrX |
| start | 3041471 |
| end | 3112727 |
| strand | + |
| ver | v1.2 |
| region | chrX:3041471-3112727 |
| region5000 | chrX:3036471-3117727 |
| regionname0 | ARSF_chrX_3041471_3112727 |
| regionname5000 | ARSF_chrX_3036471_3117727 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000 | 0/0 | 0 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001 | 1/1 | 590 | 169 | 32 | 25 | 74 | 10 | 26 | 60 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0002 | 0/0 | 590 | 9 | 2 | 5 | 1 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0003 | 0/0 | 590 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0004 | 0/0 | 590 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0005 | 0/0 | 590 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0006 | 0/0 | 590 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0007 | 0/0 | 590 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0008 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1773 | 140 | 18 | 21 | 73 | 8 | 20 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0002 | 1/1 | 1773 | 15 | 4 | 4 | 1 | 2 | 2 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0003 | 0/0 | 1773 | 5 | 1 | 3 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0004 | 0/0 | 1773 | 4 | 1 | 2 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0005 | 0/0 | 1773 | 4 | 4 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0006 | 0/0 | 1773 | 3 | 1 | 2 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0007 | 0/0 | 1773 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0008 | 0/0 | 1773 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0009 | 0/0 | 1823 | 2 | 0 | 0 | 0 | 0 | 2 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0010 | 0/0 | 1773 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0011 | 0/0 | 1773 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0012 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0013 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0014 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0015 | 0/0 | 1773 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0016 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0017 | 0/0 | 1773 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0018 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0019 | 0/0 | 1775 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0020 | 0/0 | 1773 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0021 | 0/0 | 1773 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0022 | 0/0 | 1773 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| c0023 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 393 | 185 | 39 | 33 | 75 | 11 | 25 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| t0002 | 0/0 | 364 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| t0003 | 0/0 | 393 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| t0004 | 0/0 | 396 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| t0005 | 0/0 | 393 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| t0006 | 0/0 | 393 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| t0007 | 0/0 | 443 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0020 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0026 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0014 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0000c0018 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0001 | 0/0 | 1773 | 140 | 18 | 21 | 73 | 8 | 20 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0002 | 1/1 | 1773 | 15 | 4 | 4 | 1 | 2 | 2 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0005 | 0/0 | 1773 | 4 | 4 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0007 | 0/0 | 1773 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0009 | 0/0 | 1823 | 2 | 0 | 0 | 0 | 0 | 2 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0010 | 0/0 | 1773 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0012 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0015 | 0/0 | 1773 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0016 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0020 | 0/0 | 1773 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0002c0003 | 0/0 | 1773 | 5 | 1 | 3 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0002c0004 | 0/0 | 1773 | 4 | 1 | 2 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0003c0008 | 0/0 | 1773 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0003c0013 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0003c0017 | 0/0 | 1773 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0004c0011 | 0/0 | 1773 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0004c0023 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0005c0006 | 0/0 | 1773 | 3 | 1 | 2 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0006c0022 | 0/0 | 1773 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0007c0021 | 0/0 | 1773 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0008c0019 | 0/0 | 1775 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0014t0002 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0000c0018t0002 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0001t0001 | 0/0 | 2165 | 137 | 18 | 21 | 70 | 8 | 20 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0001t0004 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0001t0005 | 0/0 | 2165 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0001t0006 | 0/0 | 2165 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0002t0001 | 1/1 | 2165 | 15 | 4 | 4 | 1 | 2 | 2 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0005t0001 | 0/0 | 2165 | 4 | 4 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0007t0003 | 0/0 | 2165 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0009t0001 | 0/0 | 2215 | 2 | 0 | 0 | 0 | 0 | 2 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0010t0001 | 0/0 | 2165 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0012t0001 | 0/0 | 2165 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0015t0007 | 0/0 | 2215 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0016t0001 | 0/0 | 2165 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0001c0020t0001 | 0/0 | 2165 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0002c0003t0001 | 0/0 | 2165 | 5 | 1 | 3 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0002c0004t0001 | 0/0 | 2165 | 4 | 1 | 2 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0003c0008t0001 | 0/0 | 2165 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0003c0013t0001 | 0/0 | 2165 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0003c0017t0001 | 0/0 | 2165 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0004c0011t0001 | 0/0 | 2165 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0004c0023t0001 | 0/0 | 2165 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0005c0006t0001 | 0/0 | 2165 | 3 | 1 | 2 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0006c0022t0001 | 0/0 | 2165 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0007c0021t0001 | 0/0 | 2165 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| a0008c0019t0001 | 0/0 | 2167 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | copy fasta | chrX | 3036471 | 3117727 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0014t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0000c0018t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0002t0001g0020 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0002t0001g0026 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0005t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0005t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0005t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0005t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0007t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0007t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0009t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0009t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0010t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0010t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0012t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0015t0007g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0016t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0001c0020t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0002c0003t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0002c0003t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0002c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0002c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0002c0003t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0002c0004t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0002c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0002c0004t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0002c0004t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0003c0008t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0003c0008t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0003c0013t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0003c0017t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0004c0011t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0004c0011t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0004c0023t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0005c0006t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0005c0006t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0005c0006t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0006c0022t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0007c0021t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| a0008c0019t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0023 | EUR | GBR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG00099 | hp2 | a0002 | c0004 | t0001 | g0127 | EUR | GBR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | GBR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | FIN | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0021 | EUR | FIN | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | FIN | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG00597 | hp1 | a0006 | c0022 | t0001 | g0174 | EAS | CHS | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG00673 | hp1 | a0007 | c0021 | t0001 | g0102 | EAS | CHS | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01070 | hp1 | a0002 | c0004 | t0001 | g0182 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01071 | hp2 | a0002 | c0004 | t0001 | g0181 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01074 | hp1 | a0003 | c0017 | t0001 | g0139 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0187 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01167 | hp1 | a0002 | c0003 | t0001 | g0010 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01168 | hp1 | a0005 | c0006 | t0001 | g0006 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01169 | hp1 | a0002 | c0003 | t0001 | g0012 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01169 | hp2 | a0005 | c0006 | t0001 | g0005 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01496 | hp2 | a0002 | c0003 | t0001 | g0146 | AMR | CLM | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | IBS | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01884 | hp1 | a0000 | c0014 | t0002 | g0022 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02083 | hp1 | a0002 | c0003 | t0001 | g0104 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02257 | hp2 | a0001 | c0007 | t0003 | g0028 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02258 | hp1 | a0003 | c0008 | t0001 | g0115 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02280 | hp1 | a0001 | c0010 | t0001 | g0030 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02280 | hp2 | a0001 | c0016 | t0001 | g0156 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0126 | AMR | PEL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02451 | hp2 | a0000 | c0018 | t0002 | g0129 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02572 | hp1 | a0004 | c0011 | t0001 | g0024 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02622 | hp1 | a0002 | c0004 | t0001 | g0087 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0186 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0013 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02735 | hp1 | a0001 | c0020 | t0001 | g0092 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02809 | hp1 | a0001 | c0010 | t0001 | g0037 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0185 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0184 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02922 | hp1 | a0001 | c0005 | t0001 | g0039 | AFR | ESN | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02965 | hp1 | a0001 | c0007 | t0003 | g0183 | AFR | ESN | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03041 | hp1 | a0001 | c0005 | t0001 | g0009 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03041 | hp2 | a0004 | c0023 | t0001 | g0169 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03098 | hp1 | a0001 | c0005 | t0001 | g0040 | AFR | MSL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03139 | hp1 | a0003 | c0008 | t0001 | g0167 | AFR | ESN | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03225 | hp1 | a0002 | c0003 | t0001 | g0047 | AFR | MSL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03239 | hp2 | a0001 | c0015 | t0007 | g0018 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03491 | hp1 | a0001 | c0009 | t0001 | g0014 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03492 | hp1 | a0001 | c0009 | t0001 | g0015 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0027 | SAS | STU | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0112 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19030 | hp1 | a0001 | c0012 | t0001 | g0086 | AFR | LWK | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19030 | hp2 | a0003 | c0013 | t0001 | g0096 | AFR | LWK | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19056 | hp1 | a0001 | c0001 | t0006 | g0064 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19076 | hp1 | a0008 | c0019 | t0001 | g0076 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | YRI | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA20129 | hp1 | a0004 | c0011 | t0001 | g0031 | AFR | ASW | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA20129 | hp2 | a0001 | c0005 | t0001 | g0007 | AFR | ASW | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | TSI | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA21309 | hp1 | a0005 | c0006 | t0001 | g0128 | AFR | LWK | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0026 | REF | REF | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0020 | REF | REF | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
| 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:3081002
|
C | T | 1 | a0004 | 3 | HG02572.hp1 HG03041.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.395C>T | p.Thr132Met | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/11 | 616/2165 | 395/1773 | 132/590 | chrX | 3081002 | ||
| chrX:3084428
|
A | T | 1 | a0006 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.592A>T | p.Ile198Phe | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/11 | 813/2165 | 592/1773 | 198/590 | chrX | 3084428 | ||
| chrX:3084434
|
A | G | 1 | a0005 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.598A>G | p.Ile200Val | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/11 | 819/2165 | 598/1773 | 200/590 | chrX | 3084434 | ||
| chrX:3084485
|
C | T | 1 | a0007 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.649C>T | p.Leu217Phe | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/11 | 870/2165 | 649/1773 | 217/590 | chrX | 3084485 | ||
| chrX:3101123
|
G | A | 1 | a0003 | 4 | HG01074.hp1 HG02258.hp1 HG03139.hp1 others(1): Show |
missense_variant | MODERATE | c.1004G>A | p.Arg335Lys | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/11 | 1225/2165 | 1004/1773 | 335/590 | chrX | 3101123 | ||
| chrX:3103777
|
G | A | 1 | a0006 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.1118G>A | p.Gly373Glu | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/11 | 1339/2165 | 1118/1773 | 373/590 | chrX | 3103777 | ||
| chrX:3112242
|
G | GT | 1 | a0008 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1460dupT | p.Thr488fs | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 1682/2165 | 1461/1773 | 487/590 | INFO_REALIGN_3_PRIME | chrX | 3112242 | |
| chrX:3112266
|
G | GA | 1 | a0008 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1483_1484insA | p.Gly495fs | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 1705/2165 | 1484/1773 | 495/590 | chrX | 3112266 | ||
| chrX:3112362
|
C | T | 2 | a0002a0006 | 10 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(7): Show |
missense_variant | MODERATE | c.1579C>T | p.His527Tyr | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 1800/2165 | 1579/1773 | 527/590 | chrX | 3112362 | ||
| chrX:3112392
|
GC | G | 1 | a0008 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1612delC | p.Leu538fs | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 1833/2165 | 1612/1773 | 538/590 | INFO_REALIGN_3_PRIME | chrX | 3112392 | |
| chrX:3112533
|
C | CG | 1 | a0008 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1754dupG | p.Pro586fs | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 1976/2165 | 1755/1773 | 585/590 | INFO_REALIGN_3_PRIME | chrX | 3112533 |
| 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:3084280
|
T | C | 1 | a0001c0012 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.444T>C | p.Ser148Ser | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/11 | 665/2165 | 444/1773 | 148/590 | chrX | 3084280 | ||
| chrX:3084472
|
C | A | 1 | a0003c0013 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.636C>A | p.Val212Val | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/11 | 857/2165 | 636/1773 | 212/590 | chrX | 3084472 | ||
| chrX:3084646
|
A | G | 15 | a0000c0018a0001c0001a0001c0005others(12): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
synonymous_variant | LOW | c.810A>G | p.Glu270Glu | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/11 | 1031/2165 | 810/1773 | 270/590 | chrX | 3084646 | ||
| chrX:3101106
|
C | T | 2 | a0001c0007a0001c0010 | 4 | HG02257.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
synonymous_variant | LOW | c.987C>T | p.Ile329Ile | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/11 | 1208/2165 | 987/1773 | 329/590 | chrX | 3101106 | ||
| chrX:3110219
|
C | T | 9 | a0001c0005a0001c0015a0001c0016others(6): Show | 15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
synonymous_variant | LOW | c.1357C>T | p.Leu453Leu | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/11 | 1578/2165 | 1357/1773 | 453/590 | chrX | 3110219 | ||
| chrX:3110248
|
C | T | 9 | a0001c0005a0001c0015a0001c0016others(6): Show | 15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
synonymous_variant | LOW | c.1386C>T | p.Asp462Asp | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/11 | 1607/2165 | 1386/1773 | 462/590 | chrX | 3110248 | ||
| chrX:3112385
|
G | A | 4 | a0001c0015a0001c0020a0003c0017others(1): Show | 6 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(3): Show |
synonymous_variant | LOW | c.1602G>A | p.Val534Val | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 1823/2165 | 1602/1773 | 534/590 | chrX | 3112385 |
| 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:3041506
|
G | GC | 1 | a0001c0001t0004 | 1 | NA19063.hp1 | 5_prime_UTR_variant | MODIFIER | c.-186_-185insC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/11 | 26594 | chrX | 3041506 | |||||
| chrX:3041558
|
T | TG | 1 | a0001c0001t0004 | 1 | NA19063.hp1 | 5_prime_UTR_variant | MODIFIER | c.-131dupG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/11 | 26539 | INFO_REALIGN_3_PRIME | chrX | 3041558 | ||||
| chrX:3041652
|
T | TG | 1 | a0001c0001t0004 | 1 | NA19063.hp1 | 5_prime_UTR_variant | MODIFIER | c.-40_-39insG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/11 | 26448 | chrX | 3041652 | |||||
| chrX:3112535
|
G | GGGTCCTA others(43): Show |
1 | a0001c0009t0001 | 2 | HG03491.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*18_*67dupGAGGAAGC others(42): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 68 | INFO_REALIGN_3_PRIME | chrX | 3112535 | ||||
| chrX:3112535
|
GGGTCCTA others(43): Show |
G | 2 | a0000c0014t0002a0000c0018t0002 | 2 | HG01884.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*18_*67delGAGGAAGC others(42): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 18 | INFO_REALIGN_3_PRIME | chrX | 3112535 | ||||
| chrX:3112574
|
G | GAGGAAGC others(43): Show |
1 | a0001c0015t0007 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*26_*75dupCTTTGGTC others(42): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 76 | INFO_REALIGN_3_PRIME | chrX | 3112574 | ||||
| chrX:3112594
|
C | A | 1 | a0001c0001t0005 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*38C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 38 | chrX | 3112594 | |||||
| chrX:3112654
|
T | G | 1 | a0001c0001t0006 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*98T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 98 | chrX | 3112654 | |||||
| chrX:3112719
|
G | T | 1 | a0001c0007t0003 | 2 | HG02257.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*163G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 163 | chrX | 3112719 |
| 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:3041820
|
C | T | 152 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(149): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+157C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3041820 | ||||||
| chrX:3042175
|
A | T | 3 | a0001c0001t0001g0041a0001c0005t0001g0039a0001c0005t0001g0040 | 3 | HG01884.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-29+512A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3042175 | ||||||
| chrX:3042193
|
A | AT | 1 | a0001c0001t0001g0189 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-29+535dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3042193 | |||||
| chrX:3042319
|
G | C | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-29+656G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3042319 | ||||||
| chrX:3042420
|
AAATTG | A | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-29+758_-29+762del others(5): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3042420 | ||||||
| chrX:3042440
|
T | G | 1 | a0001c0001t0001g0042 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-29+777T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3042440 | ||||||
| chrX:3042464
|
CA | C | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+804delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3042464 | |||||
| chrX:3042476
|
A | C | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+813A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3042476 | ||||||
| chrX:3042619
|
C | A | 1 | a0001c0001t0001g0043 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-29+956C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3042619 | ||||||
| chrX:3042880
|
C | T | 9 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(6): Show | 9 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+1217C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3042880 | ||||||
| chrX:3043070
|
G | GCC | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+1408_-29+1409i others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3043070 | |||||
| chrX:3043076
|
A | AC | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+1416dupC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3043076 | |||||
| chrX:3043143
|
A | AG | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+1481dupG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3043143 | |||||
| chrX:3043213
|
GA | G | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+1555delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3043213 | |||||
| chrX:3043277
|
A | C | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-29+1614A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3043277 | ||||||
| chrX:3043299
|
T | TC | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+1637dupC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3043299 | |||||
| chrX:3043337
|
CA | C | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+1681delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3043337 | |||||
| chrX:3043414
|
T | TA | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+1756dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3043414 | |||||
| chrX:3043564
|
C | T | 9 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(6): Show | 9 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+1901C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3043564 | ||||||
| chrX:3043584
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-29+1921C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3043584 | ||||||
| chrX:3043600
|
CT | C | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+1941delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3043600 | |||||
| chrX:3043610
|
G | C | 9 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(6): Show | 9 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+1947G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3043610 | ||||||
| chrX:3043658
|
T | C | 153 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(150): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-29+1995T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3043658 | ||||||
| chrX:3043693
|
AT | A | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+2035delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3043693 | |||||
| chrX:3043771
|
CTGTT | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 5 | HG00738.hp1 HG01256.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+2115_-29+2118d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3043771 | |||||
| chrX:3043792
|
T | TTTA | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+2130_-29+2131i others(5): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3043792 | |||||
| chrX:3043794
|
A | T | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+2131A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3043794 | ||||||
| chrX:3043851
|
G | T | 159 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(156): Show | 163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-29+2188G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3043851 | ||||||
| chrX:3043977
|
T | TG | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+2318dupG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3043977 | |||||
| chrX:3044009
|
A | AG | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+2347dupG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3044009 | |||||
| chrX:3044070
|
T | C | 171 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(168): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.-29+2407T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3044070 | ||||||
| chrX:3044178
|
A | G | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-29+2515A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3044178 | ||||||
| chrX:3044262
|
AT | A | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+2602delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3044262 | |||||
| chrX:3044416
|
T | C | 153 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(150): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-29+2753T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3044416 | ||||||
| chrX:3044444
|
T | C | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-29+2781T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3044444 | ||||||
| chrX:3044461
|
C | G | 1 | a0001c0001t0001g0180 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-29+2798C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3044461 | ||||||
| chrX:3044559
|
A | AC | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+2896_-29+2897i others(3): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3044559 | ||||||
| chrX:3044573
|
AGG | A | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+2913_-29+2914d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3044573 | |||||
| chrX:3044580
|
G | A | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-29+2917G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3044580 | ||||||
| chrX:3044665
|
A | C | 1 | a0001c0001t0001g0041 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-29+3002A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3044665 | ||||||
| chrX:3044666
|
T | A | 159 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(156): Show | 163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-29+3003T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3044666 | ||||||
| chrX:3044771
|
G | A | 12 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-29+3108G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3044771 | ||||||
| chrX:3044771
|
G | GT | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+3113dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3044771 | |||||
| chrX:3044948
|
T | TA | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+3288dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3044948 | |||||
| chrX:3045151
|
G | GA | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+3493dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3045151 | |||||
| chrX:3045180
|
C | CT | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+3520dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3045180 | |||||
| chrX:3045202
|
T | TG | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+3541dupG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3045202 | |||||
| chrX:3045236
|
TG | T | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+3577delG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3045236 | |||||
| chrX:3045359
|
C | CG | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+3700dupG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3045359 | |||||
| chrX:3045370
|
A | AC | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+3707_-29+3708i others(3): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3045370 | ||||||
| chrX:3045383
|
T | TG | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+3721dupG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3045383 | |||||
| chrX:3045391
|
T | TG | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+3729dupG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3045391 | |||||
| chrX:3045554
|
C | CT | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01978.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-29+3909dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3045554 | |||||
| chrX:3045554
|
C | CTT | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+3908_-29+3909d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3045554 | |||||
| chrX:3045554
|
CT | C | 14 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(11): Show | 14 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29+3909delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3045554 | |||||
| chrX:3045568
|
T | C | 1 | a0002c0003t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-29+3905T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3045568 | ||||||
| chrX:3045642
|
A | G | 151 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(148): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-29+3979A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3045642 | ||||||
| chrX:3045649
|
G | A | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-29+3986G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3045649 | ||||||
| chrX:3045712
|
C | T | 151 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(148): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-29+4049C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3045712 | ||||||
| chrX:3045713
|
A | G | 151 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(148): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-29+4050A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3045713 | ||||||
| chrX:3045715
|
CT | C | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+4053delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3045715 | ||||||
| chrX:3045716
|
T | C | 150 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(147): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-29+4053T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3045716 | ||||||
| chrX:3045853
|
GC | G | 4 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+4192delC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3045853 | |||||
| chrX:3045865
|
G | GT | 1 | a0001c0001t0001g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-29+4210dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3045865 | |||||
| chrX:3045869
|
TTTTTGTT others(2): Show |
T | 6 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0186others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+4215_-29+4223d others(11): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3045869 | |||||
| chrX:3045878
|
GT | G | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+4219delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3045878 | |||||
| chrX:3045930
|
T | TG | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+4271dupG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3045930 | |||||
| chrX:3045944
|
G | A | 151 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(148): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-29+4281G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3045944 | ||||||
| chrX:3046129
|
GC | G | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+4469delC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3046129 | |||||
| chrX:3046133
|
G | A | 151 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(148): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-29+4470G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3046133 | ||||||
| chrX:3046142
|
TC | T | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+4482delC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3046142 | |||||
| chrX:3046205
|
C | T | 4 | a0001c0002t0001g0011a0001c0002t0001g0025a0001c0002t0001g0026others(1): Show | 4 | HG00642.hp1 HG00735.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+4542C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3046205 | ||||||
| chrX:3046301
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-29+4638C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3046301 | ||||||
| chrX:3046419
|
T | TC | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+4757dupC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3046419 | |||||
| chrX:3046442
|
G | A | 2 | a0002c0004t0001g0181a0002c0004t0001g0182 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-29+4779G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3046442 | ||||||
| chrX:3046705
|
G | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG00323.hp2 HG01106.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-29+5042G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3046705 | ||||||
| chrX:3046802
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-29+5139A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3046802 | ||||||
| chrX:3047008
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0175 | 3 | NA18951.hp1 NA18994.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-29+5345A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047008 | ||||||
| chrX:3047041
|
A | G | 172 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(169): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-29+5378A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047041 | ||||||
| chrX:3047125
|
T | C | 164 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(161): Show | 168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.-29+5462T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047125 | ||||||
| chrX:3047183
|
AT | A | 11 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(8): Show | 11 | HG01069.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-29+5533delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3047183 | |||||
| chrX:3047476
|
A | AG | 152 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(149): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+5813_-29+5814i others(3): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047476 | ||||||
| chrX:3047481
|
T | G | 152 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(149): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+5818T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047481 | ||||||
| chrX:3047485
|
C | T | 152 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(149): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+5822C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047485 | ||||||
| chrX:3047773
|
C | T | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-29+6110C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047773 | ||||||
| chrX:3047840
|
G | A | 152 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(149): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+6177G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047840 | ||||||
| chrX:3047844
|
T | C | 152 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(149): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+6181T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047844 | ||||||
| chrX:3047892
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-29+6229C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047892 | ||||||
| chrX:3047905
|
T | C | 152 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(149): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+6242T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047905 | ||||||
| chrX:3047981
|
A | G | 153 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(150): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-29+6318A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047981 | ||||||
| chrX:3048180
|
C | T | 152 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(149): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+6517C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3048180 | ||||||
| chrX:3048208
|
T | A | 152 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(149): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+6545T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3048208 | ||||||
| chrX:3048376
|
G | A | 1 | a0004c0011t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-29+6713G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3048376 | ||||||
| chrX:3048417
|
G | A | 1 | a0004c0011t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-29+6754G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3048417 | ||||||
| chrX:3048441
|
T | C | 152 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(149): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+6778T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3048441 | ||||||
| chrX:3048745
|
A | G | 1 | a0004c0011t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-29+7082A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3048745 | ||||||
| chrX:3048900
|
C | T | 3 | a0001c0001t0001g0061a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG02135.hp1 NA18986.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-29+7237C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3048900 | ||||||
| chrX:3048965
|
T | A | 152 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(149): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+7302T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3048965 | ||||||
| chrX:3049015
|
A | G | 151 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(148): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-29+7352A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049015 | ||||||
| chrX:3049082
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-29+7419G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049082 | ||||||
| chrX:3049096
|
G | A | 179 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(176): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-29+7433G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049096 | ||||||
| chrX:3049135
|
A | G | 152 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(149): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+7472A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049135 | ||||||
| chrX:3049145
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-29+7482C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049145 | ||||||
| chrX:3049211
|
T | C | 5 | a0001c0001t0001g0032a0001c0001t0001g0038a0001c0010t0001g0030others(2): Show | 5 | HG02280.hp1 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29+7548T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049211 | ||||||
| chrX:3049331
|
C | T | 6 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0186others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+7668C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049331 | ||||||
| chrX:3049345
|
T | TG | 1 | a0001c0001t0001g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-29+7687dupG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3049345 | |||||
| chrX:3049397
|
A | T | 1 | a0004c0011t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-29+7734A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049397 | ||||||
| chrX:3049659
|
A | G | 152 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(149): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+7996A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049659 | ||||||
| chrX:3049864
|
AT | A | 1 | a0001c0001t0004g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+8206delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3049864 | |||||
| chrX:3049929
|
T | C | 161 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(158): Show | 165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-29+8266T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049929 | ||||||
| chrX:3050027
|
T | G | 1 | a0001c0001t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-29+8364T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050027 | ||||||
| chrX:3050069
|
G | C | 161 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(158): Show | 165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-29+8406G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050069 | ||||||
| chrX:3050143
|
T | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0062 | 2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-29+8480T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050143 | ||||||
| chrX:3050271
|
T | C | 8 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0186others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+8608T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050271 | ||||||
| chrX:3050391
|
G | A | 161 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(158): Show | 165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-29+8728G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050391 | ||||||
| chrX:3050407
|
G | A | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-29+8744G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050407 | ||||||
| chrX:3050546
|
C | CA | 24 | a0001c0001t0001g0044a0001c0001t0001g0063a0001c0001t0001g0066others(21): Show | 24 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.-29+8900dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3050546 | |||||
| chrX:3050546
|
C | CAA | 1 | a0001c0007t0003g0183 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-29+8899_-29+8900d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3050546 | |||||
| chrX:3050546
|
CA | C | 6 | a0001c0001t0001g0053a0001c0001t0001g0168a0001c0001t0001g0170others(3): Show | 6 | HG02602.hp1 HG03041.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+8900delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3050546 | |||||
| chrX:3050607
|
T | C | 161 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(158): Show | 165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-29+8944T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050607 | ||||||
| chrX:3050687
|
G | C | 8 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0186others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+9024G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050687 | ||||||
| chrX:3050874
|
G | T | 161 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(158): Show | 165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-29+9211G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050874 | ||||||
| chrX:3050902
|
C | T | 1 | a0001c0002t0001g0027 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-29+9239C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050902 | ||||||
| chrX:3050917
|
C | T | 151 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(148): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-29+9254C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050917 | ||||||
| chrX:3050979
|
C | T | 1 | a0004c0011t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-29+9316C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050979 | ||||||
| chrX:3051026
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-29+9363C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3051026 | ||||||
| chrX:3051194
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-29+9531C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3051194 | ||||||
| chrX:3051207
|
C | A | 1 | a0002c0003t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-29+9544C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3051207 | ||||||
| chrX:3051489
|
T | C | 9 | a0001c0001t0001g0043a0001c0001t0001g0078a0001c0001t0001g0079others(6): Show | 9 | HG02071.hp1 NA18612.hp1 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+9826T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3051489 | ||||||
| chrX:3051497
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-29+9834C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3051497 | ||||||
| chrX:3051498
|
G | A | 14 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(11): Show | 14 | HG01168.hp1 HG01169.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-29+9835G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3051498 | ||||||
| chrX:3051590
|
C | CTA | 23 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(20): Show | 23 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.-29+9928_-29+9929i others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3051590 | |||||
| chrX:3051883
|
C | T | 9 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0186others(6): Show | 9 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+10220C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3051883 | ||||||
| chrX:3051905
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-29+10242A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3051905 | ||||||
| chrX:3051995
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-29+10332A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3051995 | ||||||
| chrX:3052028
|
C | CA | 5 | a0001c0001t0001g0029a0001c0001t0001g0053a0001c0001t0001g0078others(2): Show | 5 | HG02572.hp1 NA18961.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+10374dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3052028 | |||||
| chrX:3052133
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-29+10470G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3052133 | ||||||
| chrX:3052181
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-29+10518G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3052181 | ||||||
| chrX:3052302
|
T | C | 5 | a0001c0001t0001g0029a0001c0012t0001g0086a0004c0011t0001g0024others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+10639T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3052302 | ||||||
| chrX:3052690
|
C | CA | 9 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0186others(6): Show | 9 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+11044dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3052690 | |||||
| chrX:3052690
|
C | CAA | 11 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(8): Show | 11 | HG01168.hp1 HG01169.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-29+11043_-29+1104 others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3052690 | |||||
| chrX:3052690
|
CA | C | 146 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(143): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-29+11044delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3052690 | |||||
| chrX:3052690
|
CAA | C | 5 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0077others(2): Show | 5 | HG01069.hp1 HG01934.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+11043_-29+1104 others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3052690 | |||||
| chrX:3053075
|
C | T | 2 | a0001c0001t0001g0029a0001c0012t0001g0086 | 2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-29+11412C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3053075 | ||||||
| chrX:3053328
|
C | CT | 8 | a0001c0001t0001g0029a0001c0001t0001g0078a0001c0001t0001g0158others(5): Show | 8 | HG00609.hp1 HG01192.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+11685dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3053328 | |||||
| chrX:3053328
|
C | CTT | 1 | a0001c0012t0001g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-29+11684_-29+1168 others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3053328 | |||||
| chrX:3053328
|
CT | C | 14 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(11): Show | 14 | HG00280.hp1 HG01167.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.-29+11685delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3053328 | |||||
| chrX:3053328
|
CTTTT | C | 9 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0186others(6): Show | 9 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+11682_-29+1168 others(8): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3053328 | |||||
| chrX:3053410
|
A | C | 171 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(168): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.-29+11747A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3053410 | ||||||
| chrX:3053639
|
C | T | 170 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(167): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.-29+11976C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3053639 | ||||||
| chrX:3053667
|
T | C | 9 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0186others(6): Show | 9 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+12004T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3053667 | ||||||
| chrX:3053758
|
A | AT | 12 | a0000c0014t0002g0022a0001c0001t0001g0017a0001c0001t0001g0060others(9): Show | 12 | HG00099.hp1 HG00741.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.-29+12115dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3053758 | |||||
| chrX:3053758
|
AT | A | 16 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(13): Show | 16 | HG01168.hp1 HG01169.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.-29+12115delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3053758 | |||||
| chrX:3053758
|
ATT | A | 1 | a0001c0001t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-29+12114_-29+1211 others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3053758 | |||||
| chrX:3053758
|
ATTT | A | 3 | a0002c0004t0001g0087a0002c0004t0001g0181a0002c0004t0001g0182 | 3 | HG01070.hp1 HG01071.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-29+12113_-29+1211 others(7): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3053758 | |||||
| chrX:3053760
|
T | A | 1 | a0001c0012t0001g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-29+12097T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3053760 | ||||||
| chrX:3053761
|
T | A | 1 | a0001c0001t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-29+12098T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3053761 | ||||||
| chrX:3054063
|
AC | A | 4 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+12402delC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3054063 | |||||
| chrX:3054546
|
G | A | 2 | a0001c0001t0001g0029a0001c0012t0001g0086 | 2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-29+12883G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3054546 | ||||||
| chrX:3054574
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-29+12911G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3054574 | ||||||
| chrX:3054738
|
C | CT | 2 | a0001c0005t0001g0040a0008c0019t0001g0076 | 2 | HG03098.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.-29+13089dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3054738 | |||||
| chrX:3054738
|
CT | C | 4 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0004g0188others(1): Show | 4 | HG03017.hp1 HG03490.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+13089delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3054738 | |||||
| chrX:3054762
|
T | G | 1 | a0001c0001t0001g0095 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-29+13099T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3054762 | ||||||
| chrX:3054796
|
C | A | 6 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0186others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+13133C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3054796 | ||||||
| chrX:3054803
|
G | A | 2 | a0001c0001t0001g0029a0001c0012t0001g0086 | 2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-29+13140G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3054803 | ||||||
| chrX:3054942
|
T | TA | 22 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(19): Show | 22 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-28-13131_-28-1313 others(5): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3054942 | ||||||
| chrX:3055234
|
CG | C | 1 | a0001c0001t0001g0089 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-28-12837delG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3055234 | |||||
| chrX:3055338
|
A | G | 20 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(17): Show | 20 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-28-12735A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3055338 | ||||||
| chrX:3055342
|
C | CA | 19 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0044others(16): Show | 19 | HG00597.hp2 HG00621.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.-28-12708dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3055342 | |||||
| chrX:3055342
|
C | CAA | 7 | a0001c0001t0001g0166a0001c0002t0001g0184a0001c0002t0001g0185others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28-12709_-28-1270 others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3055342 | |||||
| chrX:3055342
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0038 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-28-12719_-28-1270 others(16): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3055342 | |||||
| chrX:3055342
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0001g0035a0001c0001t0001g0036a0002c0004t0001g0182 | 3 | HG01070.hp1 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-28-12720_-28-1270 others(17): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3055342 | |||||
| chrX:3055342
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0033a0001c0001t0001g0034a0002c0004t0001g0087others(1): Show | 4 | HG01071.hp2 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-12721_-28-1270 others(18): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3055342 | |||||
| chrX:3055342
|
C | CAAAAAAA others(13): Show |
2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-28-12727_-28-1270 others(24): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3055342 | |||||
| chrX:3055342
|
CA | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0055others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.-28-12708delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3055342 | |||||
| chrX:3055566
|
T | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(8): Show | 12 | HG00738.hp1 HG01256.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-28-12507T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3055566 | ||||||
| chrX:3055589
|
C | G | 14 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(11): Show | 14 | HG01070.hp1 HG01071.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.-28-12484C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3055589 | ||||||
| chrX:3055799
|
T | A | 1 | a0001c0005t0001g0040 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-28-12274T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3055799 | ||||||
| chrX:3055877
|
C | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG00323.hp2 HG01106.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-28-12196C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3055877 | ||||||
| chrX:3055961
|
A | T | 6 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0186others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28-12112A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3055961 | ||||||
| chrX:3055969
|
C | T | 14 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(11): Show | 14 | HG01070.hp1 HG01071.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.-28-12104C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3055969 | ||||||
| chrX:3055994
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-28-12079C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3055994 | ||||||
| chrX:3055995
|
G | A | 3 | a0002c0004t0001g0087a0002c0004t0001g0181a0002c0004t0001g0182 | 3 | HG01070.hp1 HG01071.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-28-12078G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3055995 | ||||||
| chrX:3056021
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-28-12052G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3056021 | ||||||
| chrX:3056040
|
T | C | 6 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0186others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28-12033T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3056040 | ||||||
| chrX:3056181
|
A | G | 12 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-28-11892A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3056181 | ||||||
| chrX:3056253
|
G | A | 6 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0186others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28-11820G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3056253 | ||||||
| chrX:3056275
|
A | AT | 6 | a0001c0001t0001g0029a0001c0001t0001g0053a0001c0001t0001g0152others(3): Show | 6 | HG00099.hp1 HG01258.hp1 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-11780dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3056275 | |||||
| chrX:3056275
|
AT | A | 6 | a0001c0001t0001g0033a0001c0001t0001g0049a0001c0001t0001g0089others(3): Show | 6 | HG01167.hp1 HG01168.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-11780delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3056275 | |||||
| chrX:3056275
|
ATT | A | 1 | a0002c0003t0001g0012 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-28-11781_-28-1178 others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3056275 | |||||
| chrX:3056275
|
ATTTTTTT others(2): Show |
A | 1 | a0001c0001t0001g0107 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-28-11788_-28-1178 others(13): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3056275 | |||||
| chrX:3056441
|
A | G | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-28-11632A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3056441 | ||||||
| chrX:3056574
|
C | T | 6 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0186others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28-11499C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3056574 | ||||||
| chrX:3056746
|
A | G | 6 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0186others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28-11327A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3056746 | ||||||
| chrX:3056816
|
T | C | 4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(1): Show | 4 | HG02451.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-11257T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3056816 | ||||||
| chrX:3056875
|
A | T | 18 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(15): Show | 18 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-28-11198A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3056875 | ||||||
| chrX:3057053
|
C | T | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-11020C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057053 | ||||||
| chrX:3057104
|
A | AT | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-10963dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3057104 | |||||
| chrX:3057164
|
T | TC | 1 | a0001c0001t0001g0053 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-28-10908dupC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3057164 | |||||
| chrX:3057217
|
AAGTT | A | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-10855_-28-1085 others(8): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057217 | ||||||
| chrX:3057219
|
GT | G | 1 | a0001c0001t0001g0053 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-28-10851delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3057219 | |||||
| chrX:3057260
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-28-10813C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057260 | ||||||
| chrX:3057298
|
G | GT | 1 | a0001c0001t0001g0053 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-28-10768dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3057298 | |||||
| chrX:3057331
|
A | AC | 1 | a0001c0001t0001g0053 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-28-10741dupC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3057331 | |||||
| chrX:3057364
|
T | C | 20 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(17): Show | 20 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-28-10709T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057364 | ||||||
| chrX:3057384
|
A | G | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-10689A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057384 | ||||||
| chrX:3057433
|
TC | T | 1 | a0001c0001t0001g0053 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-28-10637delC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3057433 | |||||
| chrX:3057459
|
A | G | 18 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(15): Show | 18 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-28-10614A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057459 | ||||||
| chrX:3057489
|
G | A | 2 | a0001c0001t0001g0029a0001c0012t0001g0086 | 2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-28-10584G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057489 | ||||||
| chrX:3057516
|
G | A | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-10557G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057516 | ||||||
| chrX:3057517
|
T | TC | 1 | a0001c0001t0001g0053 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-28-10555dupC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3057517 | |||||
| chrX:3057532
|
A | AG | 1 | a0001c0001t0001g0053 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-28-10539dupG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3057532 | |||||
| chrX:3057574
|
A | AG | 1 | a0001c0001t0001g0053 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-28-10498dupG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3057574 | |||||
| chrX:3057604
|
G | GA | 1 | a0001c0001t0001g0053 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-28-10469_-28-1046 others(5): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057604 | ||||||
| chrX:3057650
|
AT | A | 1 | a0001c0001t0001g0053 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-28-10420delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3057650 | |||||
| chrX:3057729
|
A | AT | 1 | a0001c0001t0001g0053 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-28-10343dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3057729 | |||||
| chrX:3057916
|
G | A | 17 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(14): Show | 17 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28-10157G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057916 | ||||||
| chrX:3057946
|
G | A | 1 | a0001c0002t0001g0186 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-28-10127G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057946 | ||||||
| chrX:3058065
|
C | T | 19 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-28-10008C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058065 | ||||||
| chrX:3058289
|
T | TG | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-9784_-28-9783i others(3): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058289 | ||||||
| chrX:3058298
|
G | A | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-9775G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058298 | ||||||
| chrX:3058339
|
C | G | 1 | a0001c0001t0001g0049 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-28-9734C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058339 | ||||||
| chrX:3058426
|
C | T | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-9647C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058426 | ||||||
| chrX:3058453
|
G | C | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-9620G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058453 | ||||||
| chrX:3058645
|
G | A | 17 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(14): Show | 17 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28-9428G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058645 | ||||||
| chrX:3058673
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(1): Show | 4 | NA18957.hp1 NA18988.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-9400G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058673 | ||||||
| chrX:3058674
|
G | A | 17 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(14): Show | 17 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28-9399G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058674 | ||||||
| chrX:3058759
|
G | T | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-9314G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058759 | ||||||
| chrX:3058832
|
A | G | 19 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-28-9241A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058832 | ||||||
| chrX:3058929
|
T | C | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-9144T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058929 | ||||||
| chrX:3059190
|
C | T | 5 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0170others(2): Show | 5 | HG01515.hp1 HG01517.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28-8883C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059190 | ||||||
| chrX:3059353
|
C | T | 2 | a0001c0001t0001g0029a0001c0012t0001g0086 | 2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-28-8720C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059353 | ||||||
| chrX:3059388
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-28-8685C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059388 | ||||||
| chrX:3059527
|
T | A | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-8546T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059527 | ||||||
| chrX:3059553
|
T | A | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-28-8520T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059553 | ||||||
| chrX:3059643
|
C | A | 3 | a0002c0004t0001g0087a0002c0004t0001g0181a0002c0004t0001g0182 | 3 | HG01070.hp1 HG01071.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-28-8430C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059643 | ||||||
| chrX:3059647
|
C | T | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-8426C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059647 | ||||||
| chrX:3059649
|
C | G | 4 | a0001c0001t0001g0051a0001c0001t0001g0101a0001c0001t0001g0149others(1): Show | 4 | HG00673.hp1 HG02027.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-8424C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059649 | ||||||
| chrX:3059729
|
G | T | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-8344G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059729 | ||||||
| chrX:3059971
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-28-8102G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059971 | ||||||
| chrX:3059995
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-28-8078C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059995 | ||||||
| chrX:3060027
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-28-8046C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060027 | ||||||
| chrX:3060220
|
T | C | 21 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(18): Show | 21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-28-7853T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060220 | ||||||
| chrX:3060253
|
A | G | 1 | a0001c0015t0007g0018 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-28-7820A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060253 | ||||||
| chrX:3060373
|
G | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0175 | 3 | NA18951.hp1 NA18994.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-28-7700G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060373 | ||||||
| chrX:3060396
|
T | G | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-7677T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060396 | ||||||
| chrX:3060430
|
C | T | 17 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(14): Show | 17 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28-7643C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060430 | ||||||
| chrX:3060442
|
G | C | 19 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-28-7631G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060442 | ||||||
| chrX:3060529
|
A | G | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-7544A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060529 | ||||||
| chrX:3060641
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-28-7432C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060641 | ||||||
| chrX:3060895
|
A | G | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-7178A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060895 | ||||||
| chrX:3060957
|
T | C | 1 | a0001c0001t0001g0113 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-28-7116T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060957 | ||||||
| chrX:3061028
|
A | C | 1 | a0001c0001t0001g0053 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-28-7045A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3061028 | ||||||
| chrX:3061198
|
T | A | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-6875T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3061198 | ||||||
| chrX:3061601
|
G | A | 2 | a0001c0001t0001g0029a0001c0012t0001g0086 | 2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-28-6472G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3061601 | ||||||
| chrX:3061602
|
G | A | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-6471G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3061602 | ||||||
| chrX:3061628
|
A | C | 149 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(146): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.-28-6445A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3061628 | ||||||
| chrX:3061685
|
G | A | 1 | a0001c0002t0001g0013 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-28-6388G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3061685 | ||||||
| chrX:3061872
|
T | A | 1 | a0001c0015t0007g0018 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-28-6201T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3061872 | ||||||
| chrX:3061893
|
C | T | 4 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037others(1): Show | 4 | HG02280.hp1 HG02809.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-6180C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3061893 | ||||||
| chrX:3061937
|
C | T | 1 | a0001c0007t0003g0183 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-28-6136C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3061937 | ||||||
| chrX:3062168
|
A | G | 17 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(14): Show | 17 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28-5905A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062168 | ||||||
| chrX:3062300
|
A | G | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-5773A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062300 | ||||||
| chrX:3062355
|
T | G | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-5718T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062355 | ||||||
| chrX:3062516
|
T | C | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-5557T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062516 | ||||||
| chrX:3062551
|
C | T | 4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(1): Show | 4 | HG02451.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-5522C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062551 | ||||||
| chrX:3062620
|
A | T | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-5453A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062620 | ||||||
| chrX:3062659
|
G | A | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-5414G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062659 | ||||||
| chrX:3062686
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-28-5387A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062686 | ||||||
| chrX:3062716
|
A | C | 1 | a0001c0001t0001g0147 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-28-5357A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062716 | ||||||
| chrX:3062720
|
T | C | 20 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(17): Show | 20 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-28-5353T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062720 | ||||||
| chrX:3062722
|
T | C | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-5351T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062722 | ||||||
| chrX:3062746
|
TA | T | 1 | a0001c0001t0001g0042 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-28-5324delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3062746 | |||||
| chrX:3062971
|
T | C | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-5102T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062971 | ||||||
| chrX:3063122
|
C | T | 1 | a0001c0012t0001g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-28-4951C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3063122 | ||||||
| chrX:3063434
|
A | G | 1 | a0002c0003t0001g0146 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-28-4639A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3063434 | ||||||
| chrX:3063435
|
G | C | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-4638G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3063435 | ||||||
| chrX:3063463
|
G | A | 17 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(14): Show | 17 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28-4610G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3063463 | ||||||
| chrX:3063486
|
T | A | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-4587T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3063486 | ||||||
| chrX:3063794
|
C | G | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-4279C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3063794 | ||||||
| chrX:3063944
|
G | GA | 2 | a0001c0001t0001g0078a0001c0001t0001g0114 | 2 | NA18961.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-28-4124dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3063944 | |||||
| chrX:3063973
|
C | CA | 1 | a0001c0001t0001g0114 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-28-4094dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3063973 | |||||
| chrX:3064138
|
G | GA | 1 | a0001c0001t0001g0114 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-28-3932dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3064138 | |||||
| chrX:3064360
|
C | T | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-3713C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3064360 | ||||||
| chrX:3064427
|
G | T | 1 | a0001c0002t0001g0021 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-28-3646G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3064427 | ||||||
| chrX:3064467
|
TA | T | 1 | a0001c0001t0001g0114 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-28-3603delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3064467 | |||||
| chrX:3064470
|
A | C | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-3603A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3064470 | ||||||
| chrX:3064583
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-28-3490A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3064583 | ||||||
| chrX:3064617
|
A | AC | 1 | a0001c0001t0001g0114 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-28-3455dupC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3064617 | |||||
| chrX:3064748
|
C | A | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-3325C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3064748 | ||||||
| chrX:3064854
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | NA18952.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-28-3219G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3064854 | ||||||
| chrX:3064957
|
A | G | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-3116A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3064957 | ||||||
| chrX:3065211
|
C | A | 1 | a0001c0002t0001g0065 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-28-2862C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065211 | ||||||
| chrX:3065284
|
T | TG | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-28-2785dupG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3065284 | |||||
| chrX:3065297
|
T | G | 21 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(18): Show | 21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-28-2776T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065297 | ||||||
| chrX:3065313
|
T | C | 2 | a0001c0001t0001g0108a0003c0008t0001g0115 | 2 | HG02258.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.-28-2760T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065313 | ||||||
| chrX:3065321
|
G | A | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-2752G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065321 | ||||||
| chrX:3065353
|
C | T | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-2720C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065353 | ||||||
| chrX:3065435
|
AAAAT | A | 3 | a0001c0007t0003g0028a0001c0007t0003g0183a0001c0012t0001g0086 | 3 | HG02257.hp2 HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-28-2610_-28-2607d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3065435 | |||||
| chrX:3065459
|
T | G | 1 | a0004c0011t0001g0031 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-28-2614T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065459 | ||||||
| chrX:3065479
|
G | GA | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-2586dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3065479 | |||||
| chrX:3065636
|
C | CA | 11 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(8): Show | 11 | HG00323.hp2 HG01168.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.-28-2422dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3065636 | |||||
| chrX:3065636
|
C | CAA | 11 | a0001c0001t0001g0032a0001c0002t0001g0184a0001c0002t0001g0185others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-28-2423_-28-2422d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3065636 | |||||
| chrX:3065636
|
C | CAAA | 1 | a0001c0001t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-28-2424_-28-2422d others(5): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3065636 | |||||
| chrX:3065636
|
C | CCA | 3 | a0001c0007t0003g0028a0001c0007t0003g0183a0001c0012t0001g0086 | 3 | HG02257.hp2 HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-28-2437_-28-2436i others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065636 | ||||||
| chrX:3065636
|
CA | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0094a0001c0001t0001g0145 | 3 | HG03017.hp1 NA18961.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-28-2422delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3065636 | |||||
| chrX:3065797
|
A | G | 21 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(18): Show | 21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-28-2276A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065797 | ||||||
| chrX:3065825
|
G | A | 20 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(17): Show | 20 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-28-2248G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065825 | ||||||
| chrX:3065857
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-28-2216G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065857 | ||||||
| chrX:3065913
|
A | G | 20 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(17): Show | 20 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-28-2160A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065913 | ||||||
| chrX:3066232
|
A | T | 1 | a0001c0012t0001g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-28-1841A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3066232 | ||||||
| chrX:3066308
|
C | T | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-1765C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3066308 | ||||||
| chrX:3066426
|
T | A | 1 | a0001c0012t0001g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-28-1647T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3066426 | ||||||
| chrX:3066538
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-28-1535G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3066538 | ||||||
| chrX:3066626
|
T | C | 4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(1): Show | 4 | HG02451.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-1447T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3066626 | ||||||
| chrX:3066791
|
C | CA | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-28-1281dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3066791 | |||||
| chrX:3066845
|
G | C | 1 | a0001c0012t0001g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-28-1228G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3066845 | ||||||
| chrX:3066901
|
A | AT | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-28-1168dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3066901 | |||||
| chrX:3066912
|
C | CT | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-28-1145dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3066912 | |||||
| chrX:3066912
|
CT | C | 145 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(142): Show | 149 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-28-1145delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3066912 | |||||
| chrX:3066912
|
CTT | C | 7 | a0001c0001t0001g0053a0001c0001t0001g0059a0001c0001t0001g0074others(4): Show | 7 | HG00323.hp2 HG03017.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28-1146_-28-1145d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3066912 | |||||
| chrX:3066945
|
G | A | 3 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183 | 3 | HG02257.hp2 HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-28-1128G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3066945 | ||||||
| chrX:3066981
|
T | C | 3 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183 | 3 | HG02257.hp2 HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-28-1092T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3066981 | ||||||
| chrX:3067067
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-28-1006C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067067 | ||||||
| chrX:3067104
|
C | T | 18 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(15): Show | 18 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-28-969C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067104 | ||||||
| chrX:3067125
|
C | CA | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-28-946dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3067125 | |||||
| chrX:3067131
|
C | CGT | 2 | a0001c0005t0001g0007a0001c0005t0001g0009 | 2 | HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-28-924_-28-923dup others(2): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3067131 | |||||
| chrX:3067131
|
CGTGT | C | 21 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(18): Show | 21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-28-926_-28-923del others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3067131 | |||||
| chrX:3067162
|
G | GT | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-28-910dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3067162 | |||||
| chrX:3067193
|
T | A | 18 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(15): Show | 18 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-28-880T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067193 | ||||||
| chrX:3067200
|
T | TA | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-28-872dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3067200 | |||||
| chrX:3067201
|
A | T | 1 | a0001c0001t0001g0162 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-28-872A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067201 | ||||||
| chrX:3067202
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-28-871T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067202 | ||||||
| chrX:3067203
|
A | C | 22 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(19): Show | 22 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-28-870A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067203 | ||||||
| chrX:3067260
|
G | GT | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-28-811dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3067260 | |||||
| chrX:3067280
|
T | G | 1 | a0001c0001t0001g0117 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-28-793T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067280 | ||||||
| chrX:3067372
|
CA | C | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-28-699delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3067372 | |||||
| chrX:3067379
|
A | AT | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-28-693dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3067379 | |||||
| chrX:3067387
|
A | G | 1 | a0002c0003t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-28-686A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067387 | ||||||
| chrX:3067416
|
C | T | 148 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(145): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.-28-657C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067416 | ||||||
| chrX:3067449
|
T | TG | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-28-623dupG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3067449 | |||||
| chrX:3067631
|
G | A | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-28-442G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067631 | ||||||
| chrX:3067713
|
G | GA | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-28-360_-28-359ins others(1): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067713 | ||||||
| chrX:3067731
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-28-342C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067731 | ||||||
| chrX:3067740
|
T | TC | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-28-329dupC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3067740 | |||||
| chrX:3067840
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-28-233C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067840 | ||||||
| chrX:3067852
|
G | A | 1 | a0001c0012t0001g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-28-221G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067852 | ||||||
| chrX:3067856
|
C | CA | 29 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0033others(26): Show | 30 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.-28-203dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3067856 | |||||
| chrX:3067874
|
CA | C | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-28-195delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3067874 | |||||
| chrX:3068020
|
C | CT | 7 | a0001c0001t0001g0029a0001c0001t0001g0078a0001c0001t0001g0142others(4): Show | 7 | HG02257.hp2 HG02486.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28-36dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3068020 | |||||
| chrX:3068020
|
CT | C | 8 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(5): Show | 8 | HG02056.hp1 HG02572.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28-36delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3068020 | |||||
| chrX:3068020
|
CTT | C | 17 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(14): Show | 17 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28-37_-28-36delTT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3068020 | |||||
| chrX:3068070
|
A | G | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.-28-3A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3068070 | ||||||
| chrX:3068185
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.11+74C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3068185 | ||||||
| chrX:3068221
|
T | A | 19 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.11+110T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3068221 | ||||||
| chrX:3068224
|
C | CT | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.11+119dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3068224 | |||||
| chrX:3068275
|
T | TA | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.11+165dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3068275 | |||||
| chrX:3068314
|
A | AC | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.11+204dupC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3068314 | |||||
| chrX:3068337
|
T | TA | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.11+231dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3068337 | |||||
| chrX:3068412
|
A | AT | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.11+306dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3068412 | |||||
| chrX:3068572
|
G | A | 4 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(1): Show | 4 | HG02257.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.11+461G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3068572 | ||||||
| chrX:3068610
|
A | AG | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.11+500dupG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3068610 | |||||
| chrX:3068731
|
T | TA | 1 | a0001c0001t0001g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.11+621dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3068731 | |||||
| chrX:3068762
|
G | A | 7 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+651G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3068762 | ||||||
| chrX:3068765
|
G | GATA | 7 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+655_11+656insTA others(1): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3068765 | |||||
| chrX:3068806
|
A | G | 7 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+695A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3068806 | ||||||
| chrX:3068888
|
A | G | 7 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+777A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3068888 | ||||||
| chrX:3068907
|
C | A | 7 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+796C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3068907 | ||||||
| chrX:3069033
|
C | G | 7 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+922C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3069033 | ||||||
| chrX:3069169
|
A | G | 1 | a0001c0012t0001g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.11+1058A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3069169 | ||||||
| chrX:3069321
|
C | T | 4 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(1): Show | 4 | HG02257.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.11+1210C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3069321 | ||||||
| chrX:3069332
|
C | CT | 7 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+1226dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3069332 | |||||
| chrX:3069338
|
C | T | 7 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+1227C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3069338 | ||||||
| chrX:3069359
|
T | C | 1 | a0001c0016t0001g0156 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.11+1248T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3069359 | ||||||
| chrX:3069385
|
G | A | 4 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(1): Show | 4 | HG02257.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.11+1274G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3069385 | ||||||
| chrX:3069498
|
A | AT | 7 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+1394dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3069498 | |||||
| chrX:3069568
|
C | T | 7 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+1457C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3069568 | ||||||
| chrX:3069697
|
C | CT | 7 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+1591dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3069697 | |||||
| chrX:3069720
|
T | TA | 7 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+1610dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3069720 | |||||
| chrX:3069721
|
A | AT | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.11+1617dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3069721 | |||||
| chrX:3069722
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.11+1611T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3069722 | ||||||
| chrX:3069875
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.11+1764C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3069875 | ||||||
| chrX:3070240
|
C | T | 1 | a0004c0023t0001g0169 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.12-1786C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3070240 | ||||||
| chrX:3070315
|
A | G | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.12-1711A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3070315 | ||||||
| chrX:3070368
|
T | C | 170 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(167): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.12-1658T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3070368 | ||||||
| chrX:3070590
|
A | T | 179 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(176): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.12-1436A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3070590 | ||||||
| chrX:3070686
|
T | C | 1 | a0002c0003t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.12-1340T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3070686 | ||||||
| chrX:3070768
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.12-1258T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3070768 | ||||||
| chrX:3070775
|
G | A | 3 | a0001c0012t0001g0086a0005c0006t0001g0005a0005c0006t0001g0006 | 3 | HG01168.hp1 HG01169.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.12-1251G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3070775 | ||||||
| chrX:3070917
|
T | TA | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.12-1108dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3070917 | |||||
| chrX:3070938
|
G | GGT | 20 | a0001c0001t0001g0032a0001c0001t0001g0038a0001c0001t0001g0043others(17): Show | 20 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.12-1055_12-1054dup others(2): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3070938 | |||||
| chrX:3070938
|
G | GGTGT | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 5 | HG02451.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.12-1057_12-1054dup others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3070938 | |||||
| chrX:3070938
|
GGT | G | 135 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(132): Show | 139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.12-1055_12-1054del others(2): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3070938 | |||||
| chrX:3070938
|
GGTGTGT | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0007t0003g0028others(2): Show | 5 | HG00738.hp1 HG02257.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.12-1059_12-1054del others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3070938 | |||||
| chrX:3070994
|
GGATA | G | 148 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(145): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.12-1023_12-1020del others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3070994 | |||||
| chrX:3071099
|
C | T | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.12-927C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3071099 | ||||||
| chrX:3071193
|
T | C | 1 | a0001c0002t0001g0013 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.12-833T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3071193 | ||||||
| chrX:3071249
|
A | G | 20 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(17): Show | 20 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.12-777A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3071249 | ||||||
| chrX:3071291
|
T | TTTG | 4 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.12-708_12-706dupGT others(1): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3071291 | |||||
| chrX:3071291
|
T | TTTGTTG | 1 | a0001c0012t0001g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.12-711_12-706dupGT others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3071291 | |||||
| chrX:3071291
|
TTTGTTG | T | 1 | a0001c0001t0001g0067 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.12-711_12-706delGT others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3071291 | |||||
| chrX:3071425
|
C | T | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.12-601C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3071425 | ||||||
| chrX:3071599
|
C | T | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.12-427C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3071599 | ||||||
| chrX:3071643
|
G | T | 4 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(1): Show | 4 | HG02257.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.12-383G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3071643 | ||||||
| chrX:3071677
|
A | G | 7 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.12-349A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3071677 | ||||||
| chrX:3072220
|
G | C | 4 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(1): Show | 4 | HG02257.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+45G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3072220 | ||||||
| chrX:3072269
|
T | C | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.161+94T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3072269 | ||||||
| chrX:3072279
|
C | CT | 21 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(18): Show | 21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.161+112dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3072279 | |||||
| chrX:3072578
|
A | G | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+403A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3072578 | ||||||
| chrX:3072634
|
G | C | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+459G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3072634 | ||||||
| chrX:3072742
|
T | C | 1 | a0001c0012t0001g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.161+567T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3072742 | ||||||
| chrX:3072849
|
A | C | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.161+674A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3072849 | ||||||
| chrX:3072884
|
C | T | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+709C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3072884 | ||||||
| chrX:3072952
|
A | G | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+777A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3072952 | ||||||
| chrX:3072963
|
C | T | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+788C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3072963 | ||||||
| chrX:3073033
|
T | A | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+858T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073033 | ||||||
| chrX:3073072
|
C | T | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.161+897C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073072 | ||||||
| chrX:3073096
|
G | C | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+921G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073096 | ||||||
| chrX:3073237
|
TTA | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(63): Show | 69 | HG00099.hp2 HG00323.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.161+1071_161+1072d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3073237 | |||||
| chrX:3073273
|
A | G | 4 | a0001c0002t0001g0011a0001c0002t0001g0025a0001c0002t0001g0026others(1): Show | 4 | HG00642.hp1 HG00735.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+1098A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073273 | ||||||
| chrX:3073356
|
T | C | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+1181T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073356 | ||||||
| chrX:3073531
|
T | G | 21 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(18): Show | 21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.161+1356T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073531 | ||||||
| chrX:3073533
|
A | ATATAGTA others(128): Show |
2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+1358_161+1359i others(137): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073533 | ||||||
| chrX:3073533
|
A | ATATAGTA others(86): Show |
2 | a0002c0004t0001g0181a0002c0004t0001g0182 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.161+1358_161+1359i others(95): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073533 | ||||||
| chrX:3073533
|
A | ATATAGTA others(144): Show |
1 | a0001c0001t0001g0029 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.161+1358_161+1359i others(153): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073533 | ||||||
| chrX:3073533
|
A | ATATAGTA others(93): Show |
12 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(9): Show | 12 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.161+1358_161+1359i others(102): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073533 | ||||||
| chrX:3073533
|
A | ATATAGTA others(100): Show |
1 | a0001c0001t0001g0036 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.161+1358_161+1359i others(109): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073533 | ||||||
| chrX:3073533
|
A | ATATAGTA others(158): Show |
1 | a0002c0003t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.161+1358_161+1359i others(167): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073533 | ||||||
| chrX:3073533
|
A | ATATAGTA others(172): Show |
2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.161+1358_161+1359i others(181): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073533 | ||||||
| chrX:3073536
|
A | T | 21 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(18): Show | 21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.161+1361A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073536 | ||||||
| chrX:3073545
|
T | C | 21 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(18): Show | 21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.161+1370T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073545 | ||||||
| chrX:3073548
|
ATT | A | 1 | a0004c0011t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.161+1374_161+1375d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073548 | ||||||
| chrX:3073585
|
A | ATATTTAT others(39): Show |
2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+1415_161+1416i others(48): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3073585 | |||||
| chrX:3073669
|
A | AAT | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+1500_161+1501d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3073669 | |||||
| chrX:3073680
|
A | AATAAATA others(27): Show |
1 | a0001c0001t0001g0098 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.161+1520_161+1553d others(36): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3073680 | |||||
| chrX:3073680
|
A | AATAAATA others(129): Show |
2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+1553_161+1554i others(138): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3073680 | |||||
| chrX:3073713
|
A | T | 1 | a0001c0001t0001g0074 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.161+1538A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073713 | ||||||
| chrX:3073751
|
A | ATATT | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+1579_161+1580i others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3073751 | |||||
| chrX:3073826
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.161+1651T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073826 | ||||||
| chrX:3073998
|
G | A | 19 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.161+1823G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073998 | ||||||
| chrX:3074101
|
C | T | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.161+1926C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3074101 | ||||||
| chrX:3074148
|
G | C | 21 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(18): Show | 21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.161+1973G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3074148 | ||||||
| chrX:3074436
|
C | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 6 | HG00738.hp1 HG01256.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-2112C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3074436 | ||||||
| chrX:3074586
|
T | C | 21 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(18): Show | 21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.162-1962T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3074586 | ||||||
| chrX:3074809
|
C | T | 22 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(19): Show | 22 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.162-1739C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3074809 | ||||||
| chrX:3074856
|
C | T | 22 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(19): Show | 22 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.162-1692C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3074856 | ||||||
| chrX:3074869
|
G | C | 22 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(19): Show | 22 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.162-1679G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3074869 | ||||||
| chrX:3075070
|
C | T | 22 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(19): Show | 22 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.162-1478C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3075070 | ||||||
| chrX:3075101
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.162-1447G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3075101 | ||||||
| chrX:3075450
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.162-1098T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3075450 | ||||||
| chrX:3075451
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.162-1097G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3075451 | ||||||
| chrX:3075488
|
G | GTC | 179 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(176): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.162-1056_162-1055d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3075488 | |||||
| chrX:3075741
|
G | T | 147 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(144): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.162-807G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3075741 | ||||||
| chrX:3075746
|
T | C | 1 | a0001c0012t0001g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.162-802T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3075746 | ||||||
| chrX:3075897
|
CTCTG | C | 151 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(148): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.162-649_162-646del others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3075897 | |||||
| chrX:3075943
|
G | A | 15 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.162-605G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3075943 | ||||||
| chrX:3075983
|
G | GTC | 151 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(148): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.162-561_162-560dup others(2): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3075983 | |||||
| chrX:3076105
|
TTCTC | T | 2 | a0001c0001t0001g0107a0001c0001t0004g0188 | 2 | HG03669.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.162-435_162-432del others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3076105 | |||||
| chrX:3076113
|
CTCTG | C | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | NA18955.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.162-431_162-428del others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3076113 | |||||
| chrX:3076336
|
GTC | G | 152 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(149): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.162-200_162-199del others(2): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3076336 | |||||
| chrX:3076386
|
C | G | 1 | a0001c0001t0001g0016 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.162-162C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3076386 | ||||||
| chrX:3076393
|
T | C | 153 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(150): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.162-155T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3076393 | ||||||
| chrX:3076394
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.162-154G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3076394 | ||||||
| chrX:3076498
|
G | GC | 1 | a0006c0022t0001g0174 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.162-44dupC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3076498 | |||||
| chrX:3076509
|
T | C | 4 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(1): Show | 4 | HG02257.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.162-39T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3076509 | ||||||
| chrX:3076684
|
G | A | 8 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(5): Show | 8 | HG02071.hp1 NA18612.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+15G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3076684 | ||||||
| chrX:3076702
|
C | T | 1 | a0002c0003t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.283+33C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3076702 | ||||||
| chrX:3076770
|
C | T | 1 | a0001c0002t0001g0019 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.283+101C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3076770 | ||||||
| chrX:3076803
|
G | A | 3 | a0002c0004t0001g0087a0002c0004t0001g0181a0002c0004t0001g0182 | 3 | HG01070.hp1 HG01071.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.283+134G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3076803 | ||||||
| chrX:3076855
|
G | C | 1 | a0001c0001t0001g0053 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.283+186G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3076855 | ||||||
| chrX:3076892
|
T | A | 3 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183 | 3 | HG02257.hp2 HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.283+223T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3076892 | ||||||
| chrX:3077036
|
G | A | 147 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(144): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.283+367G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3077036 | ||||||
| chrX:3077375
|
A | G | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283+706A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3077375 | ||||||
| chrX:3077456
|
C | A | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283+787C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3077456 | ||||||
| chrX:3077554
|
G | A | 148 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(145): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.283+885G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3077554 | ||||||
| chrX:3077788
|
A | T | 1 | a0001c0005t0001g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.283+1119A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3077788 | ||||||
| chrX:3077789
|
T | TATTATTA others(3): Show |
1 | a0001c0005t0001g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.283+1120_283+1121i others(12): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3077789 | ||||||
| chrX:3077789
|
T | TTTA | 1 | a0006c0022t0001g0174 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.283+1147_283+1149d others(5): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3077789 | |||||
| chrX:3077789
|
T | TTTATTA | 5 | a0001c0001t0001g0038a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG01192.hp1 HG02486.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+1144_283+1149d others(8): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3077789 | |||||
| chrX:3077789
|
T | TTTATTAT others(2): Show |
9 | a0001c0001t0001g0075a0001c0001t0001g0140a0001c0001t0001g0159others(6): Show | 9 | HG00099.hp2 HG01074.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+1141_283+1149d others(11): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3077789 | |||||
| chrX:3077789
|
T | TTTATTAT others(5): Show |
40 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0016others(37): Show | 41 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.283+1138_283+1149d others(14): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3077789 | |||||
| chrX:3077789
|
T | TTTATTAT others(8): Show |
51 | a0001c0001t0001g0003a0001c0001t0001g0049a0001c0001t0001g0050others(48): Show | 52 | HG00323.hp2 HG00621.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.283+1135_283+1149d others(17): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3077789 | |||||
| chrX:3077789
|
T | TTTATTAT others(11): Show |
30 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(27): Show | 32 | HG00597.hp2 HG00735.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.283+1132_283+1149d others(20): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3077789 | |||||
| chrX:3077789
|
T | TTTATTAT others(14): Show |
12 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(9): Show | 12 | HG00738.hp1 HG01256.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+1129_283+1149d others(23): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3077789 | |||||
| chrX:3077789
|
T | TTTATTAT others(17): Show |
1 | a0001c0001t0001g0072 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.283+1126_283+1149d others(26): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3077789 | |||||
| chrX:3077789
|
T | TTTTTTAT others(5): Show |
2 | a0001c0001t0001g0088a0001c0020t0001g0092 | 2 | HG02735.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.283+1122_283+1123i others(14): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3077789 | |||||
| chrX:3077857
|
T | G | 151 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(148): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.283+1188T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3077857 | ||||||
| chrX:3078079
|
T | C | 155 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(152): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.283+1410T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3078079 | ||||||
| chrX:3078099
|
C | T | 3 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183 | 3 | HG02257.hp2 HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.283+1430C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3078099 | ||||||
| chrX:3078121
|
A | G | 148 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(145): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.283+1452A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3078121 | ||||||
| chrX:3078239
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(70): Show | 76 | HG00099.hp2 HG00323.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.283+1570G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3078239 | ||||||
| chrX:3078418
|
G | A | 148 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(145): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.283+1749G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3078418 | ||||||
| chrX:3078648
|
C | T | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283+1979C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3078648 | ||||||
| chrX:3078653
|
C | T | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283+1984C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3078653 | ||||||
| chrX:3078951
|
C | T | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.284-1940C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3078951 | ||||||
| chrX:3079028
|
C | T | 148 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(145): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.284-1863C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3079028 | ||||||
| chrX:3079342
|
A | AT | 3 | a0000c0014t0002g0022a0001c0007t0003g0028a0001c0007t0003g0183 | 3 | HG01884.hp1 HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.284-1529dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3079342 | |||||
| chrX:3079342
|
AT | A | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG00323.hp1 NA18957.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-1529delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3079342 | |||||
| chrX:3079342
|
ATT | A | 134 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(131): Show | 138 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.284-1530_284-1529d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3079342 | |||||
| chrX:3079342
|
ATTT | A | 9 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0066others(6): Show | 9 | HG00140.hp1 HG01255.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-1531_284-1529d others(5): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3079342 | |||||
| chrX:3079439
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.284-1452G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3079439 | ||||||
| chrX:3079462
|
A | G | 4 | a0001c0001t0001g0029a0001c0007t0003g0028a0001c0007t0003g0183others(1): Show | 4 | HG02257.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-1429A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3079462 | ||||||
| chrX:3079533
|
G | A | 2 | a0005c0006t0001g0005a0005c0006t0001g0006 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.284-1358G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3079533 | ||||||
| chrX:3079957
|
T | TCAA | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0010t0001g0030 | 3 | HG02280.hp1 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.284-921_284-919dup others(3): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3079957 | |||||
| chrX:3079967
|
C | CA | 1 | a0001c0001t0001g0149 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.284-922dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3079967 | |||||
| chrX:3079970
|
C | A | 1 | a0001c0001t0001g0149 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.284-921C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3079970 | ||||||
| chrX:3079970
|
C | CA | 13 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0051others(10): Show | 13 | HG00673.hp1 HG00735.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-899dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3079970 | |||||
| chrX:3079970
|
C | CAA | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.284-900_284-899dup others(2): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3079970 | |||||
| chrX:3079970
|
CA | C | 12 | a0001c0001t0001g0016a0001c0001t0001g0043a0001c0001t0001g0046others(9): Show | 12 | HG01070.hp1 HG01168.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-899delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3079970 | |||||
| chrX:3079970
|
CAA | C | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.284-900_284-899del others(2): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3079970 | |||||
| chrX:3079973
|
A | C | 2 | a0001c0001t0001g0032a0001c0010t0001g0037 | 2 | HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.284-918A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3079973 | ||||||
| chrX:3079993
|
G | A | 2 | a0001c0001t0001g0032a0001c0010t0001g0037 | 2 | HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.284-898G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3079993 | ||||||
| chrX:3080003
|
GA | G | 1 | a0001c0010t0001g0030 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.284-876delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3080003 | |||||
| chrX:3080004
|
A | AG | 2 | a0001c0001t0001g0032a0001c0010t0001g0037 | 2 | HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.284-887_284-886ins others(1): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080004 | ||||||
| chrX:3080005
|
A | G | 155 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(152): Show | 159 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.284-886A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080005 | ||||||
| chrX:3080006
|
A | G | 3 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037 | 3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.284-885A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080006 | ||||||
| chrX:3080101
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.284-790G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080101 | ||||||
| chrX:3080186
|
T | A | 1 | a0001c0001t0001g0176 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.284-705T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080186 | ||||||
| chrX:3080255
|
CATGAGGT others(30): Show |
C | 148 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(145): Show | 152 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.284-631_284-595del others(37): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3080255 | |||||
| chrX:3080265
|
G | A | 3 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037 | 3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.284-626G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080265 | ||||||
| chrX:3080286
|
C | T | 3 | a0002c0004t0001g0087a0002c0004t0001g0181a0002c0004t0001g0182 | 3 | HG01070.hp1 HG01071.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.284-605C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080286 | ||||||
| chrX:3080358
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-533C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080358 | ||||||
| chrX:3080433
|
T | C | 187 | a0000c0014t0002g0022a0000c0018t0002g0129a0001c0001t0001g0001others(184): Show | 191 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.284-458T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080433 | ||||||
| chrX:3080450
|
G | A | 1 | a0001c0015t0007g0018 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.284-441G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080450 | ||||||
| chrX:3080459
|
C | T | 157 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(154): Show | 161 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.284-432C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080459 | ||||||
| chrX:3080472
|
C | CA | 152 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(149): Show | 156 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.284-406dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3080472 | |||||
| chrX:3080472
|
C | CAA | 2 | a0001c0001t0001g0119a0001c0001t0001g0166 | 2 | NA18965.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.284-407_284-406dup others(2): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3080472 | |||||
| chrX:3080649
|
G | A | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.284-242G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080649 | ||||||
| chrX:3080771
|
G | A | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.284-120G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080771 | ||||||
| chrX:3080855
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.284-36A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080855 | ||||||
| chrX:3081100
|
G | A | 162 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(159): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.406+87G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3081100 | ||||||
| chrX:3081130
|
G | A | 1 | a0001c0002t0001g0126 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.406+117G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3081130 | ||||||
| chrX:3081460
|
T | C | 162 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(159): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.406+447T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3081460 | ||||||
| chrX:3081481
|
C | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG01099.hp1 HG01496.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.406+468C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3081481 | ||||||
| chrX:3081493
|
C | T | 3 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037 | 3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.406+480C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3081493 | ||||||
| chrX:3081807
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.406+794A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3081807 | ||||||
| chrX:3082125
|
A | G | 6 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.406+1112A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3082125 | ||||||
| chrX:3082133
|
C | T | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.406+1120C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3082133 | ||||||
| chrX:3082346
|
C | A | 1 | a0001c0001t0001g0149 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.406+1333C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3082346 | ||||||
| chrX:3082698
|
C | A | 1 | a0001c0001t0001g0091 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.407-1545C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3082698 | ||||||
| chrX:3082960
|
CTATCT | C | 6 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.407-1277_407-1273d others(7): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3082960 | |||||
| chrX:3082965
|
T | G | 3 | a0002c0004t0001g0087a0002c0004t0001g0181a0002c0004t0001g0182 | 3 | HG01070.hp1 HG01071.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.407-1278T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3082965 | ||||||
| chrX:3083023
|
TTATC | T | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.407-1211_407-1208d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083023 | |||||
| chrX:3083064
|
ATATC | A | 5 | a0001c0001t0001g0032a0001c0001t0001g0035a0001c0001t0001g0036others(2): Show | 5 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.407-1163_407-1160d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083064 | |||||
| chrX:3083092
|
C | CCTAT | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.407-1141_407-1138d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083092 | |||||
| chrX:3083092
|
CCTAT | C | 1 | a0001c0001t0001g0132 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.407-1141_407-1138d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083092 | |||||
| chrX:3083225
|
A | G | 1 | a0002c0003t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.407-1018A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3083225 | ||||||
| chrX:3083388
|
C | G | 1 | a0001c0001t0001g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.407-855C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3083388 | ||||||
| chrX:3083404
|
C | A | 3 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037 | 3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.407-839C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3083404 | ||||||
| chrX:3083440
|
G | A | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.407-803G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3083440 | ||||||
| chrX:3083481
|
C | CCTAT | 1 | a0006c0022t0001g0174 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.407-716_407-713dup others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083481 | |||||
| chrX:3083481
|
CCTAT | C | 14 | a0000c0014t0002g0022a0001c0002t0001g0011a0001c0002t0001g0013others(11): Show | 14 | HG00323.hp1 HG00735.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.407-716_407-713del others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083481 | |||||
| chrX:3083481
|
CCTATCTA others(1): Show |
C | 3 | a0001c0002t0001g0025a0001c0002t0001g0126a0002c0003t0001g0104 | 3 | HG00642.hp1 HG02083.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.407-720_407-713del others(8): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083481 | |||||
| chrX:3083481
|
CCTATCTA others(5): Show |
C | 1 | a0001c0002t0001g0019 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.407-724_407-713del others(12): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083481 | |||||
| chrX:3083511
|
TATCTATC others(13): Show |
T | 1 | a0001c0001t0001g0180 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.407-728_407-709del others(20): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083511 | |||||
| chrX:3083515
|
TATCTATC others(9): Show |
T | 2 | a0001c0001t0001g0178a0005c0006t0001g0128 | 2 | HG01978.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.407-724_407-709del others(16): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083515 | |||||
| chrX:3083519
|
TATCTATC others(5): Show |
T | 28 | a0000c0018t0002g0129a0001c0001t0001g0002a0001c0001t0001g0008others(25): Show | 29 | HG00140.hp1 HG00673.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.407-720_407-709del others(12): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083519 | |||||
| chrX:3083523
|
TATCTATC others(1): Show |
T | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 111 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.407-716_407-709del others(8): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083523 | |||||
| chrX:3083527
|
TATCC | T | 18 | a0001c0001t0001g0036a0001c0001t0001g0050a0001c0001t0001g0061others(15): Show | 18 | HG01255.hp1 HG01258.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.407-698_407-695del others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083527 | |||||
| chrX:3083531
|
C | T | 5 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0085others(2): Show | 5 | NA18612.hp1 NA18971.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.407-712C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3083531 | ||||||
| chrX:3083851
|
C | T | 6 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.407-392C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3083851 | ||||||
| chrX:3083884
|
C | T | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.407-359C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3083884 | ||||||
| chrX:3084066
|
CA | C | 1 | a0001c0002t0001g0185 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.407-169delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3084066 | |||||
| chrX:3084079
|
G | A | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.407-164G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3084079 | ||||||
| chrX:3084178
|
T | C | 162 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(159): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.407-65T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3084178 | ||||||
| chrX:3084904
|
A | T | 1 | a0000c0014t0002g0022 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.830+238A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3084904 | ||||||
| chrX:3085097
|
C | T | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.830+431C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3085097 | ||||||
| chrX:3085120
|
T | C | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.830+454T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3085120 | ||||||
| chrX:3085217
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.830+551G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3085217 | ||||||
| chrX:3085261
|
G | A | 8 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(5): Show | 8 | HG02071.hp1 NA18612.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.830+595G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3085261 | ||||||
| chrX:3085302
|
G | GTA | 3 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037 | 3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.830+645_830+646dup others(2): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 3085302 | |||||
| chrX:3085360
|
A | T | 159 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(156): Show | 163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.830+694A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3085360 | ||||||
| chrX:3085541
|
T | C | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.830+875T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3085541 | ||||||
| chrX:3085646
|
AT | A | 3 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037 | 3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.830+986delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 3085646 | |||||
| chrX:3085853
|
A | T | 3 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037 | 3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.830+1187A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3085853 | ||||||
| chrX:3086020
|
T | TA | 3 | a0001c0001t0001g0164a0002c0004t0001g0087a0002c0004t0001g0181 | 3 | HG01071.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.830+1365dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 3086020 | |||||
| chrX:3086116
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0140 | 2 | HG01517.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.830+1450C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3086116 | ||||||
| chrX:3086580
|
G | T | 3 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037 | 3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.830+1914G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3086580 | ||||||
| chrX:3086602
|
G | A | 156 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(153): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.830+1936G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3086602 | ||||||
| chrX:3086627
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.830+1961G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3086627 | ||||||
| chrX:3086661
|
CA | C | 156 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(153): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.830+2002delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 3086661 | |||||
| chrX:3086817
|
T | C | 3 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037 | 3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.830+2151T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3086817 | ||||||
| chrX:3086824
|
T | TA | 3 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037 | 3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.830+2166dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 3086824 | |||||
| chrX:3086850
|
G | A | 1 | a0002c0003t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.830+2184G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3086850 | ||||||
| chrX:3087201
|
G | T | 162 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(159): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.831-2295G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3087201 | ||||||
| chrX:3087369
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0158others(1): Show | 4 | HG01168.hp2 HG01192.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.831-2127C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3087369 | ||||||
| chrX:3087636
|
G | T | 3 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037 | 3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.831-1860G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3087636 | ||||||
| chrX:3087649
|
A | T | 3 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037 | 3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.831-1847A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3087649 | ||||||
| chrX:3087703
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.831-1793G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3087703 | ||||||
| chrX:3087764
|
C | T | 3 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037 | 3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.831-1732C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3087764 | ||||||
| chrX:3087826
|
T | A | 1 | a0000c0014t0002g0022 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.831-1670T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3087826 | ||||||
| chrX:3087985
|
AT | A | 1 | a0001c0005t0001g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.831-1503delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 3087985 | |||||
| chrX:3088086
|
A | G | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.831-1410A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3088086 | ||||||
| chrX:3088209
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.831-1287G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3088209 | ||||||
| chrX:3088310
|
T | A | 1 | a0002c0003t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.831-1186T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3088310 | ||||||
| chrX:3088564
|
CT | C | 164 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(161): Show | 168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.831-917delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 3088564 | |||||
| chrX:3088564
|
CTT | C | 4 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0001g0093others(1): Show | 4 | HG01496.hp1 HG01515.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.831-918_831-917del others(2): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 3088564 | |||||
| chrX:3089162
|
A | G | 1 | a0006c0022t0001g0174 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.831-334A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3089162 | ||||||
| chrX:3089236
|
C | G | 7 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0186others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.831-260C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3089236 | ||||||
| chrX:3089439
|
G | T | 159 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(156): Show | 163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.831-57G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3089439 | ||||||
| chrX:3090231
|
T | C | 156 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(153): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.967+599T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3090231 | ||||||
| chrX:3090319
|
T | A | 159 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(156): Show | 163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.967+687T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3090319 | ||||||
| chrX:3090721
|
A | G | 3 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037 | 3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.967+1089A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3090721 | ||||||
| chrX:3090915
|
CTT | C | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.967+1295_967+1296d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3090915 | |||||
| chrX:3091047
|
GCTAT | G | 171 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(168): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.967+1420_967+1423d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3091047 | |||||
| chrX:3091061
|
C | A | 1 | a0001c0002t0001g0027 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.967+1429C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3091061 | ||||||
| chrX:3091578
|
C | A | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.967+1946C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3091578 | ||||||
| chrX:3091642
|
T | A | 3 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037 | 3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.967+2010T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3091642 | ||||||
| chrX:3091665
|
A | G | 3 | a0001c0001t0001g0134a0001c0001t0001g0137a0008c0019t0001g0076 | 3 | NA18944.hp1 NA18946.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.967+2033A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3091665 | ||||||
| chrX:3091823
|
T | TGATA | 169 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(166): Show | 173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.967+2193_967+2196d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3091823 | |||||
| chrX:3091833
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.967+2201T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3091833 | ||||||
| chrX:3091885
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.967+2253C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3091885 | ||||||
| chrX:3091938
|
CAG | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0158 | 2 | HG01168.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.967+2308_967+2309d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3091938 | |||||
| chrX:3092021
|
A | G | 3 | a0002c0004t0001g0087a0002c0004t0001g0181a0002c0004t0001g0182 | 3 | HG01070.hp1 HG01071.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.967+2389A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092021 | ||||||
| chrX:3092082
|
A | G | 2 | a0001c0005t0001g0007a0001c0005t0001g0009 | 2 | HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.967+2450A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092082 | ||||||
| chrX:3092167
|
T | TGATA | 6 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0187others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.967+2544_967+2547d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3092167 | |||||
| chrX:3092167
|
TGATA | T | 152 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(149): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.967+2544_967+2547d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3092167 | |||||
| chrX:3092172
|
GATAGATA others(5): Show |
G | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.967+2544_967+2555d others(14): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3092172 | |||||
| chrX:3092176
|
G | C | 4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0049others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.967+2544G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092176 | ||||||
| chrX:3092176
|
G | GATAC | 6 | a0001c0002t0001g0013a0002c0003t0001g0010a0002c0003t0001g0012others(3): Show | 6 | HG00597.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.967+2576_967+2579d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3092176 | |||||
| chrX:3092176
|
G | GATAGATA others(1): Show |
1 | a0001c0002t0001g0186 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.967+2547_967+2548i others(10): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3092176 | |||||
| chrX:3092180
|
C | CATAG | 1 | a0001c0016t0001g0156 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.967+2551_967+2552i others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3092180 | |||||
| chrX:3092180
|
C | G | 3 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037 | 3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.967+2548C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092180 | ||||||
| chrX:3092184
|
C | G | 3 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037 | 3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.967+2552C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092184 | ||||||
| chrX:3092212
|
G | C | 7 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0186others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.967+2580G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092212 | ||||||
| chrX:3092215
|
A | G | 156 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(153): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.967+2583A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092215 | ||||||
| chrX:3092371
|
C | G | 1 | a0001c0001t0001g0068 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.967+2739C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092371 | ||||||
| chrX:3092459
|
C | A | 162 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(159): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.967+2827C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092459 | ||||||
| chrX:3092622
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.967+2990A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092622 | ||||||
| chrX:3092653
|
G | T | 155 | a0000c0018t0002g0129a0001c0001t0001g0001a0001c0001t0001g0002others(152): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.967+3021G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092653 | ||||||
| chrX:3092835
|
T | C | 2 | a0001c0001t0001g0042a0002c0003t0001g0047 | 2 | HG03225.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.967+3203T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092835 | ||||||
| chrX:3092878
|
A | G | 3 | a0005c0006t0001g0005a0005c0006t0001g0006a0005c0006t0001g0128 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.967+3246A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092878 | ||||||
| chrX:3092894
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.967+3262C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092894 | ||||||
| chrX:3092901
|
G | A | 3 | a0001c0001t0001g0032a0001c0010t0001g0030a0001c0010t0001g0037 | 3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.967+3269G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092901 | ||||||
| chrX:3092971
|
A | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0161 | 2 | HG00609.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.967+3339A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092971 | ||||||
| chrX:3093003
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.967+3371T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093003 | ||||||
| chrX:3093012
|
T | A | 6 | a0000c0014t0002g0022a0001c0001t0001g0041a0001c0005t0001g0007others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.967+3380T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093012 | ||||||
| chrX:3093020
|
C | A | 7 | a0000c0014t0002g0022a0001c0001t0001g0041a0001c0005t0001g0007others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.967+3388C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093020 | ||||||
| chrX:3093022
|
C | A | 7 | a0000c0014t0002g0022a0001c0001t0001g0041a0001c0005t0001g0007others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.967+3390C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093022 | ||||||
| chrX:3093023
|
A | T | 7 | a0000c0014t0002g0022a0001c0001t0001g0041a0001c0005t0001g0007others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.967+3391A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093023 | ||||||
| chrX:3093024
|
T | TAGCTGG | 7 | a0000c0014t0002g0022a0001c0001t0001g0041a0001c0005t0001g0007others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.967+3392_967+3393i others(8): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093024 | ||||||
| chrX:3093025
|
C | G | 7 | a0000c0014t0002g0022a0001c0001t0001g0041a0001c0005t0001g0007others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.967+3393C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093025 | ||||||
| chrX:3093034
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0010t0001g0030others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+3402C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093034 | ||||||
| chrX:3093035
|
G | A | 1 | a0005c0006t0001g0128 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.967+3403G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093035 | ||||||
| chrX:3093040
|
T | C | 59 | a0000c0018t0002g0129a0001c0001t0001g0017a0001c0001t0001g0035others(56): Show | 59 | HG00597.hp1 HG00741.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.967+3408T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093040 | ||||||
| chrX:3093057
|
T | C | 10 | a0001c0001t0001g0069a0001c0002t0001g0013a0001c0012t0001g0086others(7): Show | 10 | HG00597.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.967+3425T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093057 | ||||||
| chrX:3093058
|
C | T | 10 | a0001c0001t0001g0069a0001c0002t0001g0013a0001c0012t0001g0086others(7): Show | 10 | HG00597.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.967+3426C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093058 | ||||||
| chrX:3093070
|
G | T | 4 | a0001c0002t0001g0184a0001c0002t0001g0185a0001c0002t0001g0186others(1): Show | 4 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.967+3438G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093070 | ||||||
| chrX:3093072
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.967+3440A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093072 | ||||||
| chrX:3093090
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.967+3458T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093090 | ||||||
| chrX:3093098
|
A | G | 6 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0164others(3): Show | 6 | HG00735.hp1 HG03041.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.967+3466A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093098 | ||||||
| chrX:3093110
|
G | GA | 2 | a0001c0001t0001g0072a0001c0001t0006g0064 | 2 | NA19056.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.967+3478_967+3479i others(3): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093110 | ||||||
| chrX:3093120
|
G | C | 1 | a0001c0001t0001g0155 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.967+3488G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093120 | ||||||
| chrX:3093144
|
A | G | 4 | a0000c0018t0002g0129a0001c0007t0003g0028a0001c0007t0003g0183others(1): Show | 4 | HG02257.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+3512A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093144 | ||||||
| chrX:3093147
|
G | A | 4 | a0000c0018t0002g0129a0001c0007t0003g0028a0001c0007t0003g0183others(1): Show | 4 | HG02257.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+3515G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093147 | ||||||
| chrX:3093151
|
C | T | 17 | a0001c0001t0001g0032a0001c0001t0001g0069a0001c0002t0001g0013others(14): Show | 17 | HG00099.hp2 HG00597.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.967+3519C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093151 | ||||||
| chrX:3093152
|
G | A | 4 | a0000c0018t0002g0129a0001c0007t0003g0028a0001c0007t0003g0183others(1): Show | 4 | HG02257.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+3520G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093152 | ||||||
| chrX:3093159
|
C | T | 4 | a0001c0001t0001g0049a0001c0001t0001g0095a0001c0001t0001g0145others(1): Show | 4 | HG02040.hp1 NA18948.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+3527C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093159 | ||||||
| chrX:3093160
|
G | A | 4 | a0000c0018t0002g0129a0001c0007t0003g0028a0001c0007t0003g0183others(1): Show | 4 | HG02257.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+3528G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093160 | ||||||
| chrX:3093169
|
GA | G | 3 | a0002c0004t0001g0087a0002c0004t0001g0181a0002c0004t0001g0182 | 3 | HG01070.hp1 HG01071.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.967+3546delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3093169 | |||||
| chrX:3093292
|
G | A | 45 | a0000c0018t0002g0129a0001c0001t0001g0035a0001c0001t0001g0036others(42): Show | 45 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.967+3660G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093292 | ||||||
| chrX:3093313
|
GT | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0180 | 2 | HG02132.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.967+3682delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093313 | ||||||
| chrX:3093678
|
T | A | 1 | a0001c0012t0001g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.967+4046T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093678 | ||||||
| chrX:3093681
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0158others(1): Show | 4 | HG01168.hp2 HG01192.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+4049G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093681 | ||||||
| chrX:3093686
|
G | C | 9 | a0001c0001t0001g0032a0001c0015t0007g0018a0001c0020t0001g0092others(6): Show | 9 | HG01070.hp1 HG01071.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.967+4054G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093686 | ||||||
| chrX:3093709
|
G | A | 5 | a0001c0015t0007g0018a0001c0020t0001g0092a0005c0006t0001g0005others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.967+4077G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093709 | ||||||
| chrX:3093710
|
T | G | 26 | a0000c0018t0002g0129a0001c0001t0001g0032a0001c0002t0001g0019others(23): Show | 26 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.967+4078T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093710 | ||||||
| chrX:3093742
|
G | A | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.967+4110G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093742 | ||||||
| chrX:3093839
|
A | C | 13 | a0000c0018t0002g0129a0001c0002t0001g0019a0001c0002t0001g0065others(10): Show | 13 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.967+4207A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093839 | ||||||
| chrX:3093906
|
CT | C | 1 | a0001c0001t0001g0175 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.967+4278delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3093906 | |||||
| chrX:3093926
|
TG | T | 1 | a0001c0001t0001g0175 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.967+4297delG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3093926 | |||||
| chrX:3093927
|
G | C | 1 | a0001c0001t0001g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.967+4295G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093927 | ||||||
| chrX:3094020
|
C | G | 4 | a0001c0005t0001g0039a0001c0005t0001g0040a0001c0016t0001g0156others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.967+4388C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094020 | ||||||
| chrX:3094177
|
T | C | 11 | a0001c0005t0001g0007a0001c0005t0001g0009a0001c0005t0001g0039others(8): Show | 11 | HG01168.hp1 HG01169.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.967+4545T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094177 | ||||||
| chrX:3094201
|
G | C | 4 | a0001c0001t0001g0032a0002c0004t0001g0087a0002c0004t0001g0181others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+4569G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094201 | ||||||
| chrX:3094364
|
A | G | 26 | a0000c0018t0002g0129a0001c0001t0001g0032a0001c0002t0001g0019others(23): Show | 26 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.967+4732A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094364 | ||||||
| chrX:3094368
|
G | A | 2 | a0001c0005t0001g0007a0001c0005t0001g0009 | 2 | HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.967+4736G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094368 | ||||||
| chrX:3094552
|
C | T | 4 | a0001c0007t0003g0028a0001c0007t0003g0183a0001c0010t0001g0030others(1): Show | 4 | HG02257.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+4920C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094552 | ||||||
| chrX:3094578
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.967+4946A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094578 | ||||||
| chrX:3094596
|
T | C | 4 | a0001c0007t0003g0028a0001c0007t0003g0183a0001c0010t0001g0030others(1): Show | 4 | HG02257.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+4964T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094596 | ||||||
| chrX:3094752
|
T | C | 4 | a0001c0007t0003g0028a0001c0007t0003g0183a0001c0010t0001g0030others(1): Show | 4 | HG02257.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+5120T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094752 | ||||||
| chrX:3094991
|
T | G | 13 | a0000c0018t0002g0129a0001c0002t0001g0019a0001c0002t0001g0065others(10): Show | 13 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.967+5359T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094991 | ||||||
| chrX:3095042
|
G | A | 1 | a0001c0002t0001g0026 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.967+5410G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3095042 | ||||||
| chrX:3095138
|
A | C | 11 | a0001c0001t0001g0083a0001c0002t0001g0019a0001c0002t0001g0065others(8): Show | 11 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.967+5506A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3095138 | ||||||
| chrX:3095346
|
A | G | 29 | a0000c0018t0002g0129a0001c0001t0001g0032a0001c0001t0001g0083others(26): Show | 29 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.967+5714A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3095346 | ||||||
| chrX:3095741
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.968-5346A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3095741 | ||||||
| chrX:3095772
|
G | A | 14 | a0000c0018t0002g0129a0001c0001t0001g0083a0001c0002t0001g0019others(11): Show | 14 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-5315G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3095772 | ||||||
| chrX:3095879
|
T | A | 4 | a0001c0001t0001g0032a0002c0004t0001g0087a0002c0004t0001g0181others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.968-5208T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3095879 | ||||||
| chrX:3095881
|
T | C | 43 | a0000c0018t0002g0129a0001c0001t0001g0032a0001c0001t0001g0048others(40): Show | 43 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.968-5206T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3095881 | ||||||
| chrX:3095951
|
CT | C | 11 | a0001c0005t0001g0007a0001c0005t0001g0009a0001c0005t0001g0039others(8): Show | 11 | HG01168.hp1 HG01169.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.968-5135delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3095951 | ||||||
| chrX:3096023
|
G | A | 17 | a0000c0018t0002g0129a0001c0001t0001g0032a0001c0002t0001g0019others(14): Show | 17 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.968-5064G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3096023 | ||||||
| chrX:3096586
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.968-4501A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3096586 | ||||||
| chrX:3096816
|
TC | T | 13 | a0000c0018t0002g0129a0001c0002t0001g0019a0001c0002t0001g0065others(10): Show | 13 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.968-4265delC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3096816 | |||||
| chrX:3096977
|
G | A | 4 | a0001c0007t0003g0028a0001c0007t0003g0183a0001c0010t0001g0030others(1): Show | 4 | HG02257.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.968-4110G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3096977 | ||||||
| chrX:3097030
|
TC | T | 2 | a0004c0011t0001g0024a0004c0011t0001g0031 | 2 | HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.968-4055delC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3097030 | |||||
| chrX:3097481
|
A | C | 1 | a0003c0008t0001g0115 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.968-3606A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3097481 | ||||||
| chrX:3097907
|
G | A | 4 | a0001c0007t0003g0028a0001c0007t0003g0183a0001c0010t0001g0030others(1): Show | 4 | HG02257.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.968-3180G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3097907 | ||||||
| chrX:3098020
|
A | AAT | 16 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(13): Show | 17 | HG00738.hp1 HG01256.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.968-3055_968-3054d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098020 | |||||
| chrX:3098020
|
A | AATAT | 5 | a0001c0015t0007g0018a0001c0020t0001g0092a0005c0006t0001g0005others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.968-3057_968-3054d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098020 | |||||
| chrX:3098047
|
A | AAC | 14 | a0001c0001t0001g0029a0001c0001t0001g0048a0001c0001t0001g0050others(11): Show | 14 | HG01099.hp1 HG01109.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-3000_968-2999d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098047 | |||||
| chrX:3098047
|
A | AACAC | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(83): Show | 89 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.968-3002_968-2999d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098047 | |||||
| chrX:3098047
|
A | AACACAC | 30 | a0000c0014t0002g0022a0000c0018t0002g0129a0001c0001t0001g0016others(27): Show | 30 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.968-3004_968-2999d others(8): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098047 | |||||
| chrX:3098047
|
A | AACACACA others(1): Show |
20 | a0001c0001t0001g0017a0001c0001t0001g0099a0001c0001t0001g0135others(17): Show | 20 | HG00597.hp2 HG00741.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.968-3006_968-2999d others(10): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098047 | |||||
| chrX:3098047
|
A | AACACACA others(3): Show |
7 | a0001c0001t0001g0077a0001c0001t0001g0140a0001c0001t0001g0145others(4): Show | 7 | HG02257.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.968-3008_968-2999d others(12): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098047 | |||||
| chrX:3098047
|
A | AACACACA others(5): Show |
1 | a0001c0001t0001g0133 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.968-3010_968-2999d others(14): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098047 | |||||
| chrX:3098047
|
AAC | A | 2 | a0001c0001t0001g0161a0002c0003t0001g0047 | 2 | HG00609.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.968-3000_968-2999d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098047 | |||||
| chrX:3098047
|
AACAC | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0044others(8): Show | 12 | HG00738.hp1 HG01952.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.968-3002_968-2999d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098047 | |||||
| chrX:3098047
|
AACACAC | A | 5 | a0001c0001t0001g0032a0001c0001t0001g0045a0002c0004t0001g0087others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.968-3004_968-2999d others(8): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098047 | |||||
| chrX:3098131
|
A | T | 1 | a0002c0004t0001g0127 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.968-2956A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3098131 | ||||||
| chrX:3098355
|
T | TAG | 13 | a0000c0018t0002g0129a0001c0002t0001g0019a0001c0002t0001g0065others(10): Show | 13 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.968-2720_968-2719d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098355 | |||||
| chrX:3098523
|
G | C | 6 | a0001c0005t0001g0007a0001c0005t0001g0009a0001c0005t0001g0039others(3): Show | 6 | HG02280.hp2 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.968-2564G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3098523 | ||||||
| chrX:3098610
|
G | A | 4 | a0001c0007t0003g0028a0001c0007t0003g0183a0001c0010t0001g0030others(1): Show | 4 | HG02257.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.968-2477G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3098610 | ||||||
| chrX:3098657
|
G | A | 1 | a0001c0002t0001g0023 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.968-2430G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3098657 | ||||||
| chrX:3098796
|
AT | A | 1 | a0001c0001t0001g0053 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.968-2289delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098796 | |||||
| chrX:3098833
|
A | AT | 1 | a0001c0001t0001g0085 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.968-2247dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098833 | |||||
| chrX:3098841
|
G | A | 4 | a0001c0001t0001g0032a0002c0004t0001g0087a0002c0004t0001g0181others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.968-2246G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3098841 | ||||||
| chrX:3098874
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.968-2213A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3098874 | ||||||
| chrX:3099003
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.968-2084T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3099003 | ||||||
| chrX:3099014
|
G | A | 1 | a0001c0001t0005g0112 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.968-2073G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3099014 | ||||||
| chrX:3099029
|
T | C | 28 | a0000c0018t0002g0129a0001c0001t0001g0032a0001c0002t0001g0019others(25): Show | 28 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.968-2058T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3099029 | ||||||
| chrX:3099317
|
C | T | 1 | a0001c0002t0001g0065 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.968-1770C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3099317 | ||||||
| chrX:3099408
|
C | T | 4 | a0001c0007t0003g0028a0001c0007t0003g0183a0001c0010t0001g0030others(1): Show | 4 | HG02257.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.968-1679C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3099408 | ||||||
| chrX:3099429
|
C | A | 1 | a0001c0002t0001g0027 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.968-1658C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3099429 | ||||||
| chrX:3099476
|
A | G | 1 | a0001c0002t0001g0019 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.968-1611A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3099476 | ||||||
| chrX:3100534
|
A | AT | 1 | a0001c0001t0001g0085 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.968-546dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3100534 | |||||
| chrX:3100587
|
G | GTTTTTTG others(1): Show |
17 | a0000c0018t0002g0129a0001c0001t0001g0032a0001c0002t0001g0019others(14): Show | 17 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.968-486_968-479dup others(8): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3100587 | |||||
| chrX:3100644
|
T | C | 45 | a0000c0018t0002g0129a0001c0001t0001g0032a0001c0001t0001g0035others(42): Show | 45 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.968-443T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3100644 | ||||||
| chrX:3100690
|
C | T | 1 | a0002c0003t0001g0146 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.968-397C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3100690 | ||||||
| chrX:3100884
|
C | G | 17 | a0000c0018t0002g0129a0001c0001t0001g0032a0001c0002t0001g0019others(14): Show | 17 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.968-203C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3100884 | ||||||
| chrX:3101073
|
G | A | 13 | a0000c0018t0002g0129a0001c0002t0001g0019a0001c0002t0001g0065others(10): Show | 13 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.968-14G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3101073 | ||||||
| chrX:3101424
|
T | G | 32 | a0000c0018t0002g0129a0001c0001t0001g0032a0001c0002t0001g0019others(29): Show | 32 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.1102+203T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3101424 | ||||||
| chrX:3101833
|
A | G | 12 | a0000c0018t0002g0129a0001c0002t0001g0019a0001c0002t0001g0065others(9): Show | 12 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1102+612A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3101833 | ||||||
| chrX:3101961
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1102+740C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3101961 | ||||||
| chrX:3102046
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1102+825T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102046 | ||||||
| chrX:3102135
|
T | A | 13 | a0000c0018t0002g0129a0001c0002t0001g0019a0001c0002t0001g0065others(10): Show | 13 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1102+914T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102135 | ||||||
| chrX:3102195
|
T | C | 13 | a0000c0018t0002g0129a0001c0002t0001g0019a0001c0002t0001g0065others(10): Show | 13 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1102+974T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102195 | ||||||
| chrX:3102257
|
T | C | 5 | a0001c0015t0007g0018a0001c0020t0001g0092a0005c0006t0001g0005others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1102+1036T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102257 | ||||||
| chrX:3102308
|
A | G | 17 | a0000c0018t0002g0129a0001c0002t0001g0019a0001c0002t0001g0065others(14): Show | 17 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1102+1087A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102308 | ||||||
| chrX:3102493
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1103-1269G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102493 | ||||||
| chrX:3102500
|
C | T | 1 | a0002c0003t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1103-1262C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102500 | ||||||
| chrX:3102594
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0140 | 2 | HG01517.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1103-1168C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102594 | ||||||
| chrX:3102617
|
G | A | 4 | a0001c0001t0001g0032a0002c0004t0001g0087a0002c0004t0001g0181others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1103-1145G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102617 | ||||||
| chrX:3102765
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1103-997A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102765 | ||||||
| chrX:3102799
|
C | G | 4 | a0001c0005t0001g0039a0001c0005t0001g0040a0001c0016t0001g0156others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1103-963C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102799 | ||||||
| chrX:3102809
|
G | A | 13 | a0000c0018t0002g0129a0001c0002t0001g0019a0001c0002t0001g0065others(10): Show | 13 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1103-953G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102809 | ||||||
| chrX:3102826
|
G | C | 41 | a0000c0018t0002g0129a0001c0001t0001g0032a0001c0001t0001g0048others(38): Show | 41 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1103-936G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102826 | ||||||
| chrX:3102827
|
G | A | 41 | a0000c0018t0002g0129a0001c0001t0001g0032a0001c0001t0001g0048others(38): Show | 41 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1103-935G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102827 | ||||||
| chrX:3102829
|
G | T | 41 | a0000c0018t0002g0129a0001c0001t0001g0032a0001c0001t0001g0048others(38): Show | 41 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1103-933G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102829 | ||||||
| chrX:3102860
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1103-902C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102860 | ||||||
| chrX:3102862
|
C | A | 1 | a0001c0001t0001g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1103-900C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102862 | ||||||
| chrX:3102869
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(4): Show | 8 | HG00738.hp1 HG01256.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1103-893A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102869 | ||||||
| chrX:3102886
|
T | TG | 1 | a0001c0001t0001g0110 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1103-874dupG | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 3102886 | |||||
| chrX:3102890
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1103-872A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102890 | ||||||
| chrX:3102898
|
G | C | 1 | a0001c0001t0001g0110 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1103-864G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102898 | ||||||
| chrX:3102906
|
A | G | 5 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0001g0123others(2): Show | 5 | NA18945.hp1 NA18951.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1103-856A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102906 | ||||||
| chrX:3102910
|
C | CA | 12 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0062others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1103-839dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 3102910 | |||||
| chrX:3102940
|
C | T | 2 | a0001c0010t0001g0030a0001c0010t0001g0037 | 2 | HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1103-822C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102940 | ||||||
| chrX:3103067
|
TA | T | 5 | a0001c0015t0007g0018a0001c0020t0001g0092a0005c0006t0001g0005others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1103-693delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 3103067 | |||||
| chrX:3103104
|
G | C | 1 | a0001c0001t0001g0108 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1103-658G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3103104 | ||||||
| chrX:3103194
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1103-568C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3103194 | ||||||
| chrX:3103339
|
A | T | 1 | a0002c0004t0001g0127 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1103-423A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3103339 | ||||||
| chrX:3103355
|
C | T | 1 | a0001c0012t0001g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1103-407C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3103355 | ||||||
| chrX:3103474
|
G | A | 4 | a0001c0001t0001g0032a0002c0004t0001g0087a0002c0004t0001g0181others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1103-288G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3103474 | ||||||
| chrX:3103612
|
C | T | 4 | a0001c0001t0001g0032a0002c0004t0001g0087a0002c0004t0001g0181others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1103-150C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3103612 | ||||||
| chrX:3103757
|
T | C | 13 | a0000c0018t0002g0129a0001c0002t0001g0019a0001c0002t0001g0065others(10): Show | 13 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.1103-5T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3103757 | ||||||
| chrX:3104626
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1265+702G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3104626 | ||||||
| chrX:3104677
|
G | A | 2 | a0002c0003t0001g0010a0002c0003t0001g0012 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1265+753G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3104677 | ||||||
| chrX:3104733
|
G | C | 1 | a0002c0003t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1265+809G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3104733 | ||||||
| chrX:3104877
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1265+953T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3104877 | ||||||
| chrX:3105007
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1265+1083G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3105007 | ||||||
| chrX:3105266
|
A | G | 17 | a0000c0018t0002g0129a0001c0001t0001g0032a0001c0002t0001g0019others(14): Show | 17 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.1265+1342A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3105266 | ||||||
| chrX:3105324
|
C | G | 30 | a0000c0018t0002g0129a0001c0001t0001g0032a0001c0002t0001g0019others(27): Show | 30 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1265+1400C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3105324 | ||||||
| chrX:3105429
|
C | A | 1 | a0001c0012t0001g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1265+1505C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3105429 | ||||||
| chrX:3105430
|
T | A | 1 | a0001c0012t0001g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1265+1506T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3105430 | ||||||
| chrX:3105467
|
T | C | 2 | a0001c0009t0001g0014a0001c0009t0001g0015 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1265+1543T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3105467 | ||||||
| chrX:3105496
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1265+1572G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3105496 | ||||||
| chrX:3105600
|
G | C | 1 | a0002c0003t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1265+1676G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3105600 | ||||||
| chrX:3106277
|
T | A | 6 | a0001c0005t0001g0007a0001c0005t0001g0009a0001c0005t0001g0039others(3): Show | 6 | HG02280.hp2 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1265+2353T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3106277 | ||||||
| chrX:3106281
|
G | A | 1 | a0003c0017t0001g0139 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1265+2357G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3106281 | ||||||
| chrX:3106324
|
A | G | 1 | a0002c0003t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1265+2400A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3106324 | ||||||
| chrX:3106343
|
C | T | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1265+2419C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3106343 | ||||||
| chrX:3106385
|
A | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0061a0001c0001t0001g0175 | 4 | NA18951.hp1 NA18986.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1265+2461A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3106385 | ||||||
| chrX:3106511
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1265+2587T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3106511 | ||||||
| chrX:3107006
|
T | C | 1 | a0004c0023t0001g0169 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1265+3082T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107006 | ||||||
| chrX:3107133
|
A | G | 21 | a0000c0018t0002g0129a0001c0001t0001g0032a0001c0002t0001g0019others(18): Show | 21 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.1266-2995A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107133 | ||||||
| chrX:3107368
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0093 | 3 | HG00735.hp2 HG01070.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1266-2760C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107368 | ||||||
| chrX:3107433
|
G | C | 19 | a0001c0001t0001g0032a0001c0005t0001g0007a0001c0005t0001g0009others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1266-2695G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107433 | ||||||
| chrX:3107547
|
A | G | 19 | a0001c0001t0001g0032a0001c0005t0001g0007a0001c0005t0001g0009others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1266-2581A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107547 | ||||||
| chrX:3107647
|
G | A | 2 | a0001c0007t0003g0028a0001c0007t0003g0183 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1266-2481G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107647 | ||||||
| chrX:3107675
|
G | C | 4 | a0001c0001t0001g0032a0002c0004t0001g0087a0002c0004t0001g0181others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266-2453G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107675 | ||||||
| chrX:3107696
|
A | AC | 43 | a0000c0018t0002g0129a0001c0001t0001g0032a0001c0001t0001g0048others(40): Show | 43 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.1266-2432_1266-243 others(5): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107696 | ||||||
| chrX:3107732
|
C | A | 19 | a0001c0001t0001g0032a0001c0005t0001g0007a0001c0005t0001g0009others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1266-2396C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107732 | ||||||
| chrX:3107737
|
T | C | 19 | a0001c0001t0001g0032a0001c0005t0001g0007a0001c0005t0001g0009others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1266-2391T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107737 | ||||||
| chrX:3108105
|
G | T | 4 | a0003c0008t0001g0115a0003c0008t0001g0167a0003c0013t0001g0096others(1): Show | 4 | HG01074.hp1 HG02258.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266-2023G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3108105 | ||||||
| chrX:3108697
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1266-1431T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3108697 | ||||||
| chrX:3108822
|
GC | G | 1 | a0001c0001t0001g0053 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1266-1304delC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 3108822 | |||||
| chrX:3108945
|
G | A | 4 | a0001c0002t0001g0019a0001c0002t0001g0065a0001c0009t0001g0014others(1): Show | 4 | HG03491.hp1 HG03492.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266-1183G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3108945 | ||||||
| chrX:3109063
|
TA | T | 1 | a0001c0001t0001g0053 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1266-1063delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 3109063 | |||||
| chrX:3109079
|
A | G | 15 | a0001c0005t0001g0007a0001c0005t0001g0009a0001c0005t0001g0039others(12): Show | 15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1266-1049A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3109079 | ||||||
| chrX:3109144
|
AC | A | 1 | a0001c0001t0001g0053 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1266-980delC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 3109144 | |||||
| chrX:3109171
|
T | C | 15 | a0001c0005t0001g0007a0001c0005t0001g0009a0001c0005t0001g0039others(12): Show | 15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1266-957T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3109171 | ||||||
| chrX:3109211
|
T | C | 20 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0005t0001g0007others(17): Show | 20 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1266-917T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3109211 | ||||||
| chrX:3109286
|
CT | C | 15 | a0001c0005t0001g0007a0001c0005t0001g0009a0001c0005t0001g0039others(12): Show | 15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1266-841delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3109286 | ||||||
| chrX:3109288
|
C | T | 1 | a0002c0003t0001g0146 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1266-840C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3109288 | ||||||
| chrX:3109554
|
G | A | 4 | a0003c0008t0001g0115a0003c0008t0001g0167a0003c0013t0001g0096others(1): Show | 4 | HG01074.hp1 HG02258.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266-574G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3109554 | ||||||
| chrX:3109707
|
C | T | 1 | a0002c0003t0001g0146 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1266-421C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3109707 | ||||||
| chrX:3110013
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1266-115G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3110013 | ||||||
| chrX:3110344
|
G | A | 13 | a0001c0005t0001g0039a0001c0005t0001g0040a0001c0015t0007g0018others(10): Show | 13 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1390+92G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3110344 | ||||||
| chrX:3110364
|
C | T | 15 | a0001c0005t0001g0007a0001c0005t0001g0009a0001c0005t0001g0039others(12): Show | 15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1390+112C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3110364 | ||||||
| chrX:3110471
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0154 | 2 | NA18959.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1390+219G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3110471 | ||||||
| chrX:3110586
|
A | G | 15 | a0001c0005t0001g0007a0001c0005t0001g0009a0001c0005t0001g0039others(12): Show | 15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1390+334A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3110586 | ||||||
| chrX:3111077
|
C | T | 35 | a0000c0018t0002g0129a0001c0002t0001g0019a0001c0002t0001g0065others(32): Show | 35 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1390+825C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111077 | ||||||
| chrX:3111125
|
GCTTT | G | 5 | a0001c0015t0007g0018a0001c0020t0001g0092a0005c0006t0001g0005others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1390+886_1390+889d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 3111125 | |||||
| chrX:3111138
|
C | CT | 1 | a0000c0018t0002g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1390+900dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 3111138 | |||||
| chrX:3111138
|
CT | C | 8 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(5): Show | 8 | HG02071.hp1 NA18612.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390+900delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 3111138 | |||||
| chrX:3111193
|
G | GT | 1 | a0008c0019t0001g0076 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1390+943dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 3111193 | |||||
| chrX:3111232
|
T | G | 1 | a0002c0003t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1391-942T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111232 | ||||||
| chrX:3111307
|
C | A | 15 | a0001c0005t0001g0007a0001c0005t0001g0009a0001c0005t0001g0039others(12): Show | 15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1391-867C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111307 | ||||||
| chrX:3111308
|
C | A | 6 | a0002c0003t0001g0010a0002c0003t0001g0012a0002c0003t0001g0104others(3): Show | 6 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1391-866C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111308 | ||||||
| chrX:3111335
|
TA | T | 1 | a0008c0019t0001g0076 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1391-834delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 3111335 | |||||
| chrX:3111344
|
G | A | 35 | a0000c0018t0002g0129a0001c0002t0001g0019a0001c0002t0001g0065others(32): Show | 35 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1391-830G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111344 | ||||||
| chrX:3111412
|
G | A | 6 | a0001c0005t0001g0007a0001c0005t0001g0009a0001c0005t0001g0039others(3): Show | 6 | HG02280.hp2 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1391-762G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111412 | ||||||
| chrX:3111440
|
T | C | 17 | a0000c0018t0002g0129a0001c0002t0001g0019a0001c0002t0001g0065others(14): Show | 17 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1391-734T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111440 | ||||||
| chrX:3111466
|
C | A | 6 | a0001c0005t0001g0007a0001c0005t0001g0009a0001c0005t0001g0039others(3): Show | 6 | HG02280.hp2 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1391-708C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111466 | ||||||
| chrX:3111590
|
AC | A | 1 | a0008c0019t0001g0076 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1391-582delC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 3111590 | |||||
| chrX:3111698
|
A | G | 1 | a0000c0018t0002g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1391-476A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111698 | ||||||
| chrX:3111702
|
T | C | 15 | a0001c0005t0001g0007a0001c0005t0001g0009a0001c0005t0001g0039others(12): Show | 15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1391-472T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111702 | ||||||
| chrX:3111847
|
G | A | 1 | a0001c0005t0001g0007 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1391-327G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111847 | ||||||
| chrX:3111964
|
C | T | 15 | a0001c0005t0001g0007a0001c0005t0001g0009a0001c0005t0001g0039others(12): Show | 15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1391-210C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111964 | ||||||
| chrX:3112140
|
G | A | 8 | a0001c0005t0001g0040a0001c0015t0007g0018a0001c0016t0001g0156others(5): Show | 8 | HG01168.hp1 HG01169.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1391-34G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3112140 |