| geneid | 7499 |
|---|---|
| ensemblid | ENSG00000124343.14 |
| hgncid | 12806 |
| symbol | XG |
| name | Xg glycoprotein (Xg blood group) |
| refseq_nuc | NM_001141919.2 |
| refseq_prot | NP_001135391.1 |
| ensembl_nuc | ENST00000644266.2 |
| ensembl_prot | ENSP00000494087.1 |
| mane_status | MANE Select |
| chr | chrX |
| start | 2752040 |
| end | 2816500 |
| strand | + |
| ver | v1.2 |
| region | chrX:2752040-2816500 |
| region5000 | chrX:2747040-2821500 |
| regionname0 | XG_chrX_2752040_2816500 |
| regionname5000 | XG_chrX_2747040_2821500 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 195 | 300 | 71 | 49 | 142 | 9 | 29 | 109 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0002 | 1/0 | 195 | 13 | 7 | 4 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0003 | 0/1 | 195 | 7 | 0 | 2 | 0 | 4 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0004 | 0/0 | 195 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0005 | 0/0 | 129 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 588 | 281 | 53 | 49 | 142 | 9 | 28 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| c0002 | 0/0 | 588 | 16 | 16 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| c0003 | 1/0 | 588 | 12 | 6 | 4 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| c0004 | 0/1 | 588 | 7 | 0 | 2 | 0 | 4 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| c0005 | 0/0 | 588 | 2 | 2 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| c0006 | 0/0 | 589 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| c0007 | 0/0 | 588 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| c0008 | 0/0 | 588 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| c0009 | 0/0 | 588 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2372 | 105 | 16 | 14 | 55 | 7 | 13 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0002 | 0/1 | 2370 | 40 | 0 | 19 | 13 | 4 | 3 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0003 | 0/0 | 2368 | 38 | 6 | 5 | 24 | 0 | 3 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0004 | 0/0 | 2372 | 22 | 0 | 0 | 22 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0005 | 0/0 | 2366 | 18 | 15 | 2 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0006 | 0/0 | 2366 | 11 | 0 | 1 | 9 | 0 | 1 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0007 | 0/0 | 2354 | 7 | 7 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0008 | 0/0 | 2356 | 7 | 6 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0009 | 0/0 | 2374 | 5 | 0 | 1 | 2 | 2 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0010 | 0/0 | 2368 | 4 | 2 | 1 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0011 | 0/0 | 2360 | 4 | 0 | 3 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0012 | 0/0 | 2358 | 3 | 2 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0013 | 0/0 | 2370 | 3 | 3 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0014 | 0/0 | 2368 | 3 | 0 | 0 | 0 | 0 | 3 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0015 | 0/0 | 2370 | 3 | 2 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0016 | 0/0 | 2368 | 3 | 0 | 0 | 1 | 0 | 2 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0017 | 0/0 | 2362 | 3 | 0 | 0 | 3 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0018 | 0/0 | 2362 | 2 | 0 | 0 | 2 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0019 | 0/0 | 2370 | 2 | 1 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0020 | 0/0 | 2366 | 2 | 2 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0021 | 0/0 | 2368 | 2 | 2 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0022 | 0/0 | 2354 | 2 | 2 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0023 | 0/0 | 2376 | 2 | 0 | 2 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0024 | 0/0 | 2372 | 2 | 0 | 0 | 1 | 0 | 1 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0025 | 0/0 | 2366 | 2 | 2 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0026 | 0/0 | 2372 | 2 | 0 | 0 | 2 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0027 | 1/0 | 2356 | 2 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0028 | 0/0 | 2366 | 2 | 0 | 0 | 2 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0029 | 0/0 | 2372 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0030 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0031 | 0/0 | 2376 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0032 | 0/0 | 2364 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0033 | 0/0 | 2372 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0034 | 0/0 | 2366 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0035 | 0/0 | 2372 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0036 | 0/0 | 2366 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0037 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0038 | 0/0 | 2374 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0039 | 0/0 | 2372 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0040 | 0/0 | 2372 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0041 | 0/0 | 2366 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0042 | 0/0 | 2378 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0043 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0044 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0045 | 0/0 | 2370 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0046 | 0/0 | 2370 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0047 | 0/0 | 2366 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0048 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| t0049 | 0/0 | 2372 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0235 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0248 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 588 | 281 | 53 | 49 | 142 | 9 | 28 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0002 | 0/0 | 588 | 16 | 16 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0005 | 0/0 | 588 | 2 | 2 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0007 | 0/0 | 588 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0002c0003 | 1/0 | 588 | 12 | 6 | 4 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0002c0008 | 0/0 | 588 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0003c0004 | 0/1 | 588 | 7 | 0 | 2 | 0 | 4 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0004c0009 | 0/0 | 588 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0005c0006 | 0/0 | 589 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2959 | 98 | 13 | 13 | 53 | 6 | 13 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0002 | 0/0 | 2957 | 37 | 0 | 18 | 13 | 3 | 3 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0003 | 0/0 | 2955 | 38 | 6 | 5 | 24 | 0 | 3 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0004 | 0/0 | 2959 | 22 | 0 | 0 | 22 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0005 | 0/0 | 2953 | 14 | 11 | 2 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0006 | 0/0 | 2953 | 11 | 0 | 1 | 9 | 0 | 1 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0007 | 0/0 | 2941 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0008 | 0/0 | 2943 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0009 | 0/0 | 2961 | 3 | 0 | 1 | 2 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0010 | 0/0 | 2955 | 4 | 2 | 1 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0011 | 0/0 | 2947 | 4 | 0 | 3 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0012 | 0/0 | 2945 | 2 | 1 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0013 | 0/0 | 2957 | 3 | 3 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0014 | 0/0 | 2955 | 3 | 0 | 0 | 0 | 0 | 3 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0015 | 0/0 | 2957 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0016 | 0/0 | 2955 | 3 | 0 | 0 | 1 | 0 | 2 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0017 | 0/0 | 2949 | 3 | 0 | 0 | 3 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0018 | 0/0 | 2949 | 2 | 0 | 0 | 2 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0019 | 0/0 | 2957 | 2 | 1 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0020 | 0/0 | 2953 | 2 | 2 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0021 | 0/0 | 2955 | 2 | 2 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0022 | 0/0 | 2941 | 2 | 2 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0023 | 0/0 | 2963 | 2 | 0 | 2 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0024 | 0/0 | 2959 | 2 | 0 | 0 | 1 | 0 | 1 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0025 | 0/0 | 2953 | 2 | 2 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0026 | 0/0 | 2959 | 2 | 0 | 0 | 2 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0027 | 0/0 | 2943 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0028 | 0/0 | 2953 | 2 | 0 | 0 | 2 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0029 | 0/0 | 2959 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0030 | 0/0 | 2951 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0033 | 0/0 | 2959 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0036 | 0/0 | 2953 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0038 | 0/0 | 2961 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0039 | 0/0 | 2959 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0042 | 0/0 | 2965 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0043 | 0/0 | 2954 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0046 | 0/0 | 2957 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0047 | 0/0 | 2953 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0048 | 0/0 | 2945 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0001t0049 | 0/0 | 2959 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0002t0001 | 0/0 | 2959 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0002t0005 | 0/0 | 2953 | 4 | 4 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0002t0007 | 0/0 | 2941 | 5 | 5 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0002t0008 | 0/0 | 2943 | 2 | 2 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0002t0012 | 0/0 | 2945 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0002t0034 | 0/0 | 2953 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0002t0041 | 0/0 | 2953 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0002t0044 | 0/0 | 2945 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0005t0015 | 0/0 | 2957 | 2 | 2 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0001c0007t0032 | 0/0 | 2951 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0002c0003t0001 | 0/0 | 2959 | 3 | 2 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0002c0003t0007 | 0/0 | 2941 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0002c0003t0008 | 0/0 | 2943 | 4 | 3 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0002c0003t0027 | 1/0 | 2943 | 1 | 0 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0002c0003t0031 | 0/0 | 2963 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0002c0003t0040 | 0/0 | 2959 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0002c0003t0045 | 0/0 | 2957 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0002c0008t0037 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0003c0004t0001 | 0/0 | 2959 | 2 | 0 | 1 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0003c0004t0002 | 0/1 | 2957 | 3 | 0 | 1 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0003c0004t0009 | 0/0 | 2961 | 2 | 0 | 0 | 0 | 2 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0004c0009t0035 | 0/0 | 2959 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| a0005c0006t0001 | 0/0 | 2960 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | copy fasta | chrX | 2747040 | 2821500 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0005g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0005g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0006g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0006g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0006g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0006g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0006g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0008g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0009g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0009g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0009g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0010g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0010g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0010g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0010g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0011g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0011g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0011g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0011g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0012g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0012g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0013g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0013g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0013g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0014g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0014g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0014g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0015g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0016g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0016g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0016g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0017g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0017g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0017g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0018g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0018g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0019g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0019g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0020g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0020g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0021g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0021g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0022g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0022g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0023g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0023g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0024g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0024g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0025g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0025g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0026g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0026g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0027g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0028g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0028g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0029g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0030g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0033g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0036g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0038g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0039g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0042g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0043g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0046g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0047g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0048g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0001t0049g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0002t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0002t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0002t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0002t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0002t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0002t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0002t0007g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0002t0007g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0002t0007g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0002t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0002t0008g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0002t0012g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0002t0034g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0002t0041g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0002t0044g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0005t0015g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0005t0015g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0001c0007t0032g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0002c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0002c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0002c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0002c0003t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0002c0003t0008g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0002c0003t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0002c0003t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0002c0003t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0002c0003t0027g0248 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0002c0003t0031g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0002c0003t0040g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0002c0003t0045g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0002c0008t0037g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0003c0004t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0003c0004t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0003c0004t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0003c0004t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0003c0004t0002g0235 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0003c0004t0009g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0003c0004t0009g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0004c0009t0035g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| a0005c0006t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0004 | t0002 | g0211 | EUR | GBR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0129 | EUR | GBR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00140 | hp1 | a0003 | c0004 | t0001 | g0226 | EUR | GBR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | FIN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | FIN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00408 | hp2 | a0002 | c0003 | t0001 | g0042 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00438 | hp2 | a0001 | c0001 | t0028 | g0279 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00558 | hp2 | a0001 | c0001 | t0017 | g0044 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00597 | hp1 | a0001 | c0001 | t0019 | g0241 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00621 | hp1 | a0001 | c0001 | t0028 | g0130 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00733 | hp2 | a0001 | c0001 | t0012 | g0203 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00741 | hp1 | a0002 | c0003 | t0031 | g0109 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG00741 | hp2 | a0001 | c0001 | t0011 | g0218 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01070 | hp2 | a0001 | c0001 | t0023 | g0006 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01071 | hp1 | a0001 | c0001 | t0023 | g0005 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01074 | hp1 | a0001 | c0001 | t0047 | g0124 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01106 | hp1 | a0001 | c0001 | t0010 | g0286 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0022 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01167 | hp1 | a0002 | c0003 | t0040 | g0310 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01168 | hp1 | a0003 | c0004 | t0002 | g0058 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01169 | hp1 | a0002 | c0003 | t0045 | g0311 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01175 | hp1 | a0001 | c0001 | t0011 | g0242 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01192 | hp1 | a0001 | c0001 | t0009 | g0246 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01243 | hp2 | a0002 | c0003 | t0008 | g0013 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01257 | hp1 | a0001 | c0001 | t0038 | g0154 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0291 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01361 | hp1 | a0001 | c0001 | t0011 | g0208 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01361 | hp2 | a0003 | c0004 | t0001 | g0227 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01515 | hp2 | a0003 | c0004 | t0009 | g0301 | EUR | IBS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0313 | EUR | IBS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | IBS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01517 | hp2 | a0003 | c0004 | t0009 | g0292 | EUR | IBS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01884 | hp1 | a0001 | c0001 | t0013 | g0309 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0302 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0288 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01891 | hp2 | a0001 | c0001 | t0012 | g0289 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0253 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0076 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0187 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0256 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0075 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0137 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0053 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02080 | hp2 | a0001 | c0001 | t0006 | g0025 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02083 | hp1 | a0001 | c0001 | t0006 | g0060 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0153 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02135 | hp1 | a0001 | c0001 | t0017 | g0263 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02145 | hp1 | a0001 | c0002 | t0007 | g0190 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02155 | hp1 | a0001 | c0001 | t0029 | g0059 | EAS | CDX | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0192 | EAS | CDX | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | CDX | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CDX | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02257 | hp1 | a0001 | c0001 | t0010 | g0177 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02257 | hp2 | a0002 | c0003 | t0001 | g0141 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0306 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02280 | hp1 | a0001 | c0001 | t0042 | g0133 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0029 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0178 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02451 | hp1 | a0001 | c0002 | t0007 | g0308 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02451 | hp2 | a0002 | c0003 | t0001 | g0028 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02572 | hp2 | a0001 | c0001 | t0020 | g0131 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02602 | hp1 | a0001 | c0001 | t0010 | g0050 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02615 | hp1 | a0002 | c0003 | t0007 | g0009 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0271 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02622 | hp1 | a0001 | c0001 | t0021 | g0278 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0119 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02647 | hp2 | a0001 | c0002 | t0012 | g0049 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0017 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0063 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02717 | hp2 | a0001 | c0002 | t0034 | g0010 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02723 | hp2 | a0001 | c0001 | t0022 | g0004 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02735 | hp1 | a0001 | c0001 | t0011 | g0152 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02809 | hp1 | a0001 | c0002 | t0007 | g0007 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02809 | hp2 | a0001 | c0005 | t0015 | g0045 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02886 | hp1 | a0001 | c0002 | t0007 | g0052 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02896 | hp1 | a0001 | c0001 | t0013 | g0307 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0145 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02897 | hp1 | a0001 | c0001 | t0013 | g0303 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02922 | hp2 | a0004 | c0009 | t0035 | g0282 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02970 | hp1 | a0001 | c0001 | t0021 | g0021 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02970 | hp2 | a0001 | c0002 | t0005 | g0034 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02976 | hp1 | a0002 | c0003 | t0008 | g0065 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02976 | hp2 | a0001 | c0001 | t0046 | g0123 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03017 | hp1 | a0001 | c0001 | t0014 | g0096 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03041 | hp1 | a0001 | c0001 | t0010 | g0193 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0284 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03130 | hp2 | a0001 | c0002 | t0008 | g0008 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03139 | hp1 | a0001 | c0005 | t0015 | g0051 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03195 | hp2 | a0001 | c0001 | t0048 | g0121 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03209 | hp1 | a0001 | c0001 | t0036 | g0002 | AFR | MSL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03225 | hp2 | a0001 | c0001 | t0025 | g0027 | AFR | MSL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03239 | hp1 | a0001 | c0001 | t0016 | g0277 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03453 | hp2 | a0001 | c0002 | t0041 | g0140 | AFR | MSL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | MSL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03486 | hp2 | a0002 | c0008 | t0037 | g0098 | AFR | MSL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03491 | hp1 | a0001 | c0001 | t0014 | g0207 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03516 | hp2 | a0001 | c0001 | t0019 | g0188 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0064 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | STU | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03710 | hp1 | a0001 | c0007 | t0032 | g0101 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0274 | SAS | BEB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03831 | hp2 | a0001 | c0001 | t0014 | g0258 | SAS | BEB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03834 | hp2 | a0001 | c0001 | t0016 | g0233 | SAS | BEB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | BEB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0201 | SAS | BEB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | STU | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | STU | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0094 | SAS | STU | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18522 | hp2 | a0001 | c0001 | t0027 | g0026 | AFR | YRI | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | YRI | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18906 | hp2 | a0002 | c0003 | t0008 | g0066 | AFR | YRI | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18941 | hp1 | a0001 | c0001 | t0016 | g0293 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0320 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18950 | hp1 | a0001 | c0001 | t0026 | g0171 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18959 | hp1 | a0001 | c0001 | t0006 | g0080 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18960 | hp1 | a0001 | c0001 | t0006 | g0170 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18964 | hp2 | a0001 | c0001 | t0026 | g0210 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18967 | hp2 | a0001 | c0001 | t0009 | g0031 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18969 | hp2 | a0001 | c0001 | t0006 | g0077 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18973 | hp2 | a0001 | c0001 | t0039 | g0036 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18975 | hp1 | a0001 | c0001 | t0009 | g0136 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18988 | hp1 | a0005 | c0006 | t0001 | g0112 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18993 | hp2 | a0001 | c0001 | t0006 | g0165 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18994 | hp1 | a0001 | c0001 | t0018 | g0199 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19000 | hp1 | a0001 | c0001 | t0043 | g0255 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0166 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19030 | hp2 | a0001 | c0002 | t0007 | g0276 | AFR | LWK | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19043 | hp1 | a0001 | c0002 | t0005 | g0275 | AFR | LWK | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0318 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19060 | hp1 | a0001 | c0001 | t0006 | g0062 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19077 | hp1 | a0001 | c0001 | t0033 | g0268 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19080 | hp2 | a0001 | c0001 | t0024 | g0088 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19081 | hp1 | a0001 | c0001 | t0015 | g0168 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19083 | hp1 | a0001 | c0001 | t0006 | g0254 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19085 | hp2 | a0001 | c0001 | t0017 | g0269 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19089 | hp1 | a0001 | c0001 | t0030 | g0091 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0305 | AFR | YRI | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA19240 | hp2 | a0001 | c0001 | t0049 | g0122 | AFR | YRI | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | ASW | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA20129 | hp2 | a0001 | c0001 | t0022 | g0191 | AFR | ASW | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0314 | EUR | TSI | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA20905 | hp2 | a0001 | c0001 | t0024 | g0184 | SAS | GIH | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02109 | hp1 | a0001 | c0002 | t0005 | g0128 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02109 | hp2 | a0001 | c0001 | t0020 | g0138 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02486 | hp1 | a0001 | c0002 | t0008 | g0321 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG06807 | hp1 | a0002 | c0003 | t0008 | g0125 | AFR | USA | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| HG06807 | hp2 | a0001 | c0002 | t0044 | g0035 | AFR | USA | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA18955 | hp2 | a0001 | c0001 | t0018 | g0200 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA20300 | hp1 | a0001 | c0002 | t0005 | g0285 | AFR | USA | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA20300 | hp2 | a0001 | c0001 | t0025 | g0317 | AFR | USA | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0283 | AFR | LWK | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | LWK | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0004 | t0002 | g0235 | REF | REF | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| homoSapiens_grch38 | hp1 | a0002 | c0003 | t0027 | g0248 | REF | REF | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
| 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:2782116
|
G | A | 1 | a0003 | 7 | HG00099.hp1 HG00140.hp1 HG01168.hp1 others(4): Show |
missense_variant | MODERATE | c.178G>A | p.Asp60Asn | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/11 | 413/2943 | 178/588 | 60/195 | chrX | 2782116 | ||
| chrX:2789667
|
C | T | 1 | a0004 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.214C>T | p.Arg72Cys | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/11 | 449/2943 | 214/588 | 72/195 | chrX | 2789667 | ||
| chrX:2794571
|
A | AC | 1 | a0005 | 1 | NA18988.hp1 | frameshift_variant | HIGH | c.293dupC | p.Pro99fs | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/11 | 529/2943 | 294/588 | 98/195 | INFO_REALIGN_3_PRIME | chrX | 2794571 | |
| chrX:2806719
|
T | C | 4 | a0001a0003a0004others(1): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
missense_variant | MODERATE | c.392T>C | p.Leu131Pro | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/11 | 627/2943 | 392/588 | 131/195 | chrX | 2806719 |
| 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:2789693
|
C | T | 2 | a0001c0002a0002c0008 | 17 | HG02109.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
synonymous_variant | LOW | c.240C>T | p.Ser80Ser | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/11 | 475/2943 | 240/588 | 80/195 | chrX | 2789693 | ||
| chrX:2808207
|
T | C | 1 | a0001c0005 | 2 | HG02809.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.441T>C | p.Tyr147Tyr | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/11 | 676/2943 | 441/588 | 147/195 | chrX | 2808207 | ||
| chrX:2811367
|
C | A | 1 | a0001c0007 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.486C>A | p.Ile162Ile | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/11 | 721/2943 | 486/588 | 162/195 | chrX | 2811367 |
| 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:2752044
|
G | A | 1 | a0001c0001t0018 | 2 | NA18955.hp2 NA18994.hp1 |
5_prime_UTR_variant | MODIFIER | c.-231G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/11 | 231 | chrX | 2752044 | |||||
| chrX:2752093
|
G | A | 1 | a0001c0001t0029 | 1 | HG02155.hp1 | 5_prime_UTR_variant | MODIFIER | c.-182G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/11 | 182 | chrX | 2752093 | |||||
| chrX:2752241
|
A | G | 4 | a0001c0001t0046a0001c0001t0047a0001c0001t0048others(1): Show | 4 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-34A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/11 | 34 | chrX | 2752241 | |||||
| chrX:2814392
|
TC | T | 1 | a0002c0003t0045 | 1 | HG01169.hp1 | 3_prime_UTR_variant | MODIFIER | c.*16delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 16 | INFO_REALIGN_3_PRIME | chrX | 2814392 | ||||
| chrX:2814593
|
G | A | 10 | a0001c0001t0003a0001c0001t0005a0001c0001t0019others(7): Show | 64 | HG00408.hp1 HG00597.hp1 HG00673.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*213G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 213 | chrX | 2814593 | |||||
| chrX:2814693
|
T | C | 3 | a0001c0001t0012a0001c0001t0048a0001c0002t0012 | 4 | HG00733.hp2 HG01891.hp2 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*313T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 313 | chrX | 2814693 | |||||
| chrX:2815034
|
TG | T | 1 | a0001c0001t0030 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*659delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 659 | INFO_REALIGN_3_PRIME | chrX | 2815034 | ||||
| chrX:2815068
|
T | G | 40 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(37): Show | 232 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*688T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 688 | chrX | 2815068 | |||||
| chrX:2815169
|
G | A | 40 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(37): Show | 232 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*789G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 789 | chrX | 2815169 | |||||
| chrX:2815235
|
G | A | 50 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(47): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
3_prime_UTR_variant | MODIFIER | c.*855G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 855 | chrX | 2815235 | |||||
| chrX:2815251
|
C | G | 1 | a0001c0002t0041 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*871C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 871 | chrX | 2815251 | |||||
| chrX:2815298
|
TG | T | 1 | a0001c0001t0030 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*922delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 922 | INFO_REALIGN_3_PRIME | chrX | 2815298 | ||||
| chrX:2815313
|
G | T | 2 | a0002c0003t0040a0002c0003t0045 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*933G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 933 | chrX | 2815313 | |||||
| chrX:2815316
|
TG | T | 1 | a0002c0003t0045 | 1 | HG01169.hp1 | 3_prime_UTR_variant | MODIFIER | c.*938delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 938 | INFO_REALIGN_3_PRIME | chrX | 2815316 | ||||
| chrX:2815429
|
A | G | 1 | a0001c0001t0025 | 2 | HG03225.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1049A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1049 | chrX | 2815429 | |||||
| chrX:2815440
|
G | C | 1 | a0001c0001t0020 | 2 | HG02109.hp2 HG02572.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1060G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1060 | chrX | 2815440 | |||||
| chrX:2815600
|
A | G | 35 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(32): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*1220A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1220 | chrX | 2815600 | |||||
| chrX:2815627
|
G | A | 43 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(40): Show | 241 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(238): Show |
3_prime_UTR_variant | MODIFIER | c.*1247G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1247 | chrX | 2815627 | |||||
| chrX:2815695
|
G | GT | 1 | a0001c0001t0043 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1322dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1323 | INFO_REALIGN_3_PRIME | chrX | 2815695 | ||||
| chrX:2815743
|
A | G | 1 | a0001c0001t0039 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1363A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1363 | chrX | 2815743 | |||||
| chrX:2815761
|
G | A | 1 | a0002c0003t0031 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1381G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1381 | chrX | 2815761 | |||||
| chrX:2815800
|
T | TAC | 4 | a0001c0001t0012a0001c0001t0048a0001c0002t0012others(1): Show | 5 | HG00733.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1441_*1442dupAC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815800 | ||||
| chrX:2815800
|
T | TACAC | 1 | a0001c0001t0011 | 4 | HG00741.hp2 HG01175.hp1 HG01361.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1439_*1442dupACAC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815800 | ||||
| chrX:2815800
|
T | TACACAC | 2 | a0001c0001t0017a0001c0001t0018 | 5 | HG00558.hp2 HG02135.hp1 NA18955.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1437_*1442dupACAC others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815800 | ||||
| chrX:2815800
|
T | TACACACA others(1): Show |
1 | a0001c0007t0032 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1435_*1442dupACAC others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815800 | ||||
| chrX:2815800
|
T | TACACACA others(3): Show |
11 | a0001c0001t0005a0001c0001t0006a0001c0001t0020others(8): Show | 40 | HG00438.hp2 HG00621.hp1 HG01074.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1433_*1442dupACAC others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815800 | ||||
| chrX:2815800
|
T | TACACACA others(5): Show |
5 | a0001c0001t0003a0001c0001t0014a0001c0001t0016others(2): Show | 47 | HG00408.hp1 HG00673.hp1 HG01975.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1431_*1442dupACAC others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815800 | ||||
| chrX:2815800
|
T | TACACACA others(7): Show |
5 | a0001c0001t0002a0001c0001t0013a0001c0001t0019others(2): Show | 46 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1429_*1442dupACAC others(10): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815800 | ||||
| chrX:2815800
|
T | TACACACA others(9): Show |
2 | a0001c0001t0026a0004c0009t0035 | 3 | HG02922.hp2 NA18950.hp1 NA18964.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1427_*1442dupACAC others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815800 | ||||
| chrX:2815800
|
T | TACACACA others(13): Show |
1 | a0002c0003t0031 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1423_*1442dupACAC others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815800 | ||||
| chrX:2815800
|
T | TACACACA others(15): Show |
1 | a0001c0001t0042 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1421_*1442dupACAC others(18): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815800 | ||||
| chrX:2815800
|
T | TACATACA others(5): Show |
1 | a0001c0001t0010 | 4 | HG01106.hp1 HG02257.hp1 HG02602.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1423_*1424insTACA others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1424 | INFO_REALIGN_3_PRIME | chrX | 2815800 | ||||
| chrX:2815800
|
T | TACATACA others(7): Show |
2 | a0001c0001t0015a0001c0005t0015 | 3 | HG02809.hp2 HG03139.hp1 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1423_*1424insTACA others(10): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1424 | INFO_REALIGN_3_PRIME | chrX | 2815800 | ||||
| chrX:2815800
|
T | TACATACA others(9): Show |
12 | a0001c0001t0001a0001c0001t0004a0001c0001t0029others(9): Show | 133 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*1423_*1424insTACA others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1424 | INFO_REALIGN_3_PRIME | chrX | 2815800 | ||||
| chrX:2815800
|
T | TACATACA others(11): Show |
2 | a0001c0001t0009a0003c0004t0009 | 5 | HG01192.hp1 HG01515.hp2 HG01517.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1423_*1424insTACA others(14): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1424 | INFO_REALIGN_3_PRIME | chrX | 2815800 | ||||
| chrX:2815800
|
T | TACATACA others(13): Show |
1 | a0001c0001t0023 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1423_*1424insTACA others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1424 | INFO_REALIGN_3_PRIME | chrX | 2815800 | ||||
| chrX:2815800
|
T | TATATACA others(9): Show |
1 | a0001c0001t0024 | 2 | NA19080.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1421_*1422insTATA others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1422 | INFO_REALIGN_3_PRIME | chrX | 2815800 | ||||
| chrX:2815800
|
T | TATATACA others(11): Show |
1 | a0001c0001t0038 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1421_*1422insTATA others(14): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1422 | INFO_REALIGN_3_PRIME | chrX | 2815800 | ||||
| chrX:2815800
|
TAC | T | 4 | a0001c0001t0007a0001c0001t0022a0001c0002t0007others(1): Show | 9 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1441_*1442delAC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1441 | INFO_REALIGN_3_PRIME | chrX | 2815800 | ||||
| chrX:2815804
|
C | T | 1 | a0002c0008t0037 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1424C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1424 | chrX | 2815804 | |||||
| chrX:2815821
|
A | ACACACAC others(13): Show |
1 | a0002c0008t0037 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1442_*1443insACAC others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815821 | ||||
| chrX:2815821
|
A | C | 20 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(17): Show | 150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*1441A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1441 | chrX | 2815821 | |||||
| chrX:2815835
|
A | C | 1 | a0001c0001t0004 | 22 | HG00597.hp2 HG02071.hp1 HG02129.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1455A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1455 | chrX | 2815835 | |||||
| chrX:2815968
|
A | C | 1 | a0001c0001t0013 | 3 | HG01884.hp1 HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1588A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1588 | chrX | 2815968 | |||||
| chrX:2816014
|
C | T | 1 | a0001c0001t0021 | 2 | HG02622.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1634C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1634 | chrX | 2816014 | |||||
| chrX:2816107
|
TA | T | 1 | a0001c0001t0030 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1730delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1730 | INFO_REALIGN_3_PRIME | chrX | 2816107 | ||||
| chrX:2816415
|
AC | A | 1 | a0001c0001t0030 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2038delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 2038 | INFO_REALIGN_3_PRIME | chrX | 2816415 |
| 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:2752405
|
C | G | 1 | a0001c0002t0008g0321 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.61+70C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2752405 | ||||||
| chrX:2752450
|
A | G | 3 | a0001c0001t0003g0319a0001c0001t0004g0318a0001c0001t0004g0320 | 3 | NA18943.hp2 NA18968.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.61+115A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2752450 | ||||||
| chrX:2752500
|
G | A | 120 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(117): Show | 120 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.61+165G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2752500 | ||||||
| chrX:2752551
|
G | T | 145 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(142): Show | 145 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.61+216G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2752551 | ||||||
| chrX:2752558
|
G | A | 5 | a0001c0001t0046g0123a0001c0001t0047g0124a0001c0001t0048g0121others(2): Show | 5 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+223G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2752558 | ||||||
| chrX:2752584
|
A | G | 1 | a0001c0001t0025g0317 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.61+249A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2752584 | ||||||
| chrX:2752592
|
GT | G | 1 | a0001c0001t0004g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.61+261delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2752592 | |||||
| chrX:2752631
|
A | G | 4 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0002g0313others(1): Show | 4 | HG00642.hp1 HG01516.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+296A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2752631 | ||||||
| chrX:2752750
|
TC | T | 1 | a0001c0001t0003g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.61+418delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2752750 | |||||
| chrX:2753131
|
G | GT | 1 | a0001c0001t0004g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.61+799dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2753131 | |||||
| chrX:2753244
|
G | T | 121 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(118): Show | 121 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.61+909G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753244 | ||||||
| chrX:2753325
|
A | G | 26 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0264others(23): Show | 26 | HG01496.hp1 HG01981.hp2 HG01993.hp2 others(23): Show |
intron_variant | MODIFIER | c.61+990A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753325 | ||||||
| chrX:2753464
|
C | CA | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.61+1131dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2753464 | |||||
| chrX:2753509
|
A | G | 33 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0264others(30): Show | 33 | HG01074.hp1 HG01496.hp1 HG01981.hp2 others(30): Show |
intron_variant | MODIFIER | c.61+1174A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753509 | ||||||
| chrX:2753519
|
G | A | 1 | a0002c0003t0008g0013 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.61+1184G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753519 | ||||||
| chrX:2753583
|
C | CT | 3 | a0001c0001t0003g0319a0001c0001t0004g0320a0001c0001t0006g0254 | 3 | NA18943.hp2 NA18968.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.61+1260dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2753583 | |||||
| chrX:2753583
|
CT | C | 1 | a0001c0001t0001g0014 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.61+1260delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2753583 | |||||
| chrX:2753594
|
T | C | 5 | a0001c0001t0046g0123a0001c0001t0047g0124a0001c0001t0048g0121others(2): Show | 5 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+1259T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753594 | ||||||
| chrX:2753627
|
G | C | 13 | a0001c0001t0001g0287a0001c0001t0001g0315a0001c0001t0001g0316others(10): Show | 13 | HG00642.hp1 HG01106.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+1292G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753627 | ||||||
| chrX:2753661
|
C | CA | 1 | a0001c0001t0004g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.61+1328dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2753661 | |||||
| chrX:2753727
|
T | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0135others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.61+1392T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753727 | ||||||
| chrX:2753762
|
T | G | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.61+1427T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753762 | ||||||
| chrX:2753827
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.61+1492C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753827 | ||||||
| chrX:2753867
|
T | TG | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.61+1533dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2753867 | |||||
| chrX:2753871
|
C | T | 1 | a0001c0001t0003g0253 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.61+1536C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753871 | ||||||
| chrX:2753912
|
G | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0135others(124): Show | 128 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.61+1577G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753912 | ||||||
| chrX:2753940
|
AC | A | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.61+1607delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2753940 | |||||
| chrX:2754044
|
T | TG | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.61+1711dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2754044 | |||||
| chrX:2754054
|
G | GT | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.61+1721dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2754054 | |||||
| chrX:2754064
|
A | T | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.61+1729A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754064 | ||||||
| chrX:2754065
|
T | G | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.61+1730T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754065 | ||||||
| chrX:2754066
|
G | T | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.61+1731G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754066 | ||||||
| chrX:2754118
|
A | AG | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.61+1786dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2754118 | |||||
| chrX:2754153
|
C | CG | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.61+1820dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2754153 | |||||
| chrX:2754153
|
C | T | 1 | a0001c0001t0005g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.61+1818C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754153 | ||||||
| chrX:2754174
|
C | G | 40 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(37): Show | 40 | HG00642.hp1 HG00738.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.61+1839C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754174 | ||||||
| chrX:2754464
|
A | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0118a0001c0001t0001g0134others(89): Show | 93 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.61+2129A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754464 | ||||||
| chrX:2754506
|
A | C | 5 | a0001c0001t0046g0123a0001c0001t0047g0124a0001c0001t0048g0121others(2): Show | 5 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+2171A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754506 | ||||||
| chrX:2754572
|
T | G | 1 | a0001c0001t0002g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.61+2237T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754572 | ||||||
| chrX:2754574
|
G | T | 1 | a0001c0001t0002g0117 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.61+2239G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754574 | ||||||
| chrX:2754651
|
G | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0118a0001c0001t0001g0134others(126): Show | 130 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.61+2316G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754651 | ||||||
| chrX:2754694
|
T | C | 5 | a0001c0001t0046g0123a0001c0001t0047g0124a0001c0001t0048g0121others(2): Show | 5 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+2359T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754694 | ||||||
| chrX:2754833
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.61+2498G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754833 | ||||||
| chrX:2755057
|
C | T | 27 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(24): Show | 27 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.61+2722C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755057 | ||||||
| chrX:2755123
|
G | GT | 1 | a0001c0001t0004g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.61+2788_61+2789ins others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755123 | ||||||
| chrX:2755161
|
C | T | 5 | a0001c0001t0046g0123a0001c0001t0047g0124a0001c0001t0048g0121others(2): Show | 5 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+2826C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755161 | ||||||
| chrX:2755162
|
G | A | 3 | a0001c0001t0001g0315a0001c0001t0002g0313a0001c0001t0002g0314 | 3 | HG01516.hp2 HG03540.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.61+2827G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755162 | ||||||
| chrX:2755338
|
T | A | 1 | a0001c0001t0003g0319 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.61+3003T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755338 | ||||||
| chrX:2755419
|
C | T | 1 | a0001c0001t0021g0278 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.61+3084C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755419 | ||||||
| chrX:2755449
|
T | TG | 18 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0264others(15): Show | 18 | HG01496.hp1 HG01981.hp2 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.61+3116dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2755449 | |||||
| chrX:2755522
|
G | A | 21 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0264others(18): Show | 21 | HG01496.hp1 HG01981.hp2 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.61+3187G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755522 | ||||||
| chrX:2755526
|
T | C | 4 | a0001c0001t0046g0123a0001c0001t0047g0124a0001c0001t0048g0121others(1): Show | 4 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+3191T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755526 | ||||||
| chrX:2755594
|
C | A | 1 | a0001c0001t0012g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.61+3259C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755594 | ||||||
| chrX:2755696
|
G | A | 1 | a0001c0001t0028g0130 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.61+3361G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755696 | ||||||
| chrX:2755881
|
T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0118others(162): Show | 166 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.61+3546T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755881 | ||||||
| chrX:2756098
|
G | A | 4 | a0001c0001t0046g0123a0001c0001t0047g0124a0001c0001t0048g0121others(1): Show | 4 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+3763G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756098 | ||||||
| chrX:2756235
|
C | T | 37 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(34): Show | 37 | HG00642.hp1 HG00738.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.61+3900C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756235 | ||||||
| chrX:2756249
|
A | G | 1 | a0001c0002t0005g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.61+3914A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756249 | ||||||
| chrX:2756328
|
AG | A | 3 | a0001c0001t0022g0004a0001c0001t0023g0005a0001c0001t0023g0006 | 3 | HG01070.hp2 HG01071.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.61+3997delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2756328 | |||||
| chrX:2756364
|
G | T | 3 | a0001c0001t0022g0004a0001c0001t0023g0005a0001c0001t0023g0006 | 3 | HG01070.hp2 HG01071.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.61+4029G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756364 | ||||||
| chrX:2756373
|
A | T | 1 | a0001c0001t0005g0288 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.61+4038A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756373 | ||||||
| chrX:2756593
|
ATAAAT | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0118a0001c0001t0001g0134others(83): Show | 87 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.61+4263_61+4267del others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2756593 | |||||
| chrX:2756701
|
C | T | 1 | a0001c0001t0004g0318 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.61+4366C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756701 | ||||||
| chrX:2756706
|
G | A | 1 | a0001c0001t0006g0017 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.61+4371G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756706 | ||||||
| chrX:2756706
|
G | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(166): Show | 170 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.61+4371G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756706 | ||||||
| chrX:2756709
|
C | G | 4 | a0001c0001t0046g0123a0001c0001t0047g0124a0001c0001t0048g0121others(1): Show | 4 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+4374C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756709 | ||||||
| chrX:2756801
|
G | A | 4 | a0001c0001t0046g0123a0001c0001t0047g0124a0001c0001t0048g0121others(1): Show | 4 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+4466G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756801 | ||||||
| chrX:2756910
|
G | A | 1 | a0004c0009t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.61+4575G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756910 | ||||||
| chrX:2757065
|
C | T | 1 | a0001c0001t0004g0116 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.61+4730C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2757065 | ||||||
| chrX:2757135
|
C | CG | 1 | a0001c0001t0004g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.61+4802dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757135 | |||||
| chrX:2757421
|
G | C | 193 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(190): Show | 193 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.61+5086G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2757421 | ||||||
| chrX:2757449
|
G | A | 3 | a0001c0001t0022g0004a0001c0001t0023g0005a0001c0001t0023g0006 | 3 | HG01070.hp2 HG01071.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.61+5114G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2757449 | ||||||
| chrX:2757475
|
G | C | 1 | a0001c0001t0002g0117 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.61+5140G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2757475 | ||||||
| chrX:2757566
|
CTGAGTAC others(7): Show |
C | 1 | a0001c0001t0001g0023 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.61+5238_61+5251del others(14): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757566 | |||||
| chrX:2757654
|
GT | G | 1 | a0001c0001t0020g0131 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.61+5322delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757654 | |||||
| chrX:2757740
|
G | A | 2 | a0001c0001t0003g0024a0001c0001t0003g0120 | 2 | NA18971.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.61+5405G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2757740 | ||||||
| chrX:2757797
|
C | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0114a0001c0001t0001g0115others(3): Show | 6 | HG02523.hp2 NA18981.hp1 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+5462C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2757797 | ||||||
| chrX:2757971
|
C | CA | 19 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0139others(16): Show | 19 | HG00741.hp2 HG01257.hp2 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.61+5661dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757971 | |||||
| chrX:2757971
|
C | CAA | 2 | a0001c0001t0002g0132a0001c0001t0042g0133 | 2 | HG02280.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.61+5660_61+5661dup others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757971 | |||||
| chrX:2757971
|
CA | C | 37 | a0001c0001t0001g0251a0001c0001t0001g0260a0001c0001t0001g0261others(34): Show | 37 | HG01074.hp1 HG01109.hp2 HG01993.hp2 others(34): Show |
intron_variant | MODIFIER | c.61+5661delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757971 | |||||
| chrX:2757971
|
CAA | C | 1 | a0001c0001t0001g0270 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.61+5660_61+5661del others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757971 | |||||
| chrX:2757971
|
CAAAAA | C | 2 | a0001c0001t0025g0317a0001c0002t0008g0321 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.61+5657_61+5661del others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757971 | |||||
| chrX:2757971
|
CAAAAAA | C | 13 | a0001c0001t0001g0196a0001c0001t0001g0204a0001c0001t0001g0205others(10): Show | 13 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.61+5656_61+5661del others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757971 | |||||
| chrX:2757971
|
CAAAAAAA | C | 104 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(101): Show | 104 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.61+5655_61+5661del others(7): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757971 | |||||
| chrX:2757971
|
CAAAAAAA others(1): Show |
C | 1 | a0001c0002t0005g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.61+5654_61+5661del others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757971 | |||||
| chrX:2757971
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.61+5650_61+5661del others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757971 | |||||
| chrX:2757971
|
CAAAAAAA others(6): Show |
C | 29 | a0001c0001t0001g0209a0001c0001t0001g0214a0001c0001t0001g0304others(26): Show | 29 | HG00099.hp2 HG00642.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.61+5649_61+5661del others(13): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757971 | |||||
| chrX:2758018
|
C | T | 8 | a0001c0001t0003g0283a0001c0001t0005g0003a0001c0001t0005g0284others(5): Show | 8 | HG01106.hp1 HG01261.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+5683C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758018 | ||||||
| chrX:2758042
|
C | T | 13 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0267others(10): Show | 13 | HG02004.hp2 HG02135.hp1 HG03669.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+5707C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758042 | ||||||
| chrX:2758044
|
C | G | 13 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0267others(10): Show | 13 | HG02004.hp2 HG02135.hp1 HG03669.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+5709C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758044 | ||||||
| chrX:2758119
|
T | C | 191 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.61+5784T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758119 | ||||||
| chrX:2758123
|
G | GC | 1 | a0001c0001t0009g0031 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.61+5793dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2758123 | |||||
| chrX:2758175
|
AG | A | 1 | a0001c0001t0001g0249 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.61+5842delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2758175 | |||||
| chrX:2758380
|
AT | A | 1 | a0001c0001t0001g0032 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.61+6049delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2758380 | |||||
| chrX:2758395
|
C | G | 2 | a0001c0001t0002g0247a0001c0001t0038g0154 | 2 | HG01257.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.61+6060C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758395 | ||||||
| chrX:2758408
|
A | G | 1 | a0001c0001t0005g0145 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.61+6073A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758408 | ||||||
| chrX:2758411
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.61+6076C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758411 | ||||||
| chrX:2758446
|
C | T | 1 | a0001c0001t0004g0192 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.61+6111C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758446 | ||||||
| chrX:2758457
|
G | A | 3 | a0001c0001t0002g0108a0001c0001t0003g0319a0001c0001t0004g0192 | 3 | HG02155.hp2 HG04115.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.61+6122G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758457 | ||||||
| chrX:2758472
|
C | G | 1 | a0001c0001t0004g0192 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.61+6137C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758472 | ||||||
| chrX:2758639
|
G | A | 7 | a0001c0001t0005g0020a0001c0001t0005g0022a0001c0001t0021g0021others(4): Show | 7 | HG01109.hp2 HG02630.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+6304G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758639 | ||||||
| chrX:2758814
|
G | C | 1 | a0001c0001t0046g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.61+6479G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758814 | ||||||
| chrX:2758874
|
C | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.61+6539C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758874 | ||||||
| chrX:2758881
|
C | A | 1 | a0001c0001t0002g0257 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.61+6546C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758881 | ||||||
| chrX:2758944
|
T | C | 10 | a0001c0001t0001g0134a0001c0001t0003g0047a0001c0001t0003g0048others(7): Show | 10 | HG02559.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.61+6609T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758944 | ||||||
| chrX:2758952
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0107a0001c0001t0001g0209 | 3 | HG01168.hp2 HG01169.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.61+6617C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758952 | ||||||
| chrX:2758956
|
T | C | 5 | a0001c0001t0001g0032a0001c0001t0001g0107a0001c0001t0001g0143others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+6621T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758956 | ||||||
| chrX:2758956
|
T | TTATC | 234 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.61+6627_61+6630dup others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2758956 | |||||
| chrX:2759032
|
GTATC | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.61+6706_61+6709del others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2759032 | |||||
| chrX:2759050
|
G | A | 235 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.61+6715G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759050 | ||||||
| chrX:2759060
|
C | G | 4 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0004g0116others(1): Show | 4 | NA18963.hp1 NA18967.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+6725C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759060 | ||||||
| chrX:2759093
|
G | A | 235 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.61+6758G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759093 | ||||||
| chrX:2759094
|
T | C | 10 | a0001c0001t0001g0214a0001c0001t0001g0249a0001c0001t0010g0050others(7): Show | 10 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+6759T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759094 | ||||||
| chrX:2759112
|
C | T | 1 | a0001c0001t0010g0177 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61+6777C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759112 | ||||||
| chrX:2759113
|
A | T | 235 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.61+6778A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759113 | ||||||
| chrX:2759121
|
T | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.61+6786T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759121 | ||||||
| chrX:2759132
|
G | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(215): Show | 219 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.61+6797G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759132 | ||||||
| chrX:2759317
|
A | G | 37 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0213others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.61+6982A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759317 | ||||||
| chrX:2759369
|
C | T | 1 | a0001c0007t0032g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.61+7034C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759369 | ||||||
| chrX:2759370
|
G | A | 53 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0001g0142others(50): Show | 53 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.61+7035G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759370 | ||||||
| chrX:2759375
|
A | AGGAGGTA others(9): Show |
1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.61+7072_61+7087dup others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2759375 | |||||
| chrX:2759375
|
AGGAGGTA others(9): Show |
A | 1 | a0002c0003t0031g0109 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.61+7072_61+7087del others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2759375 | |||||
| chrX:2759443
|
G | A | 11 | a0001c0001t0001g0304a0001c0001t0005g0288a0001c0001t0005g0305others(8): Show | 11 | HG01891.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+7108G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759443 | ||||||
| chrX:2759506
|
C | T | 74 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0043others(71): Show | 74 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.61+7171C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759506 | ||||||
| chrX:2759548
|
G | A | 19 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0134others(16): Show | 19 | HG01243.hp2 HG02559.hp2 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.61+7213G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759548 | ||||||
| chrX:2759656
|
G | C | 7 | a0001c0001t0005g0020a0001c0001t0005g0022a0001c0001t0021g0021others(4): Show | 7 | HG01109.hp2 HG02630.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+7321G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759656 | ||||||
| chrX:2759704
|
A | G | 18 | a0001c0001t0001g0134a0001c0001t0003g0047a0001c0001t0003g0048others(15): Show | 18 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.61+7369A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759704 | ||||||
| chrX:2759723
|
G | GC | 1 | a0001c0001t0002g0156 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.61+7394dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2759723 | |||||
| chrX:2759809
|
C | T | 80 | a0001c0001t0001g0016a0001c0001t0001g0037a0001c0001t0001g0038others(77): Show | 80 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.61+7474C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759809 | ||||||
| chrX:2759815
|
C | T | 10 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0196others(7): Show | 10 | HG00423.hp2 NA18945.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+7480C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759815 | ||||||
| chrX:2759816
|
G | A | 6 | a0001c0001t0001g0118a0001c0001t0001g0159a0001c0001t0002g0161others(3): Show | 6 | HG00597.hp2 HG00621.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+7481G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759816 | ||||||
| chrX:2759819
|
A | T | 55 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0134others(52): Show | 55 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.61+7484A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759819 | ||||||
| chrX:2759856
|
G | A | 2 | a0001c0001t0002g0230a0001c0001t0004g0053 | 2 | HG02071.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.61+7521G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759856 | ||||||
| chrX:2759955
|
T | TCTGCATG others(4): Show |
139 | a0001c0001t0001g0016a0001c0001t0001g0037a0001c0001t0001g0038others(136): Show | 139 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.61+7621_61+7622ins others(11): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2759955 | |||||
| chrX:2760019
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0003g0039 | 2 | HG00673.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.61+7684C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760019 | ||||||
| chrX:2760034
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.61+7699C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760034 | ||||||
| chrX:2760082
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.61+7747C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760082 | ||||||
| chrX:2760124
|
G | A | 14 | a0001c0001t0001g0249a0001c0001t0002g0151a0001c0001t0005g0288others(11): Show | 14 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.61+7789G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760124 | ||||||
| chrX:2760181
|
GA | G | 8 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0005g0029others(5): Show | 8 | HG02257.hp2 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+7856delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2760181 | |||||
| chrX:2760192
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0002g0040 | 2 | HG02027.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.61+7857T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760192 | ||||||
| chrX:2760370
|
T | C | 1 | a0001c0001t0006g0254 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.61+8035T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760370 | ||||||
| chrX:2760523
|
CAGG | C | 5 | a0001c0001t0005g0020a0001c0001t0005g0022a0001c0001t0021g0021others(2): Show | 5 | HG01109.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+8191_61+8193del others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2760523 | |||||
| chrX:2760562
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.61+8227C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760562 | ||||||
| chrX:2760579
|
C | CA | 61 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0037others(58): Show | 61 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.61+8260dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2760579 | |||||
| chrX:2760579
|
C | CAA | 2 | a0001c0001t0006g0017a0001c0001t0017g0263 | 2 | HG02135.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.61+8259_61+8260dup others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2760579 | |||||
| chrX:2760579
|
CA | C | 39 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0134others(36): Show | 39 | HG00733.hp1 HG01109.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.61+8260delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2760579 | |||||
| chrX:2760581
|
A | C | 25 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0249others(22): Show | 25 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.61+8246A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760581 | ||||||
| chrX:2760582
|
A | C | 2 | a0001c0001t0002g0151a0001c0001t0011g0152 | 2 | HG01358.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.61+8247A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760582 | ||||||
| chrX:2760583
|
A | C | 25 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0249others(22): Show | 25 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.61+8248A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760583 | ||||||
| chrX:2760584
|
A | C | 2 | a0001c0001t0002g0151a0001c0001t0011g0152 | 2 | HG01358.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.61+8249A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760584 | ||||||
| chrX:2760585
|
A | C | 14 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0003g0137others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.61+8250A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760585 | ||||||
| chrX:2760734
|
C | CA | 5 | a0001c0001t0004g0167a0001c0001t0004g0320a0001c0001t0015g0168others(2): Show | 5 | HG00438.hp2 HG03239.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+8421dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2760734 | |||||
| chrX:2760734
|
CA | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(200): Show | 204 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.61+8421delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2760734 | |||||
| chrX:2760734
|
CAA | C | 31 | a0001c0001t0001g0057a0001c0001t0001g0134a0001c0001t0001g0142others(28): Show | 31 | HG00280.hp1 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.61+8420_61+8421del others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2760734 | |||||
| chrX:2760734
|
CAAA | C | 26 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0104others(23): Show | 26 | HG00323.hp1 HG00423.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.61+8419_61+8421del others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2760734 | |||||
| chrX:2760734
|
CAAAA | C | 1 | a0002c0003t0031g0109 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.61+8418_61+8421del others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2760734 | |||||
| chrX:2760777
|
A | AG | 1 | a0001c0001t0001g0229 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.61+8444dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2760777 | |||||
| chrX:2760816
|
C | A | 3 | a0001c0002t0001g0011a0001c0002t0034g0010a0002c0003t0001g0028 | 3 | HG02451.hp2 HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.61+8481C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760816 | ||||||
| chrX:2761052
|
T | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(183): Show | 187 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.61+8717T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2761052 | ||||||
| chrX:2761171
|
TA | T | 1 | a0001c0001t0001g0229 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.61+8839delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2761171 | |||||
| chrX:2761351
|
GC | G | 1 | a0001c0001t0001g0229 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.61+9019delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2761351 | |||||
| chrX:2761465
|
G | A | 11 | a0001c0001t0001g0142a0001c0001t0003g0137a0001c0001t0005g0029others(8): Show | 11 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.62-9085G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2761465 | ||||||
| chrX:2761469
|
T | C | 5 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0002g0108others(2): Show | 5 | HG04115.hp1 NA18946.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-9081T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2761469 | ||||||
| chrX:2761590
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.62-8960C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2761590 | ||||||
| chrX:2761758
|
G | A | 32 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0134others(29): Show | 32 | HG01109.hp2 HG01243.hp2 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.62-8792G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2761758 | ||||||
| chrX:2761846
|
T | G | 1 | a0001c0001t0001g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.62-8704T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2761846 | ||||||
| chrX:2761888
|
G | A | 5 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0002g0108others(2): Show | 5 | HG04115.hp1 NA18946.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-8662G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2761888 | ||||||
| chrX:2761895
|
A | G | 1 | a0001c0002t0044g0035 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.62-8655A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2761895 | ||||||
| chrX:2761901
|
TG | T | 1 | a0001c0001t0046g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.62-8646delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2761901 | |||||
| chrX:2761908
|
G | T | 54 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0104others(51): Show | 54 | HG00323.hp1 HG00423.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.62-8642G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2761908 | ||||||
| chrX:2762116
|
G | A | 54 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0104others(51): Show | 54 | HG00323.hp1 HG00423.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.62-8434G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762116 | ||||||
| chrX:2762144
|
C | T | 55 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0104others(52): Show | 55 | HG00323.hp1 HG00423.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.62-8406C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762144 | ||||||
| chrX:2762146
|
G | C | 5 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0002g0108others(2): Show | 5 | HG04115.hp1 NA18946.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-8404G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762146 | ||||||
| chrX:2762258
|
T | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(246): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.62-8292T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762258 | ||||||
| chrX:2762304
|
C | T | 1 | a0001c0002t0007g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.62-8246C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762304 | ||||||
| chrX:2762337
|
A | G | 1 | a0001c0002t0007g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.62-8213A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762337 | ||||||
| chrX:2762414
|
C | T | 3 | a0001c0001t0025g0027a0001c0001t0049g0122a0001c0002t0008g0321 | 3 | HG02486.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.62-8136C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762414 | ||||||
| chrX:2762428
|
G | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0107 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.62-8122G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762428 | ||||||
| chrX:2762597
|
CAATTAGA others(1): Show |
C | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7950_62-7943del others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2762597 | |||||
| chrX:2762631
|
T | TG | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7915dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2762631 | |||||
| chrX:2762642
|
T | TG | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7908_62-7907ins others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762642 | ||||||
| chrX:2762646
|
A | T | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7904A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762646 | ||||||
| chrX:2762648
|
T | G | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7902T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762648 | ||||||
| chrX:2762657
|
G | C | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7893G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762657 | ||||||
| chrX:2762666
|
GC | G | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7878delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2762666 | |||||
| chrX:2762730
|
A | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(258): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.62-7820A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762730 | ||||||
| chrX:2762731
|
C | T | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0002g0108others(1): Show | 4 | HG04115.hp1 NA18946.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-7819C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762731 | ||||||
| chrX:2762796
|
G | T | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7754G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762796 | ||||||
| chrX:2762797
|
T | G | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7753T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762797 | ||||||
| chrX:2762850
|
A | G | 1 | a0001c0001t0003g0176 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.62-7700A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762850 | ||||||
| chrX:2763159
|
G | GT | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7391_62-7390ins others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763159 | ||||||
| chrX:2763161
|
T | C | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7389T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763161 | ||||||
| chrX:2763164
|
A | AC | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7385dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2763164 | |||||
| chrX:2763165
|
C | CACCA | 40 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0043others(37): Show | 40 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.62-7384_62-7381dup others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2763165 | |||||
| chrX:2763174
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.62-7376G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763174 | ||||||
| chrX:2763174
|
G | GC | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7373dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2763174 | |||||
| chrX:2763182
|
T | TG | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7368_62-7367ins others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763182 | ||||||
| chrX:2763188
|
A | AT | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7357dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2763188 | |||||
| chrX:2763196
|
T | TC | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7354_62-7353ins others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763196 | ||||||
| chrX:2763203
|
A | AG | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7344dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2763203 | |||||
| chrX:2763290
|
G | A | 11 | a0001c0001t0001g0014a0001c0001t0001g0057a0001c0001t0001g0183others(8): Show | 11 | HG00280.hp1 HG01123.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.62-7260G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763290 | ||||||
| chrX:2763374
|
TA | T | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7170delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2763374 | |||||
| chrX:2763391
|
T | TC | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7159_62-7158ins others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763391 | ||||||
| chrX:2763414
|
G | GA | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7133dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2763414 | |||||
| chrX:2763461
|
TC | T | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7086delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2763461 | |||||
| chrX:2763470
|
C | A | 1 | a0001c0001t0026g0210 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.62-7080C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763470 | ||||||
| chrX:2763471
|
A | G | 272 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(269): Show | 272 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.62-7079A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763471 | ||||||
| chrX:2763474
|
TG | T | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7074delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2763474 | |||||
| chrX:2763484
|
A | AG | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7060dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2763484 | |||||
| chrX:2763484
|
AG | A | 1 | a0001c0001t0001g0032 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.62-7060delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2763484 | |||||
| chrX:2763495
|
A | AG | 1 | a0001c0001t0001g0213 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.62-7049dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2763495 | |||||
| chrX:2763510
|
C | G | 268 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(265): Show | 268 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.62-7040C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763510 | ||||||
| chrX:2763775
|
A | C | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.62-6775A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763775 | ||||||
| chrX:2763790
|
T | A | 23 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0135others(20): Show | 23 | HG00323.hp1 HG00423.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.62-6760T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763790 | ||||||
| chrX:2763829
|
A | G | 1 | a0001c0002t0005g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.62-6721A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763829 | ||||||
| chrX:2763831
|
G | C | 1 | a0001c0001t0001g0264 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.62-6719G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763831 | ||||||
| chrX:2763837
|
A | G | 25 | a0001c0001t0001g0015a0001c0001t0001g0037a0001c0001t0001g0038others(22): Show | 25 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.62-6713A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763837 | ||||||
| chrX:2763848
|
G | T | 1 | a0001c0007t0032g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.62-6702G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763848 | ||||||
| chrX:2763891
|
T | G | 232 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0018others(229): Show | 232 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.62-6659T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763891 | ||||||
| chrX:2763925
|
G | C | 59 | a0001c0001t0001g0015a0001c0001t0001g0037a0001c0001t0001g0038others(56): Show | 59 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.62-6625G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763925 | ||||||
| chrX:2763977
|
G | A | 261 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0018others(258): Show | 261 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.62-6573G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763977 | ||||||
| chrX:2764108
|
T | C | 313 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(310): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.62-6442T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764108 | ||||||
| chrX:2764120
|
C | T | 2 | a0001c0001t0003g0283a0001c0001t0046g0123 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.62-6430C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764120 | ||||||
| chrX:2764135
|
T | G | 314 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(311): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.62-6415T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764135 | ||||||
| chrX:2764172
|
C | T | 2 | a0001c0001t0001g0142a0001c0002t0044g0035 | 2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.62-6378C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764172 | ||||||
| chrX:2764175
|
C | T | 2 | a0001c0001t0001g0142a0001c0002t0044g0035 | 2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.62-6375C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764175 | ||||||
| chrX:2764227
|
G | A | 23 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0214others(20): Show | 23 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.62-6323G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764227 | ||||||
| chrX:2764349
|
C | A | 1 | a0002c0003t0008g0013 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.62-6201C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764349 | ||||||
| chrX:2764367
|
G | A | 1 | a0001c0001t0014g0258 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.62-6183G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764367 | ||||||
| chrX:2764369
|
C | G | 1 | a0001c0001t0014g0258 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.62-6181C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764369 | ||||||
| chrX:2764377
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.62-6173C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764377 | ||||||
| chrX:2764654
|
C | A | 1 | a0001c0001t0043g0255 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.62-5896C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764654 | ||||||
| chrX:2764700
|
T | C | 2 | a0001c0001t0001g0142a0001c0002t0044g0035 | 2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.62-5850T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764700 | ||||||
| chrX:2764722
|
GA | G | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-5825delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2764722 | |||||
| chrX:2764778
|
T | C | 28 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.62-5772T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764778 | ||||||
| chrX:2764814
|
G | T | 7 | a0001c0001t0003g0283a0001c0001t0005g0003a0001c0001t0005g0020others(4): Show | 7 | HG01261.hp1 HG02630.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-5736G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764814 | ||||||
| chrX:2764873
|
A | T | 43 | a0001c0001t0001g0015a0001c0001t0001g0037a0001c0001t0001g0038others(40): Show | 43 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.62-5677A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764873 | ||||||
| chrX:2764874
|
T | C | 43 | a0001c0001t0001g0015a0001c0001t0001g0037a0001c0001t0001g0038others(40): Show | 43 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.62-5676T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764874 | ||||||
| chrX:2764884
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.62-5666C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764884 | ||||||
| chrX:2764906
|
T | G | 3 | a0001c0001t0022g0004a0001c0001t0023g0005a0001c0001t0023g0006 | 3 | HG01070.hp2 HG01071.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.62-5644T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764906 | ||||||
| chrX:2764989
|
C | T | 19 | a0001c0001t0001g0093a0001c0001t0002g0108a0001c0001t0003g0283others(16): Show | 19 | HG01261.hp1 HG02451.hp2 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.62-5561C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764989 | ||||||
| chrX:2765011
|
A | C | 2 | a0001c0001t0004g0245a0001c0001t0006g0062 | 2 | NA19002.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.62-5539A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765011 | ||||||
| chrX:2765041
|
C | CA | 202 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(199): Show | 203 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.62-5485dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765041 | |||||
| chrX:2765041
|
C | CAA | 54 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0069others(51): Show | 54 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.62-5486_62-5485dup others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765041 | |||||
| chrX:2765041
|
C | CAAA | 11 | a0001c0001t0001g0093a0001c0001t0001g0172a0001c0001t0003g0047others(8): Show | 11 | HG02572.hp2 HG02809.hp2 HG03130.hp2 others(8): Show |
intron_variant | MODIFIER | c.62-5487_62-5485dup others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765041 | |||||
| chrX:2765041
|
C | CAAAA | 3 | a0001c0001t0005g0119a0001c0001t0013g0309a0001c0002t0005g0128 | 3 | HG01884.hp1 HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.62-5488_62-5485dup others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765041 | |||||
| chrX:2765041
|
CA | C | 4 | a0001c0001t0001g0142a0001c0002t0007g0052a0001c0002t0007g0190others(1): Show | 4 | HG02145.hp1 HG02886.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-5485delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765041 | |||||
| chrX:2765041
|
CAAAAA | C | 1 | a0001c0001t0030g0091 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.62-5489_62-5485del others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765041 | |||||
| chrX:2765041
|
CAAAAAA | C | 6 | a0001c0001t0003g0012a0001c0001t0003g0202a0001c0001t0005g0288others(3): Show | 6 | HG00558.hp2 HG01891.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-5490_62-5485del others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765041 | |||||
| chrX:2765041
|
CAAAAAAA others(2): Show |
C | 1 | a0001c0001t0002g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.62-5493_62-5485del others(9): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765041 | |||||
| chrX:2765057
|
A | AG | 26 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0115others(23): Show | 26 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.62-5493_62-5492ins others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765057 | ||||||
| chrX:2765057
|
A | G | 1 | a0001c0001t0026g0210 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.62-5493A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765057 | ||||||
| chrX:2765124
|
G | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0037others(60): Show | 64 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.62-5426G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765124 | ||||||
| chrX:2765125
|
A | G | 1 | a0001c0001t0002g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.62-5425A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765125 | ||||||
| chrX:2765152
|
C | G | 269 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0018others(266): Show | 269 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.62-5398C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765152 | ||||||
| chrX:2765156
|
G | A | 2 | a0001c0001t0001g0290a0001c0001t0009g0031 | 2 | NA18967.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.62-5394G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765156 | ||||||
| chrX:2765183
|
TA | T | 1 | a0001c0001t0004g0318 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.62-5362delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765183 | |||||
| chrX:2765185
|
A | C | 54 | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0001g0087others(51): Show | 54 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.62-5365A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765185 | ||||||
| chrX:2765189
|
TA | T | 6 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0085others(3): Show | 6 | HG02572.hp2 HG03130.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-5353delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765189 | |||||
| chrX:2765191
|
A | C | 32 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0032others(29): Show | 32 | HG00741.hp1 HG01074.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.62-5359A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765191 | ||||||
| chrX:2765192
|
A | C | 5 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0005g0046others(2): Show | 5 | HG02572.hp2 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-5358A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765192 | ||||||
| chrX:2765195
|
A | T | 1 | a0001c0001t0001g0090 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.62-5355A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765195 | ||||||
| chrX:2765200
|
A | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(258): Show | 262 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.62-5350A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765200 | ||||||
| chrX:2765220
|
G | A | 45 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0139others(42): Show | 45 | HG00140.hp1 HG00741.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.62-5330G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765220 | ||||||
| chrX:2765257
|
G | A | 236 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(233): Show | 236 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.62-5293G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765257 | ||||||
| chrX:2765272
|
AC | A | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-5276delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765272 | |||||
| chrX:2765278
|
G | C | 1 | a0001c0001t0001g0264 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.62-5272G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765278 | ||||||
| chrX:2765283
|
A | G | 82 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(79): Show | 82 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.62-5267A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765283 | ||||||
| chrX:2765308
|
GC | G | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-5240delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765308 | |||||
| chrX:2765325
|
TG | T | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-5222delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765325 | |||||
| chrX:2765365
|
A | G | 5 | a0001c0001t0013g0303a0001c0001t0013g0307a0001c0001t0019g0188others(2): Show | 5 | HG02486.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-5185A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765365 | ||||||
| chrX:2765372
|
GGGAGGGA others(5): Show |
G | 5 | a0001c0001t0013g0303a0001c0001t0013g0307a0001c0001t0019g0188others(2): Show | 5 | HG02486.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-5174_62-5163del others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765372 | |||||
| chrX:2765376
|
G | GGGAA | 29 | a0001c0001t0001g0032a0001c0001t0001g0107a0001c0001t0001g0139others(26): Show | 29 | HG00423.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.62-5137_62-5134dup others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | |||||
| chrX:2765376
|
G | GGGAAGGA others(1): Show |
41 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0043others(38): Show | 41 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.62-5141_62-5134dup others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | |||||
| chrX:2765376
|
G | GGGAAGGA others(5): Show |
6 | a0001c0001t0002g0108a0001c0001t0003g0100a0001c0001t0003g0250others(3): Show | 6 | HG00408.hp1 HG02970.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-5145_62-5134dup others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | |||||
| chrX:2765376
|
G | GGGAAGGA others(9): Show |
4 | a0001c0001t0003g0047a0001c0001t0003g0094a0001c0001t0013g0309others(1): Show | 4 | HG01884.hp1 HG04204.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-5149_62-5134dup others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | |||||
| chrX:2765376
|
G | GGGAAGGA others(13): Show |
6 | a0001c0001t0003g0048a0001c0001t0005g0046a0001c0001t0005g0288others(3): Show | 6 | HG01891.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-5153_62-5134dup others(20): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | |||||
| chrX:2765376
|
G | GGGAAGGA others(17): Show |
6 | a0001c0001t0002g0151a0001c0001t0003g0283a0001c0001t0010g0177others(3): Show | 6 | HG00140.hp1 HG00741.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-5157_62-5134dup others(24): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | |||||
| chrX:2765376
|
G | GGGAAGGA others(21): Show |
2 | a0001c0001t0001g0249a0001c0001t0010g0050 | 2 | HG02602.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.62-5161_62-5134dup others(28): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | |||||
| chrX:2765376
|
G | GGGAAGGA others(25): Show |
1 | a0001c0001t0011g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.62-5165_62-5134dup others(32): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | |||||
| chrX:2765376
|
GGGAA | G | 11 | a0001c0001t0001g0142a0001c0001t0001g0183a0001c0001t0002g0149others(8): Show | 11 | HG01099.hp1 HG01175.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.62-5137_62-5134del others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | |||||
| chrX:2765376
|
GGGAAGGA others(1): Show |
G | 163 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0023others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.62-5141_62-5134del others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | |||||
| chrX:2765401
|
G | GGAAGGAA others(4): Show |
1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-5147_62-5137dup others(11): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765401 | |||||
| chrX:2765452
|
C | T | 3 | a0001c0001t0001g0135a0001c0001t0001g0186a0001c0001t0001g0273 | 3 | HG01516.hp1 HG01517.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.62-5098C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765452 | ||||||
| chrX:2765491
|
G | C | 2 | a0001c0001t0001g0142a0001c0002t0044g0035 | 2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.62-5059G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765491 | ||||||
| chrX:2765518
|
T | C | 19 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0139others(16): Show | 19 | HG00741.hp1 HG01074.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.62-5032T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765518 | ||||||
| chrX:2765541
|
T | C | 4 | a0001c0001t0013g0309a0001c0001t0021g0278a0001c0002t0007g0052others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-5009T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765541 | ||||||
| chrX:2765561
|
TG | T | 1 | a0001c0001t0001g0032 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.62-4987delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765561 | |||||
| chrX:2765616
|
C | T | 1 | a0001c0001t0016g0277 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.62-4934C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765616 | ||||||
| chrX:2765654
|
TG | T | 1 | a0001c0001t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.62-4893delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765654 | |||||
| chrX:2765656
|
G | GC | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-4894_62-4893ins others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765656 | ||||||
| chrX:2765755
|
T | C | 1 | a0001c0001t0001g0014 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.62-4795T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765755 | ||||||
| chrX:2765769
|
A | G | 148 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(145): Show | 148 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.62-4781A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765769 | ||||||
| chrX:2765796
|
C | CATT | 24 | a0001c0001t0001g0093a0001c0001t0001g0249a0001c0001t0002g0151others(21): Show | 24 | HG00140.hp1 HG00741.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.62-4747_62-4745dup others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765796 | |||||
| chrX:2765863
|
G | GGGGTCGT | 1 | a0001c0001t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.62-4684_62-4678dup others(7): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765863 | |||||
| chrX:2765867
|
T | A | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.62-4683T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765867 | ||||||
| chrX:2765868
|
C | T | 1 | a0001c0001t0024g0184 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.62-4682C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765868 | ||||||
| chrX:2766095
|
T | TG | 1 | a0001c0001t0001g0032 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.62-4451dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766095 | |||||
| chrX:2766150
|
C | CT | 37 | a0001c0001t0001g0135a0001c0001t0001g0186a0001c0001t0001g0196others(34): Show | 37 | HG00323.hp1 HG00423.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.62-4391dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766150 | |||||
| chrX:2766150
|
CT | C | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-4391delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766150 | |||||
| chrX:2766176
|
C | G | 92 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0041others(89): Show | 92 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.62-4374C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766176 | ||||||
| chrX:2766222
|
T | C | 2 | a0001c0001t0004g0092a0001c0001t0017g0263 | 2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.62-4328T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766222 | ||||||
| chrX:2766273
|
TG | T | 1 | a0001c0001t0001g0032 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.62-4274delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766273 | |||||
| chrX:2766278
|
T | C | 1 | a0001c0001t0013g0309 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.62-4272T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766278 | ||||||
| chrX:2766287
|
C | T | 90 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0041others(87): Show | 90 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.62-4263C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766287 | ||||||
| chrX:2766288
|
G | A | 1 | a0001c0001t0003g0253 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.62-4262G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766288 | ||||||
| chrX:2766382
|
G | A | 5 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0005g0046others(2): Show | 5 | HG02572.hp2 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-4168G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766382 | ||||||
| chrX:2766395
|
TC | T | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-4152delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766395 | |||||
| chrX:2766423
|
GC | G | 1 | a0001c0001t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.62-4125delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766423 | |||||
| chrX:2766445
|
TG | T | 1 | a0001c0001t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.62-4103delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766445 | |||||
| chrX:2766486
|
TG | T | 1 | a0001c0001t0001g0032 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.62-4061delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766486 | |||||
| chrX:2766503
|
TG | T | 191 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(188): Show | 191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.62-4041delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766503 | |||||
| chrX:2766551
|
T | A | 2 | a0001c0001t0016g0293a0001c0001t0043g0255 | 2 | NA18941.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.62-3999T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766551 | ||||||
| chrX:2766557
|
C | CT | 13 | a0001c0001t0001g0023a0001c0001t0001g0056a0001c0001t0001g0114others(10): Show | 13 | HG01106.hp1 HG02074.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-3969dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766557 | |||||
| chrX:2766557
|
CT | C | 12 | a0001c0001t0001g0102a0001c0001t0001g0232a0001c0001t0001g0249others(9): Show | 12 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.62-3969delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766557 | |||||
| chrX:2766557
|
CTT | C | 3 | a0001c0001t0005g0288a0001c0001t0020g0131a0001c0002t0007g0276 | 3 | HG01891.hp1 HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.62-3970_62-3969del others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766557 | |||||
| chrX:2766557
|
CTTT | C | 8 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0005g0046others(5): Show | 8 | HG00741.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.62-3971_62-3969del others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766557 | |||||
| chrX:2766557
|
CTTTT | C | 77 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0032others(74): Show | 77 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.62-3972_62-3969del others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766557 | |||||
| chrX:2766557
|
CTTTTT | C | 125 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0043others(122): Show | 125 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.62-3973_62-3969del others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766557 | |||||
| chrX:2766557
|
CTTTTTT | C | 2 | a0001c0001t0001g0228a0001c0001t0003g0147 | 2 | NA19087.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.62-3974_62-3969del others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766557 | |||||
| chrX:2766557
|
CTTTTTTT | C | 1 | a0001c0001t0002g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.62-3975_62-3969del others(7): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766557 | |||||
| chrX:2766557
|
CTTTTTTT others(4): Show |
C | 1 | a0002c0008t0037g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.62-3979_62-3969del others(11): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766557 | |||||
| chrX:2766604
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.62-3946A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766604 | ||||||
| chrX:2766617
|
T | G | 1 | a0001c0001t0001g0216 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.62-3933T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766617 | ||||||
| chrX:2766619
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.62-3931T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766619 | ||||||
| chrX:2766620
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.62-3930A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766620 | ||||||
| chrX:2766621
|
C | G | 8 | a0001c0001t0001g0216a0001c0001t0001g0249a0001c0001t0002g0151others(5): Show | 8 | HG00140.hp1 HG00423.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-3929C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766621 | ||||||
| chrX:2766630
|
A | T | 6 | a0001c0001t0001g0214a0001c0001t0001g0216a0001c0001t0001g0304others(3): Show | 6 | HG00423.hp2 HG02145.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-3920A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766630 | ||||||
| chrX:2766658
|
G | A | 206 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(203): Show | 206 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.62-3892G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766658 | ||||||
| chrX:2766697
|
T | TG | 1 | a0001c0001t0001g0032 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.62-3850dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766697 | |||||
| chrX:2766712
|
C | G | 1 | a0001c0001t0009g0246 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.62-3838C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766712 | ||||||
| chrX:2766713
|
C | T | 1 | a0001c0001t0002g0217 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.62-3837C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766713 | ||||||
| chrX:2766714
|
G | A | 15 | a0001c0001t0001g0139a0001c0001t0001g0304a0001c0001t0003g0236others(12): Show | 15 | HG00741.hp1 HG01074.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.62-3836G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766714 | ||||||
| chrX:2766722
|
A | G | 1 | a0001c0001t0002g0217 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.62-3828A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766722 | ||||||
| chrX:2766725
|
C | T | 15 | a0001c0001t0001g0214a0001c0001t0001g0249a0001c0001t0002g0151others(12): Show | 15 | HG00140.hp1 HG00741.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.62-3825C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766725 | ||||||
| chrX:2766748
|
C | G | 227 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(224): Show | 227 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.62-3802C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766748 | ||||||
| chrX:2766756
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.62-3794G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766756 | ||||||
| chrX:2766782
|
G | A | 1 | a0001c0001t0006g0062 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.62-3768G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766782 | ||||||
| chrX:2766801
|
G | A | 11 | a0001c0001t0001g0249a0001c0001t0002g0151a0001c0001t0010g0050others(8): Show | 11 | HG00140.hp1 HG00741.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.62-3749G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766801 | ||||||
| chrX:2766811
|
T | C | 1 | a0001c0001t0001g0298 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.62-3739T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766811 | ||||||
| chrX:2766838
|
T | G | 1 | a0001c0001t0004g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.62-3712T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766838 | ||||||
| chrX:2766854
|
C | T | 6 | a0001c0001t0005g0003a0001c0001t0005g0020a0001c0001t0021g0021others(3): Show | 6 | HG01261.hp1 HG02630.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-3696C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766854 | ||||||
| chrX:2766861
|
A | G | 6 | a0001c0001t0022g0004a0001c0001t0023g0005a0001c0001t0023g0006others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-3689A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766861 | ||||||
| chrX:2766887
|
G | A | 2 | a0001c0001t0016g0293a0001c0001t0043g0255 | 2 | NA18941.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.62-3663G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766887 | ||||||
| chrX:2766935
|
CG | C | 1 | a0001c0001t0001g0032 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.62-3609delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766935 | |||||
| chrX:2767029
|
TG | T | 1 | a0001c0001t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.62-3516delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2767029 | |||||
| chrX:2767068
|
AG | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0037others(29): Show | 33 | HG00099.hp2 HG00544.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.62-3480delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2767068 | |||||
| chrX:2767094
|
C | T | 12 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0139others(9): Show | 12 | HG00741.hp1 HG01074.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.62-3456C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767094 | ||||||
| chrX:2767106
|
G | A | 107 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(104): Show | 107 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.62-3444G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767106 | ||||||
| chrX:2767152
|
G | A | 12 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0139others(9): Show | 12 | HG00741.hp1 HG01074.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.62-3398G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767152 | ||||||
| chrX:2767194
|
G | A | 2 | a0001c0001t0003g0033a0001c0001t0003g0236 | 2 | NA18982.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.62-3356G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767194 | ||||||
| chrX:2767213
|
T | C | 214 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(211): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.62-3337T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767213 | ||||||
| chrX:2767219
|
AG | A | 1 | a0001c0001t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.62-3327delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2767219 | |||||
| chrX:2767220
|
G | A | 211 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(208): Show | 211 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.62-3330G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767220 | ||||||
| chrX:2767278
|
T | A | 3 | a0001c0001t0022g0004a0001c0001t0023g0005a0001c0001t0023g0006 | 3 | HG01070.hp2 HG01071.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.62-3272T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767278 | ||||||
| chrX:2767317
|
A | T | 3 | a0001c0001t0022g0004a0001c0001t0023g0005a0001c0001t0023g0006 | 3 | HG01070.hp2 HG01071.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.62-3233A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767317 | ||||||
| chrX:2767331
|
G | GC | 1 | a0001c0001t0001g0032 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.62-3216dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2767331 | |||||
| chrX:2767378
|
GC | G | 1 | a0001c0001t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.62-3170delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2767378 | |||||
| chrX:2767387
|
C | T | 1 | a0001c0001t0002g0314 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.62-3163C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767387 | ||||||
| chrX:2767516
|
T | C | 1 | a0001c0002t0007g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.62-3034T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767516 | ||||||
| chrX:2767594
|
C | G | 1 | a0001c0002t0005g0275 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.62-2956C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767594 | ||||||
| chrX:2767657
|
G | T | 2 | a0001c0001t0001g0205a0001c0001t0002g0272 | 2 | HG00323.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.62-2893G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767657 | ||||||
| chrX:2767709
|
TG | T | 1 | a0001c0001t0001g0032 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.62-2839delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2767709 | |||||
| chrX:2767767
|
G | A | 98 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0041others(95): Show | 98 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.62-2783G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767767 | ||||||
| chrX:2767810
|
C | T | 5 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0259others(2): Show | 5 | HG01099.hp1 HG01175.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-2740C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767810 | ||||||
| chrX:2767818
|
G | A | 1 | a0001c0001t0003g0137 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.62-2732G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767818 | ||||||
| chrX:2767823
|
GT | G | 1 | a0001c0001t0001g0032 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.62-2724delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2767823 | |||||
| chrX:2767869
|
G | GC | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-2681_62-2680ins others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767869 | ||||||
| chrX:2767880
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | NA18968.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.62-2670G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767880 | ||||||
| chrX:2767906
|
AC | A | 1 | a0001c0001t0001g0032 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.62-2640delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2767906 | |||||
| chrX:2767966
|
AC | A | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-2579delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2767966 | |||||
| chrX:2768048
|
G | A | 1 | a0001c0001t0002g0179 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.62-2502G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768048 | ||||||
| chrX:2768078
|
C | T | 60 | a0001c0001t0001g0087a0001c0001t0001g0099a0001c0001t0001g0134others(57): Show | 60 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.62-2472C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768078 | ||||||
| chrX:2768079
|
C | T | 3 | a0001c0001t0007g0064a0001c0001t0022g0191a0002c0003t0001g0028 | 3 | HG02451.hp2 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.62-2471C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768079 | ||||||
| chrX:2768124
|
A | G | 60 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0099others(57): Show | 60 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.62-2426A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768124 | ||||||
| chrX:2768233
|
G | C | 1 | a0001c0002t0008g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.62-2317G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768233 | ||||||
| chrX:2768248
|
G | GA | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-2302_62-2301ins others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768248 | ||||||
| chrX:2768257
|
TA | T | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-2291delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2768257 | |||||
| chrX:2768261
|
A | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | NA18946.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.62-2289A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768261 | ||||||
| chrX:2768279
|
C | T | 1 | a0001c0001t0005g0022 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.62-2271C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768279 | ||||||
| chrX:2768320
|
T | TA | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-2230_62-2229ins others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768320 | ||||||
| chrX:2768461
|
C | T | 100 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0043others(97): Show | 100 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.62-2089C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768461 | ||||||
| chrX:2768475
|
G | T | 8 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0095others(5): Show | 8 | HG00673.hp1 NA18944.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-2075G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768475 | ||||||
| chrX:2768525
|
TG | T | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-2022delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2768525 | |||||
| chrX:2768545
|
G | A | 94 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0043others(91): Show | 94 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.62-2005G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768545 | ||||||
| chrX:2768589
|
G | GA | 1 | a0001c0001t0001g0032 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.62-1958dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2768589 | |||||
| chrX:2768606
|
G | GA | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-1940dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2768606 | |||||
| chrX:2768624
|
TG | T | 2 | a0001c0001t0001g0032a0001c0001t0004g0167 | 2 | HG01169.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.62-1923delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2768624 | |||||
| chrX:2768682
|
C | T | 2 | a0001c0001t0001g0196a0001c0001t0004g0146 | 2 | NA18946.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.62-1868C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768682 | ||||||
| chrX:2768706
|
T | TGA | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-1843_62-1842ins others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2768706 | |||||
| chrX:2768732
|
C | A | 1 | a0001c0002t0007g0052 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.62-1818C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768732 | ||||||
| chrX:2768812
|
GA | G | 1 | a0001c0001t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.62-1736delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2768812 | |||||
| chrX:2768825
|
T | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0041others(151): Show | 155 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.62-1725T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768825 | ||||||
| chrX:2768850
|
C | G | 1 | a0001c0001t0003g0158 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.62-1700C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768850 | ||||||
| chrX:2768858
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.62-1692C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768858 | ||||||
| chrX:2768921
|
GT | G | 1 | a0001c0001t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.62-1626delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2768921 | |||||
| chrX:2768945
|
A | AT | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-1602dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2768945 | |||||
| chrX:2769087
|
C | T | 1 | a0001c0001t0005g0022 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.62-1463C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2769087 | ||||||
| chrX:2769099
|
C | CGG | 1 | a0001c0007t0032g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.62-1450_62-1449dup others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2769099 | |||||
| chrX:2769143
|
C | CG | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-1404dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2769143 | |||||
| chrX:2769267
|
CG | C | 1 | a0001c0001t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.62-1278delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2769267 | |||||
| chrX:2769268
|
G | A | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0005g0046others(6): Show | 9 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-1282G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2769268 | ||||||
| chrX:2769281
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(213): Show | 217 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.62-1269T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2769281 | ||||||
| chrX:2769399
|
A | T | 1 | a0001c0002t0008g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.62-1151A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2769399 | ||||||
| chrX:2769403
|
TC | T | 1 | a0001c0001t0004g0318 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.62-1144delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2769403 | |||||
| chrX:2769422
|
TC | T | 1 | a0001c0001t0001g0032 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.62-1126delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2769422 | |||||
| chrX:2769517
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0041others(153): Show | 157 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.62-1033A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2769517 | ||||||
| chrX:2769531
|
C | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0057others(53): Show | 57 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.62-1019C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2769531 | ||||||
| chrX:2769633
|
AG | A | 1 | a0001c0002t0005g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.62-915delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2769633 | |||||
| chrX:2769852
|
GC | G | 1 | a0001c0001t0030g0091 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.62-693delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2769852 | |||||
| chrX:2769857
|
C | CA | 1 | a0001c0001t0001g0016 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.62-690dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2769857 | |||||
| chrX:2769879
|
T | C | 1 | a0001c0001t0004g0160 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.62-671T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2769879 | ||||||
| chrX:2769887
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.62-663G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2769887 | ||||||
| chrX:2769919
|
A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0005g0046others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-631A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2769919 | ||||||
| chrX:2769986
|
GC | G | 1 | a0001c0001t0001g0105 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.62-560delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2769986 | |||||
| chrX:2770014
|
T | TG | 1 | a0001c0001t0001g0001 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.62-535dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2770014 | |||||
| chrX:2770014
|
TGTGGA | T | 1 | a0002c0003t0008g0066 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.62-534_62-530delTG others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2770014 | |||||
| chrX:2770014
|
TGTGGAG | T | 2 | a0001c0001t0001g0093a0002c0003t0008g0065 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.62-534_62-529delTG others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2770014 | |||||
| chrX:2770016
|
T | G | 1 | a0001c0001t0001g0001 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.62-534T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770016 | ||||||
| chrX:2770016
|
T | TC | 1 | a0001c0002t0005g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.62-534_62-533insC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770016 | ||||||
| chrX:2770016
|
T | TG | 1 | a0001c0001t0001g0273 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.62-532dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2770016 | |||||
| chrX:2770016
|
TGGA | T | 4 | a0001c0001t0001g0095a0001c0001t0004g0185a0001c0001t0006g0017others(1): Show | 4 | HG02683.hp2 HG02735.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-531_62-529delAG others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2770016 | |||||
| chrX:2770017
|
G | C | 3 | a0001c0001t0007g0064a0001c0001t0022g0191a0002c0003t0001g0028 | 3 | HG02451.hp2 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.62-533G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770017 | ||||||
| chrX:2770017
|
GGA | G | 14 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0069others(11): Show | 14 | HG00280.hp1 HG00673.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.62-531_62-530delAG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2770017 | |||||
| chrX:2770018
|
GA | G | 24 | a0001c0001t0001g0071a0001c0001t0001g0089a0001c0001t0001g0090others(21): Show | 24 | HG00621.hp1 HG01192.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.62-531delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770018 | ||||||
| chrX:2770019
|
A | C | 1 | a0001c0001t0001g0238 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.62-531A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770019 | ||||||
| chrX:2770019
|
A | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0086a0001c0001t0001g0265others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.62-531A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770019 | ||||||
| chrX:2770023
|
G | T | 1 | a0001c0001t0016g0277 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.62-527G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770023 | ||||||
| chrX:2770023
|
GT | G | 1 | a0001c0001t0001g0238 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.62-526delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770023 | ||||||
| chrX:2770024
|
T | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0057others(52): Show | 56 | HG00280.hp1 HG00621.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.62-526T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770024 | ||||||
| chrX:2770024
|
T | TG | 7 | a0001c0001t0001g0083a0001c0001t0001g0212a0001c0001t0003g0137others(4): Show | 7 | HG02055.hp1 HG03704.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-518dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2770024 | |||||
| chrX:2770036
|
TG | T | 1 | a0001c0001t0030g0091 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.62-508delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2770036 | |||||
| chrX:2770149
|
G | C | 1 | a0002c0003t0008g0066 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.62-401G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770149 | ||||||
| chrX:2770248
|
A | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0023others(156): Show | 160 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.62-302A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770248 | ||||||
| chrX:2770293
|
T | TG | 1 | a0001c0001t0001g0105 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.62-255dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2770293 | |||||
| chrX:2770405
|
TC | T | 1 | a0001c0001t0001g0016 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.62-142delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2770405 | |||||
| chrX:2770410
|
T | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0023others(163): Show | 167 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.62-140T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770410 | ||||||
| chrX:2770501
|
T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0023others(162): Show | 166 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.62-49T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770501 | ||||||
| chrX:2770519
|
G | GT | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-31_62-30insT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770519 | ||||||
| chrX:2770687
|
TG | T | 1 | a0001c0001t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.103+99delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2770687 | |||||
| chrX:2770797
|
GTGC | G | 1 | a0001c0001t0003g0219 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.103+208_103+210del others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2770797 | |||||
| chrX:2770825
|
T | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0057others(51): Show | 55 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.103+234T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2770825 | ||||||
| chrX:2770918
|
T | C | 89 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0041others(86): Show | 89 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.103+327T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2770918 | ||||||
| chrX:2770996
|
G | GC | 1 | a0001c0001t0003g0219 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.103+410dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2770996 | |||||
| chrX:2771005
|
C | G | 1 | a0001c0001t0013g0309 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.103+414C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771005 | ||||||
| chrX:2771013
|
AT | A | 1 | a0001c0001t0003g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.103+429delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2771013 | |||||
| chrX:2771015
|
T | C | 1 | a0001c0001t0009g0246 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.103+424T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771015 | ||||||
| chrX:2771015
|
T | G | 1 | a0001c0001t0003g0039 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.103+424T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771015 | ||||||
| chrX:2771038
|
GA | G | 1 | a0001c0001t0003g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.103+450delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2771038 | |||||
| chrX:2771081
|
TG | T | 1 | a0001c0001t0001g0105 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.103+493delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2771081 | |||||
| chrX:2771109
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.103+518T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771109 | ||||||
| chrX:2771196
|
T | TC | 1 | a0001c0001t0003g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.103+608dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2771196 | |||||
| chrX:2771201
|
CACCCCGA others(74): Show |
C | 1 | a0004c0009t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.103+645_103+725del others(81): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2771201 | |||||
| chrX:2771209
|
TC | T | 1 | a0001c0001t0003g0219 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.103+621delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2771209 | |||||
| chrX:2771224
|
TC | T | 1 | a0001c0001t0003g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.103+635delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2771224 | |||||
| chrX:2771239
|
T | TTC | 1 | a0001c0001t0003g0219 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.103+650_103+651dup others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2771239 | |||||
| chrX:2771259
|
A | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(165): Show | 169 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.103+668A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771259 | ||||||
| chrX:2771283
|
A | AC | 1 | a0001c0001t0004g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.103+696dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2771283 | |||||
| chrX:2771312
|
TC | T | 1 | a0001c0001t0003g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.103+725delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2771312 | |||||
| chrX:2771342
|
T | TC | 2 | a0001c0001t0004g0111a0001c0001t0004g0127 | 2 | NA18989.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.103+755dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2771342 | |||||
| chrX:2771342
|
TC | T | 1 | a0001c0001t0018g0200 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.103+755delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2771342 | |||||
| chrX:2771493
|
T | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(168): Show | 172 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.103+902T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771493 | ||||||
| chrX:2771499
|
G | GC | 1 | a0001c0001t0003g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.103+911dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2771499 | |||||
| chrX:2771534
|
G | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(175): Show | 179 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.103+943G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771534 | ||||||
| chrX:2771560
|
G | A | 3 | a0001c0001t0001g0304a0001c0001t0005g0305a0001c0001t0005g0306 | 3 | HG02258.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.103+969G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771560 | ||||||
| chrX:2771566
|
G | A | 72 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0041others(69): Show | 72 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.103+975G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771566 | ||||||
| chrX:2771568
|
TG | T | 2 | a0001c0001t0003g0120a0001c0001t0003g0219 | 2 | NA19058.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.103+980delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2771568 | |||||
| chrX:2771589
|
G | C | 1 | a0001c0001t0001g0261 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.103+998G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771589 | ||||||
| chrX:2771595
|
G | A | 3 | a0001c0001t0001g0304a0001c0001t0005g0305a0001c0001t0005g0306 | 3 | HG02258.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.103+1004G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771595 | ||||||
| chrX:2771638
|
TA | T | 1 | a0001c0001t0003g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.103+1050delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2771638 | |||||
| chrX:2771775
|
CA | C | 1 | a0001c0001t0003g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.103+1186delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2771775 | |||||
| chrX:2771782
|
A | G | 46 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0041others(43): Show | 46 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.103+1191A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771782 | ||||||
| chrX:2771845
|
A | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(176): Show | 180 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.103+1254A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771845 | ||||||
| chrX:2771895
|
A | ACC | 1 | a0001c0001t0003g0219 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.103+1307_103+1308d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2771895 | |||||
| chrX:2771912
|
C | T | 3 | a0001c0001t0001g0304a0001c0001t0005g0305a0001c0001t0005g0306 | 3 | HG02258.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.103+1321C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771912 | ||||||
| chrX:2772070
|
T | TG | 1 | a0001c0001t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.103+1481dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2772070 | |||||
| chrX:2772222
|
C | G | 1 | a0001c0001t0003g0176 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.103+1631C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772222 | ||||||
| chrX:2772233
|
TG | T | 1 | a0001c0001t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.103+1645delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2772233 | |||||
| chrX:2772242
|
G | T | 1 | a0001c0001t0001g0260 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.103+1651G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772242 | ||||||
| chrX:2772269
|
T | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(168): Show | 172 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.103+1678T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772269 | ||||||
| chrX:2772270
|
G | GT | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.103+1682dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2772270 | |||||
| chrX:2772360
|
C | G | 68 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(65): Show | 69 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.103+1769C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772360 | ||||||
| chrX:2772405
|
G | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0057others(50): Show | 54 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.103+1814G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772405 | ||||||
| chrX:2772410
|
G | A | 3 | a0001c0001t0001g0304a0001c0001t0005g0305a0001c0001t0005g0306 | 3 | HG02258.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.103+1819G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772410 | ||||||
| chrX:2772513
|
CAG | C | 1 | a0001c0001t0003g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.103+1928_103+1929d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2772513 | |||||
| chrX:2772599
|
TG | T | 1 | a0001c0001t0018g0199 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.103+2014delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2772599 | |||||
| chrX:2772721
|
AT | A | 1 | a0001c0001t0018g0200 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.104-1989delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2772721 | |||||
| chrX:2772727
|
T | TA | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.104-1984dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2772727 | |||||
| chrX:2772773
|
T | C | 1 | a0002c0008t0037g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.104-1943T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772773 | ||||||
| chrX:2772786
|
C | G | 11 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0304others(8): Show | 11 | HG02145.hp1 HG02258.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.104-1930C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772786 | ||||||
| chrX:2772880
|
C | A | 3 | a0001c0001t0010g0177a0003c0004t0001g0226a0003c0004t0001g0227 | 3 | HG00140.hp1 HG01361.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.104-1836C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772880 | ||||||
| chrX:2772881
|
C | G | 3 | a0001c0001t0010g0177a0003c0004t0001g0226a0003c0004t0001g0227 | 3 | HG00140.hp1 HG01361.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.104-1835C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772881 | ||||||
| chrX:2772958
|
CT | C | 1 | a0001c0001t0001g0032 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.104-1754delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2772958 | |||||
| chrX:2772967
|
G | C | 17 | a0001c0001t0001g0001a0001c0001t0001g0093a0001c0001t0001g0214others(14): Show | 18 | HG00423.hp2 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.104-1749G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772967 | ||||||
| chrX:2772971
|
A | G | 1 | a0001c0001t0011g0208 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.104-1745A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772971 | ||||||
| chrX:2773015
|
TA | T | 1 | a0001c0001t0030g0091 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.104-1695delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773015 | |||||
| chrX:2773023
|
A | C | 83 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0041others(80): Show | 83 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.104-1693A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773023 | ||||||
| chrX:2773048
|
G | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(172): Show | 176 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.104-1668G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773048 | ||||||
| chrX:2773116
|
GA | G | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.104-1598delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773116 | |||||
| chrX:2773157
|
C | CAGGG | 1 | a0001c0001t0024g0184 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.104-1547_104-1544d others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773157 | |||||
| chrX:2773179
|
G | T | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.104-1537G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773179 | ||||||
| chrX:2773188
|
A | G | 1 | a0001c0001t0013g0309 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.104-1528A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773188 | ||||||
| chrX:2773235
|
G | A | 8 | a0001c0001t0007g0064a0001c0001t0010g0193a0001c0001t0022g0191others(5): Show | 8 | HG02451.hp2 HG02647.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-1481G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773235 | ||||||
| chrX:2773285
|
A | AAGGAGGG others(1): Show |
1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1431_104-1430i others(10): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773285 | ||||||
| chrX:2773288
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1428A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773288 | ||||||
| chrX:2773295
|
T | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1421T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773295 | ||||||
| chrX:2773299
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1417G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773299 | ||||||
| chrX:2773302
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1414G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773302 | ||||||
| chrX:2773309
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1407A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773309 | ||||||
| chrX:2773310
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1406A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773310 | ||||||
| chrX:2773311
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1405G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773311 | ||||||
| chrX:2773317
|
A | AG | 2 | a0001c0001t0001g0016a0001c0001t0001g0224 | 2 | NA19075.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.104-1393dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773317 | |||||
| chrX:2773318
|
G | GA | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1398_104-1397i others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773318 | ||||||
| chrX:2773320
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1396G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773320 | ||||||
| chrX:2773330
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1386A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773330 | ||||||
| chrX:2773334
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1382A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773334 | ||||||
| chrX:2773338
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1378A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773338 | ||||||
| chrX:2773339
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1377A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773339 | ||||||
| chrX:2773341
|
T | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1375T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773341 | ||||||
| chrX:2773342
|
A | G | 114 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0037others(111): Show | 114 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.104-1374A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773342 | ||||||
| chrX:2773343
|
G | GA | 1 | a0001c0001t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.104-1373_104-1372i others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773343 | ||||||
| chrX:2773344
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1372G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773344 | ||||||
| chrX:2773345
|
A | AG | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1370dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773345 | |||||
| chrX:2773350
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1366A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773350 | ||||||
| chrX:2773355
|
A | AG | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1361_104-1360i others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773355 | ||||||
| chrX:2773359
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1357A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773359 | ||||||
| chrX:2773360
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1356A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773360 | ||||||
| chrX:2773361
|
GA | G | 1 | a0001c0001t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.104-1350delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773361 | |||||
| chrX:2773363
|
A | AGG | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1353_104-1352i others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773363 | ||||||
| chrX:2773366
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1350A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773366 | ||||||
| chrX:2773369
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1347A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773369 | ||||||
| chrX:2773370
|
T | A | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1346T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773370 | ||||||
| chrX:2773371
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1345A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773371 | ||||||
| chrX:2773381
|
C | A | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1335C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773381 | ||||||
| chrX:2773385
|
G | GAGAA | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1331_104-1330i others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773385 | ||||||
| chrX:2773400
|
AG | A | 1 | a0001c0001t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.104-1313delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773400 | |||||
| chrX:2773404
|
A | AAGG | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1312_104-1311i others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773404 | ||||||
| chrX:2773405
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1311G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773405 | ||||||
| chrX:2773411
|
A | AG | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1305_104-1304i others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773411 | ||||||
| chrX:2773416
|
T | A | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1300T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773416 | ||||||
| chrX:2773417
|
T | A | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1299T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773417 | ||||||
| chrX:2773421
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1295G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773421 | ||||||
| chrX:2773424
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1292G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773424 | ||||||
| chrX:2773425
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1291A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773425 | ||||||
| chrX:2773426
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1290G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773426 | ||||||
| chrX:2773429
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1287A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773429 | ||||||
| chrX:2773435
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1281A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773435 | ||||||
| chrX:2773442
|
G | A | 2 | a0001c0001t0001g0162a0002c0003t0008g0065 | 2 | HG02976.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.104-1274G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773442 | ||||||
| chrX:2773444
|
T | A | 2 | a0001c0001t0001g0162a0002c0003t0008g0065 | 2 | HG02976.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.104-1272T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773444 | ||||||
| chrX:2773445
|
G | A | 2 | a0001c0001t0001g0162a0002c0003t0008g0065 | 2 | HG02976.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.104-1271G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773445 | ||||||
| chrX:2773448
|
G | A | 2 | a0001c0001t0001g0162a0002c0003t0008g0065 | 2 | HG02976.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.104-1268G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773448 | ||||||
| chrX:2773457
|
A | G | 2 | a0001c0001t0001g0162a0002c0003t0008g0065 | 2 | HG02976.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.104-1259A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773457 | ||||||
| chrX:2773458
|
A | G | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-1258A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773458 | ||||||
| chrX:2773458
|
AGAAGAAG others(21): Show |
A | 1 | a0002c0003t0008g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.104-1253_104-1226d others(30): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773458 | |||||
| chrX:2773461
|
A | AG | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1254dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773461 | |||||
| chrX:2773465
|
G | GGAA | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1250_104-1249i others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773465 | |||||
| chrX:2773468
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1248G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773468 | ||||||
| chrX:2773471
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1245A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773471 | ||||||
| chrX:2773477
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1239G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773477 | ||||||
| chrX:2773478
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1238A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773478 | ||||||
| chrX:2773481
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1235G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773481 | ||||||
| chrX:2773481
|
GGGAA | G | 6 | a0001c0001t0001g0287a0001c0001t0007g0064a0001c0001t0022g0191others(3): Show | 6 | HG00741.hp1 HG02451.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-1219_104-1216d others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773481 | |||||
| chrX:2773481
|
GGGAAGGA others(1): Show |
G | 1 | a0001c0002t0007g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.104-1223_104-1216d others(10): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773481 | |||||
| chrX:2773485
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1231A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773485 | ||||||
| chrX:2773486
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1230G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773486 | ||||||
| chrX:2773486
|
G | GGAAGGAA others(9): Show |
3 | a0001c0001t0002g0179a0001c0001t0004g0153a0001c0001t0005g0020 | 3 | HG02132.hp1 HG02273.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.104-1086_104-1071d others(18): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
G | GGAAGGAA others(25): Show |
3 | a0001c0001t0001g0231a0001c0001t0001g0298a0001c0001t0003g0240 | 3 | HG00609.hp1 HG01433.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.104-1102_104-1071d others(34): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
G | GGAAGGAA others(41): Show |
1 | a0001c0001t0002g0182 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.104-1118_104-1071d others(50): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
G | GGAAGGAA others(57): Show |
3 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0181 | 3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.104-1134_104-1071d others(66): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
G | GGAAGGAA others(137): Show |
1 | a0001c0001t0001g0252 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.104-1214_104-1071d others(146): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
G | GGAAGGAA others(184): Show |
1 | a0001c0001t0001g0019 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(193): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
G | GGAAGGAA others(953): Show |
1 | a0001c0001t0001g0086 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(962): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
G | GGAAGGAA others(497): Show |
1 | a0001c0001t0001g0196 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.104-1100_104-1099i others(506): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
G | GGAAGGAA others(73): Show |
1 | a0001c0002t0008g0321 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.104-1196_104-1195i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
G | GGAAGGAA others(81): Show |
1 | a0001c0001t0006g0080 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.104-1196_104-1195i others(90): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
G | GGAAGGAA others(89): Show |
1 | a0001c0001t0004g0245 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.104-1196_104-1195i others(98): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
G | GGAAGGAA others(105): Show |
1 | a0001c0001t0002g0217 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.104-1196_104-1195i others(114): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
G | GGAAGGAA others(121): Show |
1 | a0001c0001t0004g0222 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.104-1196_104-1195i others(130): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
G | GGAAGGAA others(137): Show |
1 | a0001c0001t0002g0156 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.104-1196_104-1195i others(146): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
G | GGAAGGAA others(85): Show |
1 | a0001c0002t0007g0276 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.104-1220_104-1219i others(94): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
G | GGAAGGAA others(293): Show |
1 | a0001c0001t0005g0288 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.104-1220_104-1219i others(302): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
G | GGAAGGAG others(105): Show |
1 | a0001c0002t0044g0035 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.104-1224_104-1223i others(114): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
GGAAGGAA others(9): Show |
G | 2 | a0001c0001t0001g0244a0001c0001t0039g0036 | 2 | HG00733.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.104-1086_104-1071d others(18): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
GGAAGGAA others(121): Show |
G | 2 | a0001c0001t0001g0001a0001c0001t0001g0273 | 3 | HG01069.hp2 HG01071.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.104-1198_104-1071d others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
GGAAGGAA others(153): Show |
G | 1 | a0001c0001t0004g0318 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.104-1118_104-959de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773486
|
GGAAGGAA others(185): Show |
G | 1 | a0003c0004t0002g0211 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.104-1150_104-959de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | |||||
| chrX:2773489
|
A | AGGAAGGA others(73): Show |
1 | a0001c0001t0004g0185 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.104-1196_104-1195i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773489 | |||||
| chrX:2773489
|
A | AGGAAGGA others(361): Show |
1 | a0001c0001t0001g0169 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.104-1196_104-1195i others(370): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773489 | |||||
| chrX:2773489
|
A | AGGAAGGA others(41): Show |
5 | a0001c0001t0001g0023a0001c0001t0001g0224a0001c0001t0001g0261others(2): Show | 5 | HG00423.hp1 NA18968.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-1196_104-1195i others(50): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773489 | |||||
| chrX:2773489
|
A | AGGAAGGA others(73): Show |
1 | a0001c0001t0003g0176 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.104-1196_104-1195i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773489 | |||||
| chrX:2773489
|
A | AGGAAGGA others(41): Show |
1 | a0001c0001t0003g0033 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.104-1212_104-1211i others(50): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773489 | |||||
| chrX:2773489
|
A | AGGAAGGA others(21): Show |
1 | a0001c0001t0003g0256 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.104-1220_104-1219i others(30): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773489 | |||||
| chrX:2773489
|
A | AGGAAGGA others(309): Show |
1 | a0001c0001t0001g0134 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.104-1220_104-1219i others(318): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773489 | |||||
| chrX:2773489
|
A | G | 1 | a0002c0003t0008g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.104-1227A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773489 | ||||||
| chrX:2773502
|
A | AGAAGGAA others(313): Show |
1 | a0001c0001t0002g0198 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(322): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773502 | |||||
| chrX:2773502
|
A | AGAAGGAA others(297): Show |
1 | a0001c0001t0016g0293 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(306): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773502 | |||||
| chrX:2773502
|
A | AGAAGGAA others(281): Show |
1 | a0001c0001t0043g0255 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(290): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773502 | |||||
| chrX:2773502
|
A | AGAAGGAA others(297): Show |
1 | a0001c0001t0001g0280 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.104-1196_104-1195i others(306): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773502 | |||||
| chrX:2773502
|
A | C | 2 | a0001c0001t0001g0015a0001c0001t0005g0288 | 2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.104-1214A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773502 | ||||||
| chrX:2773502
|
AGAAGGAA others(137): Show |
A | 1 | a0001c0001t0029g0059 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.104-1102_104-959de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773502 | |||||
| chrX:2773502
|
AGAAGGAA others(265): Show |
A | 1 | a0001c0001t0002g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.104-1135_104-864de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773502 | |||||
| chrX:2773505
|
A | AGGAAGGA others(73): Show |
2 | a0001c0001t0001g0175a0001c0001t0002g0174 | 2 | NA19054.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.104-1180_104-1179i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | |||||
| chrX:2773505
|
A | AGGAAGGA others(9): Show |
9 | a0001c0001t0001g0118a0001c0001t0001g0209a0001c0001t0002g0132others(6): Show | 9 | HG00597.hp2 HG00673.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.104-1196_104-1195i others(18): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | |||||
| chrX:2773505
|
A | AGGAAGGA others(89): Show |
1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1196_104-1195i others(98): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | |||||
| chrX:2773505
|
A | AGGAAGGA others(25): Show |
19 | a0001c0001t0001g0043a0001c0001t0001g0110a0001c0001t0001g0135others(16): Show | 19 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(16): Show |
intron_variant | MODIFIER | c.104-1196_104-1195i others(34): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | |||||
| chrX:2773505
|
A | AGGAAGGA others(57): Show |
14 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0159others(11): Show | 14 | HG00558.hp2 HG00597.hp1 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.104-1196_104-1195i others(66): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | |||||
| chrX:2773505
|
A | AGGAAGGA others(89): Show |
1 | a0001c0001t0002g0262 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.104-1196_104-1195i others(98): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | |||||
| chrX:2773505
|
A | AGGAAGGA others(185): Show |
1 | a0001c0001t0006g0165 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.104-1196_104-1195i others(194): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | |||||
| chrX:2773505
|
A | AGGAAGGA others(265): Show |
2 | a0001c0001t0004g0192a0001c0001t0006g0166 | 2 | HG02155.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.104-1196_104-1195i others(274): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | |||||
| chrX:2773505
|
A | AGGAAGGA others(233): Show |
1 | a0001c0001t0001g0099 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.104-1196_104-1195i others(242): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | |||||
| chrX:2773505
|
A | AGGAAGGA others(73): Show |
1 | a0001c0001t0001g0206 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.104-1196_104-1195i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | |||||
| chrX:2773505
|
A | AGGAAGGA others(57): Show |
2 | a0001c0001t0001g0163a0001c0001t0026g0171 | 2 | NA18950.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.104-1196_104-1195i others(66): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | |||||
| chrX:2773505
|
A | AGGAAGGA others(73): Show |
1 | a0001c0001t0001g0071 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.104-1196_104-1195i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | |||||
| chrX:2773505
|
A | AGGAAGGA others(89): Show |
3 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0103 | 3 | NA18944.hp2 NA18968.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.104-1196_104-1195i others(98): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | |||||
| chrX:2773505
|
A | AGGAAGGA others(233): Show |
1 | a0001c0001t0020g0138 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.104-1196_104-1195i others(242): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | |||||
| chrX:2773505
|
A | G | 4 | a0001c0001t0001g0134a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG01981.hp2 HG02559.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-1211A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773505 | ||||||
| chrX:2773508
|
A | AAGGAAGG others(152): Show |
1 | a0001c0001t0001g0018 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(161): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773508 | |||||
| chrX:2773518
|
A | AGAAGGAA others(409): Show |
1 | a0001c0001t0002g0239 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(418): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773518 | |||||
| chrX:2773518
|
A | AGAAGGAA others(297): Show |
1 | a0001c0001t0002g0272 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(306): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773518 | |||||
| chrX:2773518
|
A | AGAAGGAA others(633): Show |
1 | a0001c0001t0003g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.104-1119_104-1118i others(642): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773518 | |||||
| chrX:2773518
|
A | AGAAGGAA others(633): Show |
1 | a0001c0001t0003g0048 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.104-1119_104-1118i others(642): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773518 | |||||
| chrX:2773518
|
A | AGAAGGAA others(73): Show |
1 | a0001c0001t0020g0131 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.104-1135_104-1134i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773518 | |||||
| chrX:2773518
|
A | AGAGGGAA others(17): Show |
1 | a0001c0001t0001g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.104-1196_104-1195i others(26): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773518 | |||||
| chrX:2773518
|
A | C | 4 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0107others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-1198A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773518 | ||||||
| chrX:2773518
|
AGAAG | A | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.104-1187_104-1184d others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773518 | |||||
| chrX:2773518
|
AGAAGGAA others(121): Show |
A | 4 | a0001c0001t0002g0040a0001c0001t0006g0254a0001c0001t0010g0177others(1): Show | 4 | HG00733.hp2 HG02257.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-1086_104-959de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773518 | |||||
| chrX:2773518
|
AGAAGGAA others(249): Show |
A | 4 | a0001c0001t0001g0093a0001c0001t0017g0269a0001c0001t0025g0317others(1): Show | 4 | HG03516.hp1 NA19085.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-1119_104-864de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773518 | |||||
| chrX:2773521
|
A | AGGAAGGA others(57): Show |
1 | a0001c0001t0003g0250 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.104-1148_104-1147i others(66): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773521 | |||||
| chrX:2773521
|
A | AGGAAGGA others(521): Show |
1 | a0001c0001t0003g0076 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.104-1180_104-1179i others(530): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773521 | |||||
| chrX:2773521
|
A | AGGAAGGA others(41): Show |
1 | a0001c0001t0003g0148 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.104-1180_104-1179i others(50): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773521 | |||||
| chrX:2773521
|
A | AGGAAGGA others(73): Show |
2 | a0001c0001t0003g0024a0001c0001t0003g0120 | 2 | NA18971.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.104-1180_104-1179i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773521 | |||||
| chrX:2773521
|
A | AGGAAGGA others(25): Show |
2 | a0001c0001t0004g0126a0001c0001t0004g0127 | 2 | NA18961.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.104-1180_104-1179i others(34): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773521 | |||||
| chrX:2773521
|
A | AGGAAGGA others(89): Show |
1 | a0002c0003t0001g0042 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.104-1180_104-1179i others(98): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773521 | |||||
| chrX:2773521
|
A | G | 64 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0089others(61): Show | 64 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.104-1195A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773521 | ||||||
| chrX:2773534
|
A | AGAAGGAA others(233): Show |
1 | a0004c0009t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.104-1087_104-1086i others(242): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773534 | |||||
| chrX:2773534
|
A | AGAAGGAA others(409): Show |
1 | a0001c0001t0002g0067 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.104-1164_104-1163i others(418): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773534 | |||||
| chrX:2773534
|
A | AGAGGGAA others(1): Show |
3 | a0001c0001t0005g0119a0001c0002t0005g0128a0001c0005t0015g0045 | 3 | HG02109.hp1 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.104-1180_104-1179i others(10): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773534 | |||||
| chrX:2773534
|
A | C | 1 | a0001c0001t0001g0244 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.104-1182A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773534 | ||||||
| chrX:2773534
|
AGAAGGAA others(105): Show |
A | 11 | a0001c0001t0001g0032a0001c0001t0001g0107a0001c0001t0001g0212others(8): Show | 11 | HG01168.hp2 HG01169.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.104-1054_104-943de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773534 | |||||
| chrX:2773537
|
A | AGGAAGGA others(361): Show |
1 | a0001c0002t0005g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.104-1164_104-1163i others(370): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773537 | |||||
| chrX:2773537
|
A | G | 66 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0069others(63): Show | 66 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.104-1179A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773537 | ||||||
| chrX:2773547
|
G | GAGAGAAG others(1193): Show |
1 | a0001c0001t0001g0014 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.104-1116_104-1115i others(1202): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773547 | |||||
| chrX:2773550
|
A | AGAAGGAA others(265): Show |
1 | a0001c0001t0006g0075 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(274): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773550 | |||||
| chrX:2773550
|
A | AGAAGGAA others(233): Show |
1 | a0001c0001t0003g0253 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(242): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773550 | |||||
| chrX:2773550
|
A | AGAAGGAA others(265): Show |
1 | a0001c0001t0006g0025 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(274): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773550 | |||||
| chrX:2773550
|
AGAAGGAA others(89): Show |
A | 9 | a0001c0001t0001g0115a0001c0001t0001g0232a0001c0001t0001g0234others(6): Show | 9 | HG00140.hp1 HG01496.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.104-1070_104-975de others(97): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773550 | |||||
| chrX:2773550
|
AGAAGGAA others(217): Show |
A | 1 | a0001c0001t0024g0088 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.104-1087_104-864de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773550 | |||||
| chrX:2773553
|
A | AGGAAGGA others(197): Show |
1 | a0001c0001t0011g0208 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.104-1148_104-1147i others(206): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773553 | |||||
| chrX:2773553
|
A | AGGAAGGA others(41): Show |
1 | a0001c0001t0003g0201 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.104-1148_104-1147i others(50): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773553 | |||||
| chrX:2773553
|
A | G | 41 | a0001c0001t0001g0069a0001c0001t0001g0134a0001c0001t0001g0135others(38): Show | 41 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.104-1163A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773553 | ||||||
| chrX:2773556
|
A | G | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-1160A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773556 | ||||||
| chrX:2773566
|
A | AGAAGGAA others(281): Show |
1 | a0001c0001t0002g0155 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(290): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773566 | |||||
| chrX:2773566
|
A | C | 1 | a0001c0002t0044g0035 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.104-1150A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773566 | ||||||
| chrX:2773566
|
AGAAGGAA others(73): Show |
A | 6 | a0001c0001t0001g0070a0001c0001t0001g0114a0001c0001t0002g0197others(3): Show | 6 | HG01361.hp2 HG01934.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.104-1070_104-991de others(81): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773566 | |||||
| chrX:2773566
|
AGAAGGAA others(201): Show |
A | 2 | a0001c0001t0010g0193a0002c0003t0008g0066 | 2 | HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.104-1071_104-864de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773566 | |||||
| chrX:2773567
|
G | GAGGGAGA others(233): Show |
1 | a0001c0001t0003g0158 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.104-1148_104-1147i others(242): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773567 | |||||
| chrX:2773569
|
A | AGGAAGGA others(169): Show |
1 | a0001c0002t0005g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(178): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773569 | |||||
| chrX:2773569
|
A | AGGAAGGA others(57): Show |
1 | a0001c0001t0021g0278 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.104-1132_104-1131i others(66): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773569 | |||||
| chrX:2773569
|
A | G | 44 | a0001c0001t0001g0057a0001c0001t0001g0069a0001c0001t0001g0089others(41): Show | 44 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.104-1147A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773569 | ||||||
| chrX:2773572
|
A | G | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-1144A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773572 | ||||||
| chrX:2773573
|
A | G | 1 | a0001c0001t0003g0158 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.104-1143A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773573 | ||||||
| chrX:2773574
|
G | A | 1 | a0001c0001t0003g0158 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.104-1142G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773574 | ||||||
| chrX:2773577
|
A | G | 1 | a0001c0001t0003g0158 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.104-1139A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773577 | ||||||
| chrX:2773581
|
G | A | 1 | a0001c0001t0003g0158 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.104-1135G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773581 | ||||||
| chrX:2773582
|
A | AGAGGGAA others(1): Show |
2 | a0001c0001t0001g0316a0001c0001t0009g0246 | 2 | HG00642.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.104-1132_104-1131i others(10): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773582 | |||||
| chrX:2773582
|
A | C | 1 | a0001c0001t0001g0264 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.104-1134A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773582 | ||||||
| chrX:2773582
|
A | G | 1 | a0001c0001t0003g0158 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.104-1134A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773582 | ||||||
| chrX:2773582
|
AGAAG | A | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.104-1123_104-1120d others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773582 | |||||
| chrX:2773582
|
AGAAGGAA others(57): Show |
A | 9 | a0001c0001t0001g0237a0001c0001t0013g0303a0001c0001t0013g0307others(6): Show | 9 | HG01515.hp2 HG01517.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.104-1070_104-1007d others(66): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773582 | |||||
| chrX:2773582
|
AGAAGGAA others(169): Show |
A | 1 | a0001c0001t0011g0242 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.104-1118_104-943de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773582 | |||||
| chrX:2773582
|
AGAAGGAA others(185): Show |
A | 2 | a0001c0001t0016g0277a0001c0001t0024g0184 | 2 | HG03239.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.104-1070_104-879de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773582 | |||||
| chrX:2773585
|
A | AGGAAGGA others(169): Show |
1 | a0001c0001t0005g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(178): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773585 | |||||
| chrX:2773585
|
A | AGGAAGGA others(105): Show |
1 | a0001c0001t0003g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.104-1116_104-1115i others(114): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773585 | |||||
| chrX:2773585
|
A | AGGAAGGA others(473): Show |
1 | a0001c0001t0005g0145 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.104-1116_104-1115i others(482): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773585 | |||||
| chrX:2773585
|
A | G | 34 | a0001c0001t0001g0057a0001c0001t0001g0069a0001c0001t0001g0134others(31): Show | 34 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(31): Show |
intron_variant | MODIFIER | c.104-1131A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773585 | ||||||
| chrX:2773588
|
A | G | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-1128A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773588 | ||||||
| chrX:2773598
|
A | AGAAGGAA others(89): Show |
1 | a0001c0001t0001g0295 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(98): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773598 | |||||
| chrX:2773598
|
AGAAGGAA others(41): Show |
A | 14 | a0001c0001t0001g0157a0001c0001t0001g0264a0001c0001t0001g0290others(11): Show | 14 | HG00738.hp2 HG01257.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.104-1070_104-1023d others(50): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773598 | |||||
| chrX:2773598
|
AGAAGGAA others(153): Show |
A | 2 | a0001c0001t0001g0105a0001c0001t0002g0129 | 2 | HG00099.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.104-1102_104-943de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773598 | |||||
| chrX:2773598
|
AGAAGGAA others(169): Show |
A | 3 | a0001c0001t0001g0204a0001c0001t0007g0064a0001c0002t0041g0140 | 3 | HG01070.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.104-1070_104-895de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773598 | |||||
| chrX:2773600
|
A | AG | 1 | a0001c0001t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.104-1116_104-1115i others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773600 | ||||||
| chrX:2773601
|
A | AGGAAGGA others(137): Show |
1 | a0001c0005t0015g0045 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(146): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773601 | |||||
| chrX:2773601
|
A | AGGAAGGA others(217): Show |
1 | a0001c0001t0002g0274 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.104-1100_104-1099i others(226): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773601 | |||||
| chrX:2773601
|
A | G | 30 | a0001c0001t0001g0057a0001c0001t0001g0069a0001c0001t0001g0134others(27): Show | 30 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.104-1115A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773601 | ||||||
| chrX:2773604
|
A | G | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-1112A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773604 | ||||||
| chrX:2773614
|
A | AGAAGGAA others(41): Show |
1 | a0001c0001t0003g0215 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.104-1087_104-1086i others(50): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773614 | |||||
| chrX:2773614
|
A | C | 12 | a0001c0001t0001g0221a0001c0001t0001g0280a0001c0001t0003g0047others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.104-1102A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773614 | ||||||
| chrX:2773614
|
AGAAGGAA others(25): Show |
A | 8 | a0001c0001t0001g0090a0001c0001t0001g0104a0001c0001t0003g0039others(5): Show | 8 | HG00673.hp1 HG00741.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-1070_104-1039d others(34): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773614 | |||||
| chrX:2773614
|
AGAAGGAA others(137): Show |
A | 1 | a0001c0001t0047g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.104-1086_104-943de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773614 | |||||
| chrX:2773614
|
AGAAGGAA others(153): Show |
A | 5 | a0001c0001t0002g0072a0001c0001t0003g0063a0001c0001t0014g0096others(2): Show | 5 | HG02451.hp1 HG02698.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-1070_104-911de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773614 | |||||
| chrX:2773617
|
A | AGGAAGAA others(197): Show |
1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.104-1094_104-1093i others(206): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773617 | |||||
| chrX:2773617
|
A | AGGAAGGA others(89): Show |
1 | a0001c0001t0001g0316 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.104-1084_104-1083i others(98): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773617 | |||||
| chrX:2773617
|
A | AGGAAGGA others(185): Show |
1 | a0001c0001t0005g0284 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.104-1084_104-1083i others(194): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773617 | |||||
| chrX:2773617
|
A | G | 19 | a0001c0001t0001g0057a0001c0001t0001g0069a0001c0001t0001g0134others(16): Show | 19 | HG00280.hp1 HG00408.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.104-1099A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773617 | ||||||
| chrX:2773630
|
A | AGAAGGAA others(57): Show |
1 | a0001c0001t0004g0079 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(66): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773630 | |||||
| chrX:2773630
|
A | AGAAGGAA others(73): Show |
1 | a0001c0001t0001g0056 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773630 | |||||
| chrX:2773630
|
A | AGAAGGAA others(329): Show |
1 | a0001c0001t0020g0131 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.104-959_104-958ins others(336): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773630 | |||||
| chrX:2773630
|
A | C | 9 | a0001c0001t0001g0189a0001c0001t0001g0238a0001c0001t0003g0047others(6): Show | 9 | HG00438.hp1 HG01361.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.104-1086A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773630 | ||||||
| chrX:2773630
|
AGAAGGAA others(9): Show |
A | 29 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0069others(26): Show | 29 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.104-1070_104-1055d others(18): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773630 | |||||
| chrX:2773630
|
AGAAGGAA others(121): Show |
A | 8 | a0001c0001t0001g0221a0001c0001t0002g0291a0001c0001t0002g0299others(5): Show | 8 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-991_104-864del | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773630 | |||||
| chrX:2773630
|
AGAAGGAA others(137): Show |
A | 7 | a0001c0001t0001g0057a0001c0001t0001g0312a0001c0001t0002g0117others(4): Show | 7 | HG00280.hp1 HG00544.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.104-1070_104-927de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773630 | |||||
| chrX:2773633
|
A | AGGAAGGA others(233): Show |
1 | a0001c0001t0001g0164 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(242): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773633 | |||||
| chrX:2773633
|
A | AGGAAGGA others(73): Show |
1 | a0001c0001t0003g0250 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773633 | |||||
| chrX:2773633
|
A | AGGAAGGA others(9): Show |
2 | a0001c0001t0004g0222a0001c0001t0004g0245 | 2 | NA18952.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.104-1071_104-1070i others(18): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773633 | |||||
| chrX:2773633
|
A | AGGAAGGA others(25): Show |
1 | a0001c0001t0001g0023 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(34): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773633 | |||||
| chrX:2773633
|
A | AGGAAGGA others(73): Show |
1 | a0001c0001t0019g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773633 | |||||
| chrX:2773633
|
A | G | 14 | a0001c0001t0001g0134a0001c0001t0001g0142a0001c0001t0001g0214others(11): Show | 14 | HG00642.hp1 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.104-1083A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773633 | ||||||
| chrX:2773636
|
A | AAGGAAGG others(24): Show |
1 | a0001c0002t0034g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.104-1072_104-1071i others(33): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773636 | |||||
| chrX:2773644
|
AGCGAAGG others(186): Show |
A | 1 | a0001c0001t0013g0309 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.104-1071_104-879de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773644 | ||||||
| chrX:2773646
|
C | A | 165 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(162): Show | 165 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.104-1070C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773646 | ||||||
| chrX:2773646
|
C | CGAAGGAA others(9): Show |
1 | a0001c0001t0011g0208 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.104-974_104-959dup others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773646 | |||||
| chrX:2773646
|
C | CGAAGGAA others(89): Show |
1 | a0001c0002t0007g0276 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.104-1054_104-959du others(97): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773646 | |||||
| chrX:2773646
|
C | CGAAGGAA others(57): Show |
1 | a0001c0001t0006g0080 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.104-1055_104-1054i others(66): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773646 | |||||
| chrX:2773646
|
C | CGAAGGAA others(457): Show |
1 | a0002c0003t0007g0009 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.104-1055_104-1054i others(466): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773646 | |||||
| chrX:2773646
|
CGAAGGAA others(41): Show |
C | 2 | a0001c0001t0001g0087a0001c0001t0003g0297 | 2 | HG03239.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.104-1006_104-959de others(49): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773646 | |||||
| chrX:2773646
|
CGAAGGAA others(89): Show |
C | 1 | a0001c0001t0028g0130 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.104-1054_104-959de others(97): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773646 | |||||
| chrX:2773649
|
A | AGGAAGGA others(56): Show |
1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.104-1042_104-1041i others(65): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773649 | |||||
| chrX:2773649
|
A | AGGAAGGA others(153): Show |
1 | a0001c0001t0036g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.104-1004_104-1003i others(162): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773649 | |||||
| chrX:2773649
|
A | AGGAAGGA others(25): Show |
1 | a0001c0001t0004g0111 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.104-1036_104-1035i others(34): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773649 | |||||
| chrX:2773649
|
A | AGGAAGGA others(41): Show |
6 | a0001c0001t0001g0110a0001c0001t0001g0267a0001c0001t0001g0270others(3): Show | 6 | NA18747.hp2 NA18947.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.104-1036_104-1035i others(50): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773649 | |||||
| chrX:2773649
|
A | AGGAAGGA others(25): Show |
1 | a0001c0001t0028g0279 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.104-1052_104-1051i others(34): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773649 | |||||
| chrX:2773649
|
A | AGGAAGGA others(121): Show |
2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.104-1052_104-1051i others(130): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773649 | |||||
| chrX:2773649
|
A | G | 15 | a0001c0001t0001g0134a0001c0001t0001g0196a0001c0001t0001g0214others(12): Show | 15 | HG01168.hp1 HG02109.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.104-1067A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773649 | ||||||
| chrX:2773652
|
A | G | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-1064A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773652 | ||||||
| chrX:2773662
|
A | C | 8 | a0001c0001t0001g0216a0001c0001t0002g0097a0001c0001t0004g0318others(5): Show | 8 | HG00423.hp2 HG01261.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.104-1054A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773662 | ||||||
| chrX:2773662
|
AGAAGGAA others(105): Show |
A | 6 | a0001c0001t0001g0015a0001c0001t0001g0189a0001c0001t0001g0213others(3): Show | 6 | HG00438.hp1 HG03688.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.104-975_104-864del | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773662 | |||||
| chrX:2773665
|
A | AGGAAGGA others(57): Show |
1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.104-1004_104-1003i others(66): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773665 | |||||
| chrX:2773665
|
A | AGGAAGGA others(41): Show |
3 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0004g0126 | 3 | NA18961.hp1 NA18962.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.104-1020_104-1019i others(50): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773665 | |||||
| chrX:2773665
|
A | AGGAAGGA others(25): Show |
3 | a0001c0001t0001g0043a0001c0001t0001g0225a0001c0001t0001g0265 | 3 | HG00323.hp2 NA18950.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.104-1036_104-1035i others(34): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773665 | |||||
| chrX:2773665
|
A | AGGAAGGA others(105): Show |
1 | a0001c0001t0001g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.104-1036_104-1035i others(114): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773665 | |||||
| chrX:2773665
|
A | G | 16 | a0001c0001t0001g0134a0001c0001t0001g0143a0001c0001t0001g0144others(13): Show | 16 | HG00438.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.104-1051A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773665 | ||||||
| chrX:2773668
|
A | AAGGAAGG others(8): Show |
1 | a0001c0001t0005g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.104-1040_104-1039i others(17): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773668 | |||||
| chrX:2773668
|
A | G | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-1048A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773668 | ||||||
| chrX:2773670
|
GGAAGGAG others(8): Show |
G | 1 | a0001c0001t0001g0296 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.104-1044_104-1030d others(17): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773670 | |||||
| chrX:2773678
|
A | AGAAGGAA others(377): Show |
2 | a0002c0003t0040g0310a0002c0003t0045g0311 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.104-1007_104-1006i others(386): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773678 | |||||
| chrX:2773678
|
A | C | 7 | a0001c0001t0001g0115a0001c0001t0001g0216a0001c0001t0001g0244others(4): Show | 7 | HG00423.hp2 HG00733.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.104-1038A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773678 | ||||||
| chrX:2773678
|
AGAAGGAA others(89): Show |
A | 6 | a0001c0001t0001g0214a0001c0001t0001g0249a0001c0001t0001g0304others(3): Show | 6 | HG02258.hp2 HG02683.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.104-959_104-864del others(96): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773678 | |||||
| chrX:2773681
|
A | G | 11 | a0001c0001t0001g0134a0001c0001t0001g0143a0001c0001t0001g0144others(8): Show | 11 | HG02109.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.104-1035A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773681 | ||||||
| chrX:2773692
|
AGAGAAGG others(138): Show |
A | 1 | a0001c0001t0002g0314 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.104-1023_104-879de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773692 | ||||||
| chrX:2773694
|
A | AGAAGGAA others(265): Show |
1 | a0002c0003t0008g0125 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.104-975_104-974ins others(272): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773694 | |||||
| chrX:2773694
|
A | AGAAGGAA others(277): Show |
1 | a0001c0001t0027g0026 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.104-1004_104-1003i others(286): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773694 | |||||
| chrX:2773694
|
A | AGAAGGAA others(9): Show |
1 | a0001c0001t0002g0156 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.104-1007_104-1006i others(18): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773694 | |||||
| chrX:2773694
|
A | C | 1 | a0001c0001t0001g0216 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.104-1022A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773694 | ||||||
| chrX:2773694
|
AGAAGGAA others(73): Show |
A | 1 | a0001c0002t0012g0049 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.104-958_104-879del others(80): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773694 | |||||
| chrX:2773697
|
A | AGGAAGGA others(265): Show |
1 | a0002c0008t0037g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.104-988_104-987ins others(272): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773697 | |||||
| chrX:2773697
|
A | AGGAAGGA others(153): Show |
1 | a0001c0001t0003g0236 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.104-991_104-990ins others(160): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773697 | |||||
| chrX:2773697
|
A | AGGAAGGA others(249): Show |
1 | a0001c0001t0005g0020 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.104-1004_104-1003i others(258): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773697 | |||||
| chrX:2773697
|
A | G | 9 | a0001c0001t0001g0134a0001c0001t0003g0061a0001c0001t0003g0283others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.104-1019A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773697 | ||||||
| chrX:2773708
|
AGAGAAGG others(122): Show |
A | 1 | a0001c0001t0021g0021 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.104-1007_104-879de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773708 | ||||||
| chrX:2773710
|
A | AGAAGGAA others(41): Show |
1 | a0002c0003t0031g0109 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.104-975_104-974ins others(48): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773710 | |||||
| chrX:2773710
|
A | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0183a0001c0001t0001g0205 | 3 | HG00323.hp1 HG02273.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.104-1006A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773710 | ||||||
| chrX:2773710
|
AGAAGGAA others(57): Show |
A | 6 | a0001c0001t0001g0037a0001c0001t0009g0031a0001c0001t0016g0233others(3): Show | 6 | HG02451.hp2 HG02976.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-958_104-895del others(64): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773710 | |||||
| chrX:2773713
|
A | AGGAAGGA others(281): Show |
1 | a0001c0001t0005g0003 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.104-988_104-987ins others(288): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773713 | |||||
| chrX:2773713
|
A | AGGAAGGA others(281): Show |
2 | a0001c0001t0023g0005a0001c0001t0023g0006 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.104-988_104-987ins others(288): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773713 | |||||
| chrX:2773713
|
A | G | 12 | a0001c0001t0001g0134a0001c0001t0001g0143a0001c0001t0001g0144others(9): Show | 12 | HG02109.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.104-1003A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773713 | ||||||
| chrX:2773718
|
G | GGAAGGAG others(316): Show |
1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-988_104-987ins others(323): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773718 | |||||
| chrX:2773722
|
G | GGAGAGAA others(175): Show |
1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-980_104-979ins others(182): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773722 | |||||
| chrX:2773726
|
A | AGAAGGAA others(9): Show |
1 | a0001c0001t0012g0203 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.104-975_104-974ins others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773726 | |||||
| chrX:2773726
|
A | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0104a0001c0001t0001g0183others(1): Show | 4 | HG02273.hp1 HG02630.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-990A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773726 | ||||||
| chrX:2773726
|
AGAAGGAA others(25): Show |
A | 1 | a0001c0001t0001g0244 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.104-974_104-943del others(32): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773726 | |||||
| chrX:2773726
|
AGAAGGAA others(41): Show |
A | 8 | a0001c0001t0001g0038a0001c0001t0001g0089a0001c0001t0001g0118others(5): Show | 8 | HG02071.hp1 HG02165.hp2 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-958_104-911del others(48): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773726 | |||||
| chrX:2773729
|
A | AGGAAGGA others(281): Show |
1 | a0001c0002t0007g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.104-972_104-971ins others(288): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773729 | |||||
| chrX:2773729
|
A | G | 13 | a0001c0001t0001g0134a0001c0001t0001g0143a0001c0001t0001g0144others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.104-987A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773729 | ||||||
| chrX:2773742
|
A | AGAAGGAA others(245): Show |
1 | a0001c0002t0044g0035 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.104-966_104-965ins others(252): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773742 | |||||
| chrX:2773742
|
A | AGAAGGAA others(9): Show |
5 | a0001c0001t0001g0056a0001c0001t0003g0215a0001c0001t0004g0079others(2): Show | 5 | HG02074.hp1 HG02129.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-942_104-927dup others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773742 | |||||
| chrX:2773742
|
A | C | 25 | a0001c0001t0001g0070a0001c0001t0001g0114a0001c0001t0001g0157others(22): Show | 25 | HG00408.hp2 HG00733.hp2 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.104-974A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773742 | ||||||
| chrX:2773742
|
AGAAGGAA others(9): Show |
A | 1 | a0001c0001t0001g0273 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.104-942_104-927del others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773742 | |||||
| chrX:2773742
|
AGAAGGAA others(25): Show |
A | 1 | a0001c0001t0003g0147 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.104-958_104-927del others(32): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773742 | |||||
| chrX:2773744
|
A | G | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-972A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773744 | ||||||
| chrX:2773745
|
A | AGGAAGGA others(361): Show |
1 | a0001c0001t0022g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.104-959_104-958ins others(368): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773745 | |||||
| chrX:2773745
|
A | G | 12 | a0001c0001t0001g0054a0001c0001t0001g0134a0001c0001t0001g0143others(9): Show | 12 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.104-971A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773745 | ||||||
| chrX:2773745
|
AG | A | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.104-969delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773745 | |||||
| chrX:2773752
|
A | AAGCTAG | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-962_104-961ins others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773752 | |||||
| chrX:2773756
|
A | AAG | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-960_104-959ins others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773756 | ||||||
| chrX:2773757
|
G | GAGAA | 1 | a0001c0001t0027g0026 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.104-959_104-958ins others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773757 | ||||||
| chrX:2773758
|
C | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0032others(111): Show | 115 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.104-958C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773758 | ||||||
| chrX:2773758
|
C | CGAAGGAA others(9): Show |
3 | a0001c0001t0005g0288a0001c0002t0007g0276a0004c0009t0035g0282 | 3 | HG01891.hp1 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.104-943_104-942ins others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773758 | |||||
| chrX:2773758
|
C | CGAAGGAA others(57): Show |
1 | a0001c0001t0005g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.104-943_104-942ins others(64): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773758 | |||||
| chrX:2773758
|
C | CGAAGGAA others(441): Show |
1 | a0001c0001t0025g0027 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.104-943_104-942ins others(448): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773758 | |||||
| chrX:2773758
|
C | CGAAGGAA others(25): Show |
1 | a0001c0001t0002g0097 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.104-942_104-911dup others(32): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773758 | |||||
| chrX:2773758
|
C | G | 1 | a0001c0001t0027g0026 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.104-958C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773758 | ||||||
| chrX:2773761
|
A | G | 9 | a0001c0001t0001g0054a0001c0001t0001g0134a0001c0001t0001g0143others(6): Show | 9 | HG02109.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.104-955A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773761 | ||||||
| chrX:2773773
|
G | T | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-943G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773773 | ||||||
| chrX:2773774
|
C | A | 61 | a0001c0001t0001g0018a0001c0001t0001g0054a0001c0001t0001g0069others(58): Show | 61 | HG00408.hp1 HG00609.hp1 HG01123.hp1 others(58): Show |
intron_variant | MODIFIER | c.104-942C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773774 | ||||||
| chrX:2773774
|
C | CGAAGGAA others(9): Show |
2 | a0001c0001t0001g0019a0001c0001t0005g0284 | 2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.104-879_104-864dup others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773774 | |||||
| chrX:2773774
|
C | CGAAGGAA others(281): Show |
1 | a0001c0001t0001g0074 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.104-927_104-926ins others(288): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773774 | |||||
| chrX:2773774
|
CGAAGGAA others(9): Show |
C | 4 | a0001c0001t0001g0216a0001c0001t0001g0225a0001c0001t0003g0250others(1): Show | 4 | HG00323.hp2 HG00423.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-879_104-864del others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773774 | |||||
| chrX:2773777
|
A | AGGAAGGA others(457): Show |
1 | a0001c0002t0007g0190 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.104-864_104-863ins others(464): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773777 | |||||
| chrX:2773777
|
A | AGGAAGGA others(9): Show |
1 | a0001c0001t0003g0012 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.104-924_104-923ins others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773777 | |||||
| chrX:2773777
|
A | G | 17 | a0001c0001t0001g0054a0001c0001t0001g0093a0001c0001t0001g0134others(14): Show | 17 | HG02080.hp1 HG02109.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.104-939A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773777 | ||||||
| chrX:2773786
|
G | GA | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-930_104-929ins others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773786 | ||||||
| chrX:2773790
|
A | AGAAGGAA others(617): Show |
1 | a0001c0002t0008g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.104-864_104-863ins others(624): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773790 | |||||
| chrX:2773790
|
A | C | 12 | a0001c0001t0001g0015a0001c0001t0001g0196a0001c0001t0001g0204others(9): Show | 12 | HG00673.hp1 HG01070.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.104-926A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773790 | ||||||
| chrX:2773793
|
A | AGGAAGGA others(105): Show |
1 | a0001c0001t0036g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.104-908_104-907ins others(112): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773793 | |||||
| chrX:2773793
|
A | G | 10 | a0001c0001t0001g0089a0001c0001t0001g0134a0001c0001t0005g0145others(7): Show | 10 | HG02109.hp2 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.104-923A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773793 | ||||||
| chrX:2773796
|
AAG | A | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-919_104-918del others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773796 | ||||||
| chrX:2773804
|
AG | A | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-911delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773804 | ||||||
| chrX:2773809
|
A | G | 8 | a0001c0001t0002g0108a0001c0001t0007g0064a0001c0001t0010g0193others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-907A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773809 | ||||||
| chrX:2773809
|
AG | A | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-905delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773809 | |||||
| chrX:2773823
|
G | A | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-893G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773823 | ||||||
| chrX:2773824
|
A | G | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-892A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773824 | ||||||
| chrX:2773825
|
A | G | 1 | a0001c0001t0017g0269 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.104-891A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773825 | ||||||
| chrX:2773826
|
G | GAA | 1 | a0001c0001t0001g0229 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.104-890_104-889ins others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773826 | ||||||
| chrX:2773828
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.104-888A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773828 | ||||||
| chrX:2773830
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.104-886G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773830 | ||||||
| chrX:2773832
|
A | AG | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-884_104-883ins others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773832 | ||||||
| chrX:2773835
|
GAGAGAAG others(10): Show |
G | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.104-877_104-861del others(17): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773835 | |||||
| chrX:2773836
|
AG | A | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.104-879delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773836 | ||||||
| chrX:2773839
|
G | T | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-877G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773839 | ||||||
| chrX:2773841
|
A | G | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-875A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773841 | ||||||
| chrX:2773842
|
G | GA | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-874_104-873ins others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773842 | ||||||
| chrX:2773844
|
A | G | 1 | a0001c0001t0002g0314 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.104-872A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773844 | ||||||
| chrX:2773844
|
A | T | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-872A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773844 | ||||||
| chrX:2773847
|
G | A | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-869G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773847 | ||||||
| chrX:2773849
|
A | G | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-867A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773849 | ||||||
| chrX:2773850
|
G | A | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-866G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773850 | ||||||
| chrX:2773857
|
G | T | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-859G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773857 | ||||||
| chrX:2773859
|
GAGGGC | G | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-853_104-849del others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773859 | |||||
| chrX:2773865
|
A | T | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-851A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773865 | ||||||
| chrX:2773871
|
G | A | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-845G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773871 | ||||||
| chrX:2773872
|
G | T | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-844G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773872 | ||||||
| chrX:2773873
|
A | G | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-843A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773873 | ||||||
| chrX:2773882
|
T | TG | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-832dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773882 | |||||
| chrX:2773885
|
C | A | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-831C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773885 | ||||||
| chrX:2773894
|
GA | G | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-818delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773894 | |||||
| chrX:2773896
|
A | G | 11 | a0001c0001t0007g0064a0001c0001t0010g0193a0001c0001t0020g0138others(8): Show | 11 | HG01243.hp2 HG02109.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.104-820A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773896 | ||||||
| chrX:2773910
|
AC | A | 1 | a0001c0001t0004g0243 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-804delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773910 | |||||
| chrX:2773932
|
A | T | 1 | a0001c0001t0011g0208 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.104-784A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773932 | ||||||
| chrX:2773946
|
GC | G | 1 | a0001c0001t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.104-766delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773946 | |||||
| chrX:2774018
|
A | ACC | 14 | a0001c0001t0001g0057a0001c0001t0001g0093a0001c0001t0001g0214others(11): Show | 14 | HG00280.hp1 HG00741.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.104-696_104-695dup others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2774018 | |||||
| chrX:2774021
|
C | CCT | 5 | a0001c0001t0001g0134a0001c0001t0003g0283a0001c0001t0020g0138others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.104-695_104-694ins others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774021 | ||||||
| chrX:2774084
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.104-632C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774084 | ||||||
| chrX:2774224
|
A | AC | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.104-489dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2774224 | |||||
| chrX:2774330
|
G | GAAAGAAA others(329): Show |
1 | a0001c0002t0005g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.104-372_104-371ins others(336): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2774330 | |||||
| chrX:2774330
|
G | GAAAGAAA others(326): Show |
1 | a0002c0003t0031g0109 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.104-372_104-371ins others(333): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2774330 | |||||
| chrX:2774330
|
G | GAAAGAAA others(324): Show |
6 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0020g0131others(3): Show | 6 | HG02572.hp2 HG02723.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-372_104-371ins others(331): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2774330 | |||||
| chrX:2774330
|
G | GAAAGAAA others(325): Show |
2 | a0001c0002t0034g0010a0002c0003t0007g0009 | 2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.104-372_104-371ins others(332): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2774330 | |||||
| chrX:2774330
|
G | GAAAGAAA others(338): Show |
3 | a0001c0001t0001g0134a0001c0001t0020g0138a0001c0002t0005g0034 | 3 | HG02109.hp2 HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.104-372_104-371ins others(345): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2774330 | |||||
| chrX:2774330
|
G | GAAAGAAA others(341): Show |
1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-372_104-371ins others(348): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2774330 | |||||
| chrX:2774355
|
T | C | 1 | a0001c0001t0013g0309 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.104-361T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774355 | ||||||
| chrX:2774399
|
CT | C | 5 | a0001c0001t0003g0063a0001c0001t0005g0003a0001c0001t0005g0020others(2): Show | 5 | HG01261.hp1 HG02630.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.104-316delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774399 | ||||||
| chrX:2774416
|
G | A | 1 | a0001c0001t0003g0033 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.104-300G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774416 | ||||||
| chrX:2774420
|
A | G | 117 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0041others(114): Show | 117 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.104-296A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774420 | ||||||
| chrX:2774422
|
C | CCCTGTG | 170 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0023others(167): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.104-293_104-288dup others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2774422 | |||||
| chrX:2774439
|
G | A | 1 | a0001c0002t0007g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.104-277G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774439 | ||||||
| chrX:2774446
|
T | TG | 1 | a0001c0001t0001g0115 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104-268dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2774446 | |||||
| chrX:2774556
|
T | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0023others(172): Show | 176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.104-160T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774556 | ||||||
| chrX:2774669
|
A | G | 94 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0041others(91): Show | 94 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.104-47A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774669 | ||||||
| chrX:2774703
|
T | C | 2 | a0001c0001t0001g0134a0001c0002t0005g0034 | 2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.104-13T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774703 | ||||||
| chrX:2774757
|
TG | T | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.127+21delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2774757 | |||||
| chrX:2774958
|
C | G | 1 | a0001c0001t0046g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127+219C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2774958 | ||||||
| chrX:2774959
|
TA | T | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.127+224delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2774959 | |||||
| chrX:2775026
|
G | C | 14 | a0001c0001t0001g0287a0001c0001t0003g0047a0001c0001t0003g0048others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.127+287G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775026 | ||||||
| chrX:2775070
|
T | C | 6 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0025g0317others(3): Show | 6 | HG00741.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+331T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775070 | ||||||
| chrX:2775071
|
C | G | 4 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0002t0007g0052others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+332C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775071 | ||||||
| chrX:2775075
|
C | A | 6 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0025g0317others(3): Show | 6 | HG00741.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+336C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775075 | ||||||
| chrX:2775120
|
C | G | 2 | a0001c0001t0003g0063a0001c0002t0005g0275 | 2 | HG02698.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.127+381C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775120 | ||||||
| chrX:2775124
|
G | T | 1 | a0001c0002t0007g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.127+385G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775124 | ||||||
| chrX:2775134
|
A | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0023others(172): Show | 176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.127+395A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775134 | ||||||
| chrX:2775332
|
GGTT | G | 1 | a0001c0001t0001g0296 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.127+595_127+597del others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2775332 | |||||
| chrX:2775517
|
TG | T | 1 | a0001c0001t0001g0032 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.127+783delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2775517 | |||||
| chrX:2775583
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0023others(166): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.127+844G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775583 | ||||||
| chrX:2775601
|
CT | C | 1 | a0001c0001t0025g0317 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.127+866delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2775601 | |||||
| chrX:2775618
|
A | C | 16 | a0001c0001t0001g0093a0001c0001t0003g0137a0001c0001t0005g0145others(13): Show | 16 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.127+879A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775618 | ||||||
| chrX:2775664
|
G | C | 1 | a0001c0001t0013g0309 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.127+925G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775664 | ||||||
| chrX:2775717
|
A | AG | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.127+980dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2775717 | |||||
| chrX:2775783
|
T | C | 273 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.127+1044T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775783 | ||||||
| chrX:2775863
|
A | G | 3 | a0001c0001t0001g0287a0001c0001t0013g0309a0001c0001t0025g0317 | 3 | HG01884.hp1 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.127+1124A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775863 | ||||||
| chrX:2775866
|
G | A | 1 | a0001c0001t0013g0309 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.127+1127G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775866 | ||||||
| chrX:2775955
|
C | CA | 1 | a0001c0001t0002g0180 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.127+1233dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2775955 | |||||
| chrX:2775955
|
CA | C | 2 | a0001c0001t0002g0194a0001c0001t0003g0033 | 2 | NA18982.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.127+1233delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2775955 | |||||
| chrX:2775955
|
CAAA | C | 1 | a0001c0001t0001g0057 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.127+1231_127+1233d others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2775955 | |||||
| chrX:2775965
|
AAAAAAAA others(1): Show |
A | 1 | a0001c0001t0025g0317 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.127+1231_127+1238d others(10): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2775965 | |||||
| chrX:2775966
|
AAAAAAAG | A | 11 | a0001c0001t0001g0115a0001c0001t0001g0157a0001c0001t0001g0186others(8): Show | 11 | HG01517.hp1 HG01884.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.127+1232_127+1238d others(9): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2775966 | |||||
| chrX:2775967
|
AAAAAAG | A | 237 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(234): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.127+1233_127+1238d others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2775967 | |||||
| chrX:2775968
|
AAAAAG | A | 28 | a0001c0001t0001g0041a0001c0001t0001g0093a0001c0001t0002g0257others(25): Show | 28 | HG01070.hp2 HG01071.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.127+1249_127+1253d others(7): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2775968 | |||||
| chrX:2775969
|
AAAAG | A | 1 | a0001c0001t0005g0284 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127+1234_127+1237d others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2775969 | |||||
| chrX:2775970
|
AAAG | A | 4 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0002t0007g0052others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+1234_127+1236d others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2775970 | |||||
| chrX:2775972
|
AG | A | 3 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0225 | 3 | HG00323.hp2 NA18962.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.127+1234delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775972 | ||||||
| chrX:2776014
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.127+1275G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776014 | ||||||
| chrX:2776028
|
G | GC | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.127+1291dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2776028 | |||||
| chrX:2776100
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.127+1361T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776100 | ||||||
| chrX:2776137
|
G | GCCACA | 169 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.127+1399_127+1400i others(7): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2776137 | |||||
| chrX:2776160
|
T | G | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.127+1421T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776160 | ||||||
| chrX:2776163
|
A | C | 24 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0093others(21): Show | 24 | HG01074.hp1 HG01884.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.127+1424A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776163 | ||||||
| chrX:2776171
|
G | C | 1 | a0002c0008t0037g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.127+1432G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776171 | ||||||
| chrX:2776172
|
C | CG | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.127+1434dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2776172 | |||||
| chrX:2776199
|
G | T | 278 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(275): Show | 279 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.127+1460G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776199 | ||||||
| chrX:2776208
|
T | C | 1 | a0001c0001t0002g0132 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.127+1469T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776208 | ||||||
| chrX:2776211
|
T | C | 6 | a0001c0001t0001g0304a0001c0001t0002g0132a0001c0001t0005g0305others(3): Show | 6 | HG01243.hp2 HG02258.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+1472T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776211 | ||||||
| chrX:2776262
|
T | G | 7 | a0001c0001t0001g0134a0001c0001t0001g0260a0001c0001t0003g0283others(4): Show | 7 | HG01884.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+1523T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776262 | ||||||
| chrX:2776321
|
A | G | 1 | a0001c0002t0005g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.127+1582A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776321 | ||||||
| chrX:2776328
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.127+1589C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776328 | ||||||
| chrX:2776357
|
G | C | 7 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0020g0131others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.127+1618G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776357 | ||||||
| chrX:2776370
|
T | C | 2 | a0001c0001t0001g0287a0001c0001t0027g0026 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.127+1631T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776370 | ||||||
| chrX:2776370
|
TACAAGGT others(1): Show |
T | 4 | a0001c0001t0002g0129a0001c0001t0003g0219a0002c0003t0040g0310others(1): Show | 4 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+1633_127+1640d others(10): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2776370 | |||||
| chrX:2776388
|
G | A | 132 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(129): Show | 132 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.127+1649G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776388 | ||||||
| chrX:2776420
|
CG | C | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.127+1684delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2776420 | |||||
| chrX:2776446
|
A | C | 7 | a0003c0004t0001g0226a0003c0004t0001g0227a0003c0004t0002g0058others(4): Show | 7 | HG00099.hp1 HG00140.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.127+1707A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776446 | ||||||
| chrX:2776472
|
T | TG | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.127+1735dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2776472 | |||||
| chrX:2776492
|
C | T | 11 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0007g0064others(8): Show | 11 | HG02257.hp2 HG02451.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.127+1753C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776492 | ||||||
| chrX:2776516
|
A | AG | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.127+1781dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2776516 | |||||
| chrX:2776553
|
T | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(206): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.127+1814T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776553 | ||||||
| chrX:2776564
|
G | C | 1 | a0001c0007t0032g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.127+1825G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776564 | ||||||
| chrX:2776608
|
A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(264): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.127+1869A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776608 | ||||||
| chrX:2776609
|
AG | A | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.127+1872delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2776609 | |||||
| chrX:2776649
|
GT | G | 1 | a0001c0001t0001g0296 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.127+1912delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2776649 | |||||
| chrX:2776681
|
T | TA | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.127+1948dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2776681 | |||||
| chrX:2776690
|
C | CA | 2 | a0001c0001t0003g0082a0001c0001t0003g0215 | 2 | NA18941.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.127+1959dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2776690 | |||||
| chrX:2776709
|
A | G | 8 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0005g0030others(5): Show | 8 | HG02559.hp1 HG02886.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.127+1970A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776709 | ||||||
| chrX:2776716
|
C | T | 11 | a0001c0001t0001g0315a0001c0001t0003g0047a0001c0001t0003g0048others(8): Show | 11 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.127+1977C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776716 | ||||||
| chrX:2776739
|
T | C | 6 | a0001c0001t0001g0169a0001c0001t0001g0229a0001c0001t0003g0100others(3): Show | 6 | HG00408.hp1 NA18940.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+2000T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776739 | ||||||
| chrX:2776765
|
G | A | 67 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0083others(64): Show | 67 | HG00544.hp2 HG00741.hp1 HG01070.hp2 others(64): Show |
intron_variant | MODIFIER | c.127+2026G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776765 | ||||||
| chrX:2776772
|
C | T | 48 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0093others(45): Show | 48 | HG00544.hp2 HG00741.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.127+2033C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776772 | ||||||
| chrX:2776780
|
G | A | 23 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0003g0137others(20): Show | 23 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(20): Show |
intron_variant | MODIFIER | c.127+2041G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776780 | ||||||
| chrX:2776796
|
C | A | 16 | a0001c0001t0003g0283a0001c0001t0005g0029a0001c0001t0005g0030others(13): Show | 16 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.127+2057C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776796 | ||||||
| chrX:2776845
|
TCAA | T | 33 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0093others(30): Show | 33 | HG00741.hp1 HG01074.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.127+2122_127+2124d others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2776845 | |||||
| chrX:2776861
|
CA | C | 1 | a0001c0001t0004g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.127+2127delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2776861 | |||||
| chrX:2776990
|
C | T | 1 | a0001c0001t0027g0026 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.127+2251C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776990 | ||||||
| chrX:2777065
|
TC | T | 1 | a0001c0001t0001g0115 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.127+2328delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2777065 | |||||
| chrX:2777133
|
G | A | 1 | a0001c0001t0027g0026 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.127+2394G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777133 | ||||||
| chrX:2777150
|
C | A | 5 | a0001c0001t0022g0004a0001c0001t0023g0005a0001c0001t0023g0006others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+2411C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777150 | ||||||
| chrX:2777174
|
A | T | 8 | a0002c0008t0037g0098a0003c0004t0001g0226a0003c0004t0001g0227others(5): Show | 8 | HG00099.hp1 HG00140.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.127+2435A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777174 | ||||||
| chrX:2777243
|
G | T | 5 | a0001c0001t0022g0004a0001c0001t0023g0005a0001c0001t0023g0006others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+2504G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777243 | ||||||
| chrX:2777299
|
A | G | 9 | a0001c0001t0001g0315a0001c0001t0003g0047a0001c0001t0003g0048others(6): Show | 9 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.127+2560A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777299 | ||||||
| chrX:2777315
|
AT | A | 1 | a0001c0001t0001g0296 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.127+2580delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2777315 | |||||
| chrX:2777332
|
TC | T | 1 | a0001c0001t0001g0115 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.127+2595delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2777332 | |||||
| chrX:2777410
|
CA | C | 5 | a0001c0001t0022g0004a0001c0001t0023g0005a0001c0001t0023g0006others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+2679delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2777410 | |||||
| chrX:2777449
|
CA | C | 1 | a0004c0009t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.127+2712delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2777449 | |||||
| chrX:2777456
|
TGTG | T | 1 | a0001c0001t0001g0225 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.127+2721_127+2723d others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2777456 | |||||
| chrX:2777459
|
G | C | 1 | a0001c0001t0001g0251 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.127+2720G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777459 | ||||||
| chrX:2777598
|
T | TA | 5 | a0001c0001t0022g0004a0001c0001t0023g0005a0001c0001t0023g0006others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+2868dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2777598 | |||||
| chrX:2777598
|
TA | T | 1 | a0001c0001t0001g0115 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.127+2868delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2777598 | |||||
| chrX:2777759
|
G | A | 1 | a0001c0001t0002g0274 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.127+3020G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777759 | ||||||
| chrX:2777789
|
A | G | 43 | a0001c0001t0001g0093a0001c0001t0001g0315a0001c0001t0002g0314others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.127+3050A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777789 | ||||||
| chrX:2777819
|
A | G | 43 | a0001c0001t0001g0093a0001c0001t0001g0315a0001c0001t0002g0314others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.127+3080A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777819 | ||||||
| chrX:2777823
|
A | G | 17 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0284others(14): Show | 17 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.127+3084A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777823 | ||||||
| chrX:2777831
|
C | CG | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.127+3095dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2777831 | |||||
| chrX:2777857
|
G | A | 5 | a0001c0001t0001g0212a0001c0001t0001g0232a0001c0001t0001g0234others(2): Show | 5 | HG01175.hp1 HG03491.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+3118G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777857 | ||||||
| chrX:2777978
|
G | GA | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.127+3247dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2777978 | |||||
| chrX:2777990
|
G | T | 1 | a0001c0001t0009g0246 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.127+3251G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777990 | ||||||
| chrX:2778304
|
A | C | 1 | a0002c0003t0001g0028 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.127+3565A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778304 | ||||||
| chrX:2778358
|
C | T | 4 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0284others(1): Show | 4 | HG02280.hp2 HG02559.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+3619C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778358 | ||||||
| chrX:2778389
|
A | T | 3 | a0001c0001t0005g0030a0001c0001t0005g0284a0001c0002t0005g0285 | 3 | HG02559.hp1 HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.127+3650A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778389 | ||||||
| chrX:2778511
|
C | T | 1 | a0001c0002t0005g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.128-3555C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778511 | ||||||
| chrX:2778519
|
G | A | 42 | a0001c0001t0001g0093a0001c0001t0001g0315a0001c0001t0002g0314others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.128-3547G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778519 | ||||||
| chrX:2778625
|
G | T | 8 | a0001c0001t0007g0064a0001c0001t0010g0193a0001c0001t0022g0004others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.128-3441G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778625 | ||||||
| chrX:2778758
|
C | G | 1 | a0001c0001t0001g0251 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.128-3308C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778758 | ||||||
| chrX:2778774
|
A | AT | 1 | a0001c0001t0036g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.128-3292_128-3291i others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778774 | ||||||
| chrX:2778775
|
C | CT | 6 | a0001c0001t0001g0093a0001c0001t0001g0103a0001c0001t0002g0072others(3): Show | 6 | HG03516.hp1 NA18939.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-3275dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2778775 | |||||
| chrX:2778775
|
C | T | 8 | a0001c0001t0007g0064a0001c0001t0010g0193a0001c0001t0022g0004others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.128-3291C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778775 | ||||||
| chrX:2778775
|
CT | C | 24 | a0001c0001t0001g0032a0001c0001t0001g0315a0001c0001t0003g0047others(21): Show | 24 | HG00099.hp1 HG00140.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.128-3275delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2778775 | |||||
| chrX:2778775
|
CTT | C | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.128-3276_128-3275d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2778775 | |||||
| chrX:2778804
|
C | T | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.128-3262C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778804 | ||||||
| chrX:2778805
|
G | A | 24 | a0001c0001t0001g0093a0001c0001t0001g0315a0001c0001t0002g0314others(21): Show | 24 | HG01074.hp1 HG01109.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.128-3261G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778805 | ||||||
| chrX:2778851
|
G | A | 29 | a0001c0001t0001g0093a0001c0001t0001g0315a0001c0001t0002g0314others(26): Show | 29 | HG00741.hp1 HG01074.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.128-3215G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778851 | ||||||
| chrX:2778852
|
C | T | 29 | a0001c0001t0001g0093a0001c0001t0001g0315a0001c0001t0002g0314others(26): Show | 29 | HG00741.hp1 HG01074.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.128-3214C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778852 | ||||||
| chrX:2778866
|
C | T | 6 | a0001c0001t0001g0296a0001c0001t0022g0004a0001c0001t0023g0005others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-3200C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778866 | ||||||
| chrX:2778952
|
C | CG | 1 | a0001c0001t0005g0113 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.128-3110dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2778952 | |||||
| chrX:2779038
|
A | G | 1 | a0001c0001t0003g0148 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.128-3028A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779038 | ||||||
| chrX:2779060
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.128-3006A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779060 | ||||||
| chrX:2779113
|
A | C | 22 | a0001c0001t0001g0093a0001c0001t0001g0304a0001c0001t0002g0314others(19): Show | 22 | HG01074.hp1 HG01109.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.128-2953A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779113 | ||||||
| chrX:2779122
|
CT | C | 4 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0004g0111others(1): Show | 4 | HG01074.hp1 HG01099.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-2934delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2779122 | |||||
| chrX:2779169
|
A | C | 1 | a0001c0001t0002g0274 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.128-2897A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779169 | ||||||
| chrX:2779232
|
A | AG | 1 | a0001c0001t0003g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.128-2832dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2779232 | |||||
| chrX:2779238
|
AG | A | 1 | a0001c0001t0003g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.128-2826delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2779238 | |||||
| chrX:2779262
|
A | AC | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.128-2804_128-2803i others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779262 | ||||||
| chrX:2779277
|
A | G | 27 | a0001c0001t0001g0287a0001c0001t0001g0315a0001c0001t0003g0047others(24): Show | 27 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.128-2789A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779277 | ||||||
| chrX:2779312
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.128-2754G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779312 | ||||||
| chrX:2779330
|
T | TA | 5 | a0001c0001t0001g0221a0001c0001t0001g0270a0001c0001t0003g0120others(2): Show | 5 | HG03927.hp2 NA19054.hp1 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-2718dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2779330 | |||||
| chrX:2779330
|
TA | T | 27 | a0001c0001t0001g0032a0001c0001t0001g0054a0001c0001t0001g0083others(24): Show | 27 | HG00099.hp1 HG00140.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.128-2718delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2779330 | |||||
| chrX:2779330
|
TAA | T | 22 | a0001c0001t0001g0093a0001c0001t0002g0314a0001c0001t0003g0061others(19): Show | 22 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.128-2719_128-2718d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2779330 | |||||
| chrX:2779330
|
TAAA | T | 15 | a0001c0001t0001g0315a0001c0001t0003g0047a0001c0001t0003g0048others(12): Show | 15 | HG00741.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.128-2720_128-2718d others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2779330 | |||||
| chrX:2779330
|
TAAAA | T | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.128-2721_128-2718d others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2779330 | |||||
| chrX:2779333
|
A | T | 1 | a0001c0001t0006g0017 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.128-2733A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779333 | ||||||
| chrX:2779365
|
TG | T | 1 | a0001c0001t0003g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.128-2698delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2779365 | |||||
| chrX:2779388
|
AAAT | A | 2 | a0001c0001t0005g0030a0001c0001t0005g0284 | 2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.128-2659_128-2657d others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2779388 | |||||
| chrX:2779450
|
G | T | 1 | a0001c0001t0001g0229 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.128-2616G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779450 | ||||||
| chrX:2779550
|
G | A | 1 | a0001c0002t0044g0035 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.128-2516G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779550 | ||||||
| chrX:2779557
|
TC | T | 1 | a0001c0001t0001g0229 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.128-2505delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2779557 | |||||
| chrX:2779558
|
C | A | 1 | a0001c0001t0006g0017 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.128-2508C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779558 | ||||||
| chrX:2779650
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.128-2416T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779650 | ||||||
| chrX:2779669
|
C | G | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.128-2397C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779669 | ||||||
| chrX:2779739
|
C | T | 5 | a0001c0001t0001g0212a0001c0001t0001g0232a0001c0001t0001g0234others(2): Show | 5 | HG01175.hp1 HG03491.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-2327C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779739 | ||||||
| chrX:2779796
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.128-2270G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779796 | ||||||
| chrX:2779804
|
C | T | 25 | a0001c0001t0001g0093a0001c0001t0001g0287a0001c0001t0001g0315others(22): Show | 25 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.128-2262C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779804 | ||||||
| chrX:2779813
|
AT | A | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.128-2248delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2779813 | |||||
| chrX:2779821
|
A | AT | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.128-2240dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2779821 | |||||
| chrX:2779827
|
G | A | 23 | a0001c0001t0001g0287a0001c0001t0001g0315a0001c0001t0003g0047others(20): Show | 23 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.128-2239G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779827 | ||||||
| chrX:2779835
|
C | T | 1 | a0001c0001t0008g0302 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.128-2231C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779835 | ||||||
| chrX:2779936
|
C | T | 1 | a0001c0002t0044g0035 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.128-2130C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779936 | ||||||
| chrX:2780009
|
CA | C | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.128-2054delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780009 | |||||
| chrX:2780019
|
TTATAC | T | 2 | a0001c0001t0003g0061a0001c0001t0005g0022 | 2 | HG01109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.128-2042_128-2038d others(7): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780019 | |||||
| chrX:2780064
|
T | C | 2 | a0001c0001t0001g0290a0001c0001t0002g0294 | 2 | NA19010.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.128-2002T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780064 | ||||||
| chrX:2780067
|
AT | A | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.128-1995delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780067 | |||||
| chrX:2780129
|
G | T | 1 | a0001c0001t0012g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.128-1937G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780129 | ||||||
| chrX:2780150
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.128-1916A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780150 | ||||||
| chrX:2780185
|
A | G | 6 | a0001c0001t0001g0287a0001c0001t0007g0064a0001c0001t0010g0193others(3): Show | 6 | HG02717.hp2 HG02723.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-1881A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780185 | ||||||
| chrX:2780288
|
AAAG | A | 8 | a0002c0008t0037g0098a0003c0004t0001g0226a0003c0004t0001g0227others(5): Show | 8 | HG00099.hp1 HG00140.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-1773_128-1771d others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780288 | |||||
| chrX:2780346
|
C | CA | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.128-1719dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780346 | |||||
| chrX:2780409
|
C | CT | 17 | a0001c0001t0001g0093a0001c0001t0001g0260a0001c0001t0004g0111others(14): Show | 17 | HG01074.hp1 HG01891.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.128-1643dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780409 | |||||
| chrX:2780409
|
CT | C | 19 | a0001c0001t0001g0054a0001c0001t0001g0083a0001c0001t0001g0089others(16): Show | 19 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-1643delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780409 | |||||
| chrX:2780423
|
T | C | 2 | a0001c0001t0001g0189a0001c0001t0004g0068 | 2 | NA19005.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.128-1643T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780423 | ||||||
| chrX:2780424
|
C | T | 7 | a0001c0001t0001g0189a0001c0001t0004g0068a0001c0001t0007g0064others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-1642C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780424 | ||||||
| chrX:2780425
|
T | A | 2 | a0001c0001t0001g0189a0001c0001t0004g0068 | 2 | NA19005.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.128-1641T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780425 | ||||||
| chrX:2780425
|
T | C | 5 | a0001c0001t0007g0064a0001c0001t0010g0193a0001c0001t0022g0191others(2): Show | 5 | HG02717.hp2 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-1641T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780425 | ||||||
| chrX:2780425
|
T | TA | 166 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(163): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.128-1627dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780425 | |||||
| chrX:2780425
|
T | TAA | 8 | a0001c0001t0001g0244a0001c0001t0002g0151a0001c0001t0004g0116others(5): Show | 8 | HG00733.hp1 HG00741.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-1628_128-1627d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780425 | |||||
| chrX:2780425
|
TA | T | 1 | a0001c0001t0003g0073 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.128-1627delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780425 | |||||
| chrX:2780426
|
A | T | 5 | a0001c0001t0007g0064a0001c0001t0010g0193a0001c0001t0022g0191others(2): Show | 5 | HG02717.hp2 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-1640A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780426 | ||||||
| chrX:2780500
|
T | TG | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.128-1563dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780500 | |||||
| chrX:2780692
|
T | TG | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.128-1371dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780692 | |||||
| chrX:2780711
|
C | CT | 1 | a0001c0002t0007g0052 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.128-1354dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780711 | |||||
| chrX:2780716
|
T | TA | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.128-1350_128-1349i others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780716 | ||||||
| chrX:2780717
|
C | A | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.128-1349C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780717 | ||||||
| chrX:2780717
|
C | CA | 5 | a0001c0001t0013g0303a0001c0001t0013g0307a0001c0001t0013g0309others(2): Show | 5 | HG00621.hp1 HG00741.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-1337dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780717 | |||||
| chrX:2780725
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0172 | 2 | NA18963.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.128-1341A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780725 | ||||||
| chrX:2780727
|
AAAG | A | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.128-1332_128-1330d others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780727 | |||||
| chrX:2780728
|
AAG | A | 20 | a0001c0001t0006g0017a0001c0001t0019g0188a0001c0001t0022g0004others(17): Show | 20 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.128-1336_128-1335d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780728 | |||||
| chrX:2780729
|
AG | A | 2 | a0001c0001t0005g0288a0001c0002t0007g0276 | 2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.128-1336delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780729 | ||||||
| chrX:2780754
|
GA | G | 1 | a0001c0001t0004g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.128-1309delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780754 | |||||
| chrX:2780844
|
CT | C | 1 | a0001c0001t0004g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.128-1220delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780844 | |||||
| chrX:2780872
|
CA | C | 2 | a0001c0001t0001g0224a0001c0001t0004g0126 | 2 | NA18961.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.128-1191delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780872 | |||||
| chrX:2780882
|
G | A | 14 | a0001c0001t0001g0093a0001c0001t0005g0288a0001c0001t0019g0188others(11): Show | 14 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.128-1184G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780882 | ||||||
| chrX:2780912
|
AG | A | 1 | a0001c0001t0002g0072 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.128-1148delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780912 | |||||
| chrX:2780913
|
G | A | 31 | a0001c0001t0001g0093a0001c0001t0001g0287a0001c0001t0005g0030others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.128-1153G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780913 | ||||||
| chrX:2780992
|
TG | T | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.128-1069delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780992 | |||||
| chrX:2781005
|
AT | A | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.128-1058delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2781005 | |||||
| chrX:2781069
|
GC | G | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.128-995delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2781069 | |||||
| chrX:2781146
|
T | C | 138 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(135): Show | 138 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.128-920T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781146 | ||||||
| chrX:2781147
|
G | C | 136 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(133): Show | 136 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.128-919G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781147 | ||||||
| chrX:2781148
|
T | C | 136 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(133): Show | 136 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.128-918T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781148 | ||||||
| chrX:2781153
|
C | CAAAGGCT others(3): Show |
1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.128-911_128-902dup others(10): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2781153 | |||||
| chrX:2781191
|
TC | T | 1 | a0001c0001t0004g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.128-872delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2781191 | |||||
| chrX:2781205
|
C | A | 83 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.128-861C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781205 | ||||||
| chrX:2781234
|
T | G | 162 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0032others(159): Show | 162 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.128-832T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781234 | ||||||
| chrX:2781309
|
A | T | 119 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(116): Show | 119 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.128-757A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781309 | ||||||
| chrX:2781319
|
T | C | 111 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(108): Show | 111 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.128-747T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781319 | ||||||
| chrX:2781409
|
A | C | 103 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(100): Show | 103 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.128-657A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781409 | ||||||
| chrX:2781514
|
C | A | 174 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(171): Show | 174 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.128-552C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781514 | ||||||
| chrX:2781584
|
A | G | 15 | a0001c0001t0001g0315a0001c0001t0003g0047a0001c0001t0003g0048others(12): Show | 15 | HG00741.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.128-482A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781584 | ||||||
| chrX:2781604
|
G | T | 7 | a0003c0004t0001g0226a0003c0004t0001g0227a0003c0004t0002g0058others(4): Show | 7 | HG00099.hp1 HG00140.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-462G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781604 | ||||||
| chrX:2781629
|
TC | T | 1 | a0001c0001t0004g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.128-433delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2781629 | |||||
| chrX:2781635
|
G | A | 104 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(101): Show | 104 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.128-431G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781635 | ||||||
| chrX:2781642
|
G | A | 1 | a0001c0002t0034g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.128-424G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781642 | ||||||
| chrX:2781857
|
C | CT | 102 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(99): Show | 102 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.128-200dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2781857 | |||||
| chrX:2781865
|
T | G | 9 | a0001c0001t0001g0315a0001c0001t0003g0047a0001c0001t0003g0048others(6): Show | 9 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-201T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781865 | ||||||
| chrX:2781869
|
GT | G | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.128-194delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2781869 | |||||
| chrX:2781927
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(153): Show | 157 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.128-139A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781927 | ||||||
| chrX:2781975
|
GA | G | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.128-90delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781975 | ||||||
| chrX:2781986
|
T | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(141): Show | 145 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.128-80T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781986 | ||||||
| chrX:2781994
|
T | TG | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.128-72_128-71insG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781994 | ||||||
| chrX:2782027
|
AT | A | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.128-35delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2782027 | |||||
| chrX:2782059
|
TC | T | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | splice_region_variant&intron_variant | LOW | c.128-5delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2782059 | |||||
| chrX:2782148
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.190+20A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782148 | ||||||
| chrX:2782153
|
C | G | 1 | a0001c0001t0014g0207 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.190+25C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782153 | ||||||
| chrX:2782161
|
A | G | 122 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.190+33A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782161 | ||||||
| chrX:2782261
|
T | A | 119 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(116): Show | 119 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.190+133T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782261 | ||||||
| chrX:2782270
|
TG | T | 1 | a0001c0001t0004g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.190+148delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2782270 | |||||
| chrX:2782287
|
TC | T | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.190+161delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2782287 | |||||
| chrX:2782313
|
TC | T | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.190+188delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2782313 | |||||
| chrX:2782368
|
GT | G | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.190+242delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2782368 | |||||
| chrX:2782386
|
C | G | 1 | a0001c0002t0007g0052 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.190+258C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782386 | ||||||
| chrX:2782415
|
GA | G | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.190+289delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2782415 | |||||
| chrX:2782504
|
TG | T | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.190+380delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2782504 | |||||
| chrX:2782567
|
C | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(122): Show | 126 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.190+439C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782567 | ||||||
| chrX:2782572
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(132): Show | 136 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.190+444A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782572 | ||||||
| chrX:2782592
|
G | T | 1 | a0001c0001t0024g0184 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.190+464G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782592 | ||||||
| chrX:2782597
|
T | G | 3 | a0001c0001t0027g0026a0002c0008t0037g0098a0004c0009t0035g0282 | 3 | HG02922.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.190+469T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782597 | ||||||
| chrX:2782735
|
T | C | 2 | a0001c0001t0004g0053a0001c0001t0004g0153 | 2 | HG02071.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.190+607T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782735 | ||||||
| chrX:2782751
|
AC | A | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.190+628delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2782751 | |||||
| chrX:2782767
|
TG | T | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.190+643delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2782767 | |||||
| chrX:2782880
|
G | C | 1 | a0001c0001t0021g0021 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.190+752G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782880 | ||||||
| chrX:2782931
|
C | T | 3 | a0001c0001t0013g0303a0001c0001t0013g0307a0001c0001t0013g0309 | 3 | HG01884.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.190+803C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782931 | ||||||
| chrX:2782963
|
T | C | 24 | a0001c0001t0001g0015a0001c0001t0001g0093a0001c0001t0001g0134others(21): Show | 24 | HG00741.hp1 HG01109.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.190+835T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782963 | ||||||
| chrX:2783032
|
T | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(238): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.190+904T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783032 | ||||||
| chrX:2783042
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.190+914A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783042 | ||||||
| chrX:2783048
|
T | TC | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.190+922dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2783048 | |||||
| chrX:2783052
|
C | CA | 1 | a0001c0001t0021g0021 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.190+925dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2783052 | |||||
| chrX:2783100
|
AT | A | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.190+974delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2783100 | |||||
| chrX:2783144
|
C | T | 268 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(265): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.190+1016C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783144 | ||||||
| chrX:2783188
|
TC | T | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.190+1063delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2783188 | |||||
| chrX:2783203
|
T | C | 1 | a0001c0001t0004g0245 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.190+1075T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783203 | ||||||
| chrX:2783314
|
C | CA | 142 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0037others(139): Show | 142 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.190+1192dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2783314 | |||||
| chrX:2783354
|
A | AG | 7 | a0001c0001t0001g0086a0001c0001t0001g0115a0001c0001t0001g0224others(4): Show | 7 | HG00438.hp2 HG01978.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.190+1232dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2783354 | |||||
| chrX:2783418
|
T | C | 1 | a0001c0001t0001g0015 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.190+1290T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783418 | ||||||
| chrX:2783442
|
A | G | 2 | a0001c0002t0005g0128a0004c0009t0035g0282 | 2 | HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.190+1314A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783442 | ||||||
| chrX:2783591
|
G | A | 2 | a0001c0001t0014g0207a0001c0001t0016g0277 | 2 | HG03239.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.190+1463G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783591 | ||||||
| chrX:2783658
|
A | C | 2 | a0001c0001t0001g0304a0001c0002t0008g0321 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.190+1530A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783658 | ||||||
| chrX:2783702
|
TG | T | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.190+1579delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2783702 | |||||
| chrX:2783732
|
TG | T | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.190+1607delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2783732 | |||||
| chrX:2783795
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0093a0001c0001t0021g0021others(2): Show | 5 | HG00741.hp1 HG02970.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.190+1667C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783795 | ||||||
| chrX:2783804
|
G | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0093a0001c0001t0021g0021others(2): Show | 5 | HG00741.hp1 HG02970.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.190+1676G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783804 | ||||||
| chrX:2783897
|
T | C | 2 | a0001c0001t0001g0304a0001c0005t0015g0051 | 2 | HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.190+1769T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783897 | ||||||
| chrX:2783931
|
T | C | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.190+1803T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783931 | ||||||
| chrX:2783974
|
GA | G | 1 | a0001c0001t0004g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.190+1851delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2783974 | |||||
| chrX:2783976
|
AAAACC | A | 5 | a0001c0001t0001g0090a0001c0001t0001g0110a0001c0001t0001g0304others(2): Show | 5 | HG02129.hp2 HG03453.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+1873_190+1877d others(7): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2783976 | |||||
| chrX:2784001
|
C | A | 4 | a0001c0001t0001g0304a0001c0001t0008g0302a0001c0001t0025g0317others(1): Show | 4 | HG01884.hp2 HG03453.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+1873C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784001 | ||||||
| chrX:2784001
|
CA | C | 1 | a0001c0001t0004g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.190+1876delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2784001 | |||||
| chrX:2784001
|
CAAACA | C | 1 | a0001c0001t0028g0130 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.190+1883_190+1887d others(7): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2784001 | |||||
| chrX:2784005
|
CA | C | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.190+1881delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2784005 | |||||
| chrX:2784006
|
A | C | 126 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0032others(123): Show | 126 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.190+1878A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784006 | ||||||
| chrX:2784007
|
A | C | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.190+1879A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784007 | ||||||
| chrX:2784034
|
C | A | 1 | a0001c0002t0012g0049 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.190+1906C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784034 | ||||||
| chrX:2784073
|
TC | T | 1 | a0001c0001t0004g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.190+1950delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2784073 | |||||
| chrX:2784102
|
T | C | 111 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(108): Show | 111 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.190+1974T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784102 | ||||||
| chrX:2784189
|
TG | T | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.190+2064delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2784189 | |||||
| chrX:2784298
|
T | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0135others(11): Show | 15 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.190+2170T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784298 | ||||||
| chrX:2784350
|
AG | A | 1 | a0001c0001t0003g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.190+2224delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2784350 | |||||
| chrX:2784429
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.190+2301A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784429 | ||||||
| chrX:2784439
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.190+2311C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784439 | ||||||
| chrX:2784527
|
G | A | 64 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0041others(61): Show | 64 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.190+2399G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784527 | ||||||
| chrX:2784564
|
C | T | 8 | a0001c0001t0005g0003a0001c0001t0005g0029a0001c0001t0005g0119others(5): Show | 8 | HG01074.hp1 HG01261.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.190+2436C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784564 | ||||||
| chrX:2784569
|
C | CA | 1 | a0001c0001t0003g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.190+2458dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2784569 | |||||
| chrX:2784569
|
CA | C | 5 | a0001c0001t0001g0054a0001c0001t0001g0118a0001c0001t0001g0172others(2): Show | 5 | HG02165.hp2 HG03491.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+2458delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2784569 | |||||
| chrX:2784569
|
CAAA | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(96): Show | 100 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.190+2456_190+2458d others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2784569 | |||||
| chrX:2784657
|
C | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0134others(22): Show | 26 | HG00642.hp1 HG00741.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.190+2529C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784657 | ||||||
| chrX:2784734
|
AC | A | 1 | a0001c0001t0004g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.190+2612delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2784734 | |||||
| chrX:2784738
|
C | T | 1 | a0001c0001t0006g0025 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.190+2610C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784738 | ||||||
| chrX:2784758
|
C | G | 78 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0041others(75): Show | 78 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.190+2630C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784758 | ||||||
| chrX:2784905
|
G | T | 77 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0041others(74): Show | 77 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.190+2777G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784905 | ||||||
| chrX:2785130
|
G | C | 1 | a0001c0001t0002g0217 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.190+3002G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785130 | ||||||
| chrX:2785142
|
T | TC | 1 | a0001c0001t0004g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.190+3014_190+3015i others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785142 | ||||||
| chrX:2785164
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.190+3036C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785164 | ||||||
| chrX:2785248
|
AT | A | 1 | a0001c0001t0004g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.190+3125delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2785248 | |||||
| chrX:2785313
|
G | C | 64 | a0001c0001t0001g0041a0001c0001t0001g0057a0001c0001t0001g0083others(61): Show | 64 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.190+3185G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785313 | ||||||
| chrX:2785332
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.190+3204C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785332 | ||||||
| chrX:2785350
|
T | C | 174 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0041others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.190+3222T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785350 | ||||||
| chrX:2785459
|
A | AT | 105 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0054others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.190+3331_190+3332i others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785459 | ||||||
| chrX:2785460
|
A | AT | 65 | a0001c0001t0001g0041a0001c0001t0001g0057a0001c0001t0001g0083others(62): Show | 65 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.190+3339dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2785460 | |||||
| chrX:2785460
|
A | T | 105 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0054others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.190+3332A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785460 | ||||||
| chrX:2785493
|
TG | T | 1 | a0001c0001t0004g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.190+3368delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2785493 | |||||
| chrX:2785503
|
A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.190+3375A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785503 | ||||||
| chrX:2785513
|
CT | C | 1 | a0001c0001t0004g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.190+3394delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2785513 | |||||
| chrX:2785592
|
A | G | 170 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0041others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.190+3464A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785592 | ||||||
| chrX:2785649
|
GA | G | 1 | a0001c0001t0004g0126 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.190+3525delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2785649 | |||||
| chrX:2785856
|
T | G | 1 | a0001c0001t0004g0068 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.190+3728T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785856 | ||||||
| chrX:2786016
|
G | A | 2 | a0001c0001t0001g0214a0001c0001t0001g0287 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.191-3628G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786016 | ||||||
| chrX:2786260
|
C | CT | 17 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0214others(14): Show | 17 | HG00741.hp1 HG01243.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.191-3367dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | |||||
| chrX:2786260
|
C | CTT | 2 | a0001c0001t0001g0093a0001c0001t0036g0002 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.191-3368_191-3367d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | |||||
| chrX:2786260
|
C | CTTTTTTT others(2): Show |
8 | a0001c0001t0001g0104a0001c0001t0001g0251a0001c0001t0004g0167others(5): Show | 8 | HG01168.hp1 HG01517.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.191-3375_191-3367d others(11): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | |||||
| chrX:2786260
|
C | CTTTTTTT others(3): Show |
66 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0032others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.191-3376_191-3367d others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | |||||
| chrX:2786260
|
C | CTTTTTTT others(4): Show |
29 | a0001c0001t0001g0220a0001c0001t0001g0232a0001c0001t0001g0234others(26): Show | 29 | HG00738.hp2 HG01099.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.191-3377_191-3367d others(13): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | |||||
| chrX:2786260
|
C | CTTTTTTT others(10): Show |
4 | a0001c0001t0005g0145a0001c0002t0034g0010a0001c0002t0041g0140others(1): Show | 4 | HG02717.hp2 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-3383_191-3367d others(19): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | |||||
| chrX:2786260
|
C | CTTTTTTT others(11): Show |
29 | a0001c0001t0001g0041a0001c0001t0001g0057a0001c0001t0001g0099others(26): Show | 29 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.191-3367_191-3366i others(20): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | |||||
| chrX:2786260
|
C | CTTTTTTT others(12): Show |
15 | a0001c0001t0001g0083a0001c0001t0001g0102a0001c0001t0001g0139others(12): Show | 15 | HG00323.hp2 HG02486.hp1 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.191-3367_191-3366i others(21): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | |||||
| chrX:2786260
|
C | CTTTTTTT others(13): Show |
10 | a0001c0001t0001g0103a0001c0001t0001g0142a0001c0001t0003g0063others(7): Show | 10 | HG01975.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.191-3367_191-3366i others(22): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | |||||
| chrX:2786260
|
C | CTTTTTTT others(15): Show |
2 | a0001c0001t0003g0201a0001c0002t0005g0034 | 2 | HG02970.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.191-3367_191-3366i others(24): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | |||||
| chrX:2786260
|
CT | C | 12 | a0001c0001t0001g0038a0001c0001t0002g0072a0001c0001t0002g0294others(9): Show | 12 | HG01074.hp1 HG01261.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.191-3367delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | |||||
| chrX:2786260
|
CTT | C | 1 | a0001c0001t0001g0196 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.191-3368_191-3367d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | |||||
| chrX:2786294
|
G | C | 167 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0032others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.191-3350G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786294 | ||||||
| chrX:2786428
|
T | C | 189 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.191-3216T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786428 | ||||||
| chrX:2786483
|
G | A | 15 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0005g0020others(12): Show | 15 | HG00741.hp1 HG01243.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.191-3161G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786483 | ||||||
| chrX:2786498
|
C | T | 1 | a0001c0002t0007g0052 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.191-3146C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786498 | ||||||
| chrX:2786515
|
A | G | 189 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.191-3129A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786515 | ||||||
| chrX:2786568
|
T | C | 189 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.191-3076T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786568 | ||||||
| chrX:2786759
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.191-2885G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786759 | ||||||
| chrX:2786767
|
T | C | 190 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.191-2877T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786767 | ||||||
| chrX:2786827
|
A | G | 1 | a0001c0001t0002g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.191-2817A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786827 | ||||||
| chrX:2786948
|
T | C | 179 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.191-2696T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786948 | ||||||
| chrX:2786970
|
C | T | 13 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0135others(10): Show | 14 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.191-2674C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786970 | ||||||
| chrX:2787109
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0036g0002 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.191-2535C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787109 | ||||||
| chrX:2787163
|
A | G | 7 | a0001c0001t0005g0003a0001c0001t0005g0029a0001c0001t0005g0119others(4): Show | 7 | HG01074.hp1 HG01261.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.191-2481A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787163 | ||||||
| chrX:2787224
|
C | T | 13 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0135others(10): Show | 14 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.191-2420C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787224 | ||||||
| chrX:2787247
|
C | G | 1 | a0004c0009t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-2397C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787247 | ||||||
| chrX:2787367
|
A | G | 1 | a0004c0009t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-2277A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787367 | ||||||
| chrX:2787413
|
A | G | 1 | a0004c0009t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-2231A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787413 | ||||||
| chrX:2787421
|
G | A | 60 | a0001c0001t0001g0041a0001c0001t0001g0057a0001c0001t0001g0083others(57): Show | 60 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.191-2223G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787421 | ||||||
| chrX:2787423
|
T | A | 127 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.191-2221T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787423 | ||||||
| chrX:2787439
|
C | T | 2 | a0001c0001t0010g0193a0001c0001t0020g0131 | 2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.191-2205C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787439 | ||||||
| chrX:2787556
|
CTGTT | C | 1 | a0001c0001t0001g0212 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.191-2085_191-2082d others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2787556 | |||||
| chrX:2787582
|
C | T | 1 | a0004c0009t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-2062C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787582 | ||||||
| chrX:2787732
|
C | A | 1 | a0001c0001t0001g0169 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.191-1912C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787732 | ||||||
| chrX:2787809
|
G | A | 1 | a0004c0009t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-1835G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787809 | ||||||
| chrX:2787822
|
G | A | 1 | a0004c0009t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-1822G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787822 | ||||||
| chrX:2787838
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0107 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.191-1806C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787838 | ||||||
| chrX:2787864
|
GCCACTGC others(170): Show |
G | 2 | a0001c0001t0021g0021a0002c0003t0031g0109 | 2 | HG00741.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.191-1754_191-1578d others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2787864 | |||||
| chrX:2787894
|
C | CA | 1 | a0001c0001t0005g0271 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.191-1746dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2787894 | |||||
| chrX:2787907
|
C | CA | 5 | a0001c0001t0001g0090a0001c0001t0001g0104a0001c0001t0001g0105others(2): Show | 5 | HG03942.hp1 NA18946.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.191-1718dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2787907 | |||||
| chrX:2787907
|
CA | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(152): Show | 156 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.191-1718delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2787907 | |||||
| chrX:2787907
|
CAA | C | 7 | a0001c0001t0001g0074a0001c0001t0001g0304a0001c0001t0002g0272others(4): Show | 7 | HG01070.hp2 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.191-1719_191-1718d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2787907 | |||||
| chrX:2787907
|
CAAA | C | 1 | a0004c0009t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-1720_191-1718d others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2787907 | |||||
| chrX:2788100
|
G | GGAA | 1 | a0001c0001t0001g0070 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.191-1544_191-1543i others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788100 | ||||||
| chrX:2788102
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.191-1542A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788102 | ||||||
| chrX:2788102
|
AAG | A | 72 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0041others(69): Show | 72 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.191-1532_191-1531d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2788102 | |||||
| chrX:2788172
|
G | A | 1 | a0004c0009t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-1472G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788172 | ||||||
| chrX:2788275
|
G | T | 1 | a0001c0002t0034g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.191-1369G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788275 | ||||||
| chrX:2788299
|
G | A | 74 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0041others(71): Show | 74 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.191-1345G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788299 | ||||||
| chrX:2788332
|
C | T | 1 | a0004c0009t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-1312C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788332 | ||||||
| chrX:2788446
|
G | T | 58 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0041others(55): Show | 58 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.191-1198G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788446 | ||||||
| chrX:2788527
|
A | AG | 1 | a0001c0001t0001g0070 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.191-1113dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2788527 | |||||
| chrX:2788745
|
C | G | 1 | a0004c0009t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-899C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788745 | ||||||
| chrX:2788798
|
T | C | 1 | a0004c0009t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-846T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788798 | ||||||
| chrX:2788800
|
A | G | 1 | a0001c0001t0003g0158 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.191-844A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788800 | ||||||
| chrX:2788855
|
T | TA | 184 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.191-779dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2788855 | |||||
| chrX:2788903
|
A | G | 28 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0139others(25): Show | 28 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.191-741A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788903 | ||||||
| chrX:2789019
|
A | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(122): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.191-625A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2789019 | ||||||
| chrX:2789101
|
T | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(144): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.191-543T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2789101 | ||||||
| chrX:2789294
|
A | G | 2 | a0001c0001t0001g0142a0004c0009t0035g0282 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.191-350A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2789294 | ||||||
| chrX:2789330
|
T | C | 2 | a0001c0001t0021g0021a0002c0003t0031g0109 | 2 | HG00741.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.191-314T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2789330 | ||||||
| chrX:2789459
|
T | TAAGTTTA others(14): Show |
62 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0070others(59): Show | 62 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.191-179_191-178ins others(21): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2789459 | |||||
| chrX:2789570
|
A | T | 2 | a0001c0001t0013g0303a0001c0001t0013g0307 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.191-74A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2789570 | ||||||
| chrX:2789729
|
T | TTTTTA | 3 | a0001c0001t0001g0296a0001c0001t0004g0185a0002c0003t0001g0042 | 3 | HG00408.hp2 NA19054.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.253+49_253+53dupTT others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2789729 | |||||
| chrX:2789729
|
T | TTTTTATT others(13): Show |
1 | a0002c0008t0037g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.253+34_253+53dupTT others(18): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2789729 | |||||
| chrX:2789729
|
TTTTTATT others(3): Show |
T | 12 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(9): Show | 12 | HG01168.hp2 HG01169.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.253+44_253+53delTT others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2789729 | |||||
| chrX:2789777
|
A | C | 2 | a0001c0001t0021g0021a0002c0003t0031g0109 | 2 | HG00741.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.253+71A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2789777 | ||||||
| chrX:2789783
|
TTTTAC | T | 61 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0070others(58): Show | 61 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.253+82_253+86delCT others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2789783 | |||||
| chrX:2789796
|
T | G | 2 | a0001c0001t0001g0134a0001c0001t0049g0122 | 2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.253+90T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2789796 | ||||||
| chrX:2789930
|
G | T | 3 | a0001c0001t0013g0303a0001c0001t0013g0307a0001c0001t0013g0309 | 3 | HG01884.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.253+224G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2789930 | ||||||
| chrX:2789937
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(229): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.253+231T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2789937 | ||||||
| chrX:2790001
|
T | C | 14 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(11): Show | 14 | HG01168.hp2 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.253+295T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790001 | ||||||
| chrX:2790062
|
G | T | 13 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0005g0020others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.253+356G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790062 | ||||||
| chrX:2790078
|
G | C | 13 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(10): Show | 13 | HG01168.hp2 HG01169.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.253+372G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790078 | ||||||
| chrX:2790093
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.253+387C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790093 | ||||||
| chrX:2790108
|
C | T | 2 | a0001c0001t0021g0021a0002c0003t0031g0109 | 2 | HG00741.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.253+402C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790108 | ||||||
| chrX:2790270
|
G | A | 1 | a0001c0001t0009g0031 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.253+564G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790270 | ||||||
| chrX:2790424
|
C | T | 1 | a0002c0008t0037g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.253+718C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790424 | ||||||
| chrX:2790490
|
C | A | 17 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(14): Show | 17 | HG01168.hp2 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.253+784C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790490 | ||||||
| chrX:2790505
|
G | GA | 235 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.253+816dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2790505 | |||||
| chrX:2790505
|
G | GAA | 4 | a0001c0001t0001g0114a0001c0001t0001g0213a0001c0001t0004g0195others(1): Show | 4 | HG02109.hp1 HG03688.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.253+815_253+816dup others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2790505 | |||||
| chrX:2790610
|
G | A | 40 | a0001c0001t0001g0070a0001c0001t0001g0114a0001c0001t0001g0134others(37): Show | 40 | HG00438.hp1 HG00558.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.253+904G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790610 | ||||||
| chrX:2790674
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.253+968C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790674 | ||||||
| chrX:2790706
|
A | C | 2 | a0001c0001t0001g0183a0001c0001t0004g0068 | 2 | HG02273.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.253+1000A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790706 | ||||||
| chrX:2790712
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.253+1006A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790712 | ||||||
| chrX:2790810
|
C | CG | 3 | a0001c0001t0001g0070a0001c0001t0001g0224a0001c0001t0028g0279 | 3 | HG00438.hp2 NA19062.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.253+1111dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2790810 | |||||
| chrX:2790864
|
A | G | 3 | a0001c0001t0020g0138a0001c0001t0021g0278a0001c0005t0015g0045 | 3 | HG02109.hp2 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.253+1158A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790864 | ||||||
| chrX:2790967
|
ATAAATT | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.253+1267_253+1272d others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2790967 | |||||
| chrX:2791052
|
TTTC | T | 30 | a0001c0001t0001g0070a0001c0001t0001g0114a0001c0001t0001g0157others(27): Show | 30 | HG00438.hp1 HG00558.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.253+1349_253+1351d others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2791052 | |||||
| chrX:2791058
|
G | GT | 2 | a0001c0001t0001g0304a0001c0001t0010g0050 | 2 | HG02602.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.253+1363dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2791058 | |||||
| chrX:2791058
|
GT | G | 1 | a0002c0008t0037g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.253+1363delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2791058 | |||||
| chrX:2791183
|
C | T | 15 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(12): Show | 15 | HG01168.hp2 HG01169.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.253+1477C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2791183 | ||||||
| chrX:2791247
|
T | TG | 1 | a0001c0001t0001g0070 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.253+1545dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2791247 | |||||
| chrX:2791290
|
T | A | 1 | a0002c0008t0037g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.253+1584T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2791290 | ||||||
| chrX:2791348
|
A | AG | 1 | a0001c0001t0001g0070 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.253+1644dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2791348 | |||||
| chrX:2791524
|
CTCCAAAA others(13): Show |
C | 7 | a0001c0001t0001g0209a0001c0001t0001g0213a0001c0001t0001g0249others(4): Show | 7 | HG01123.hp2 HG01433.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.253+1822_253+1841d others(22): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2791524 | |||||
| chrX:2791559
|
C | T | 1 | a0001c0001t0002g0314 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.253+1853C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2791559 | ||||||
| chrX:2792059
|
G | A | 1 | a0001c0001t0005g0020 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.253+2353G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792059 | ||||||
| chrX:2792165
|
A | G | 2 | a0001c0001t0005g0145a0001c0005t0015g0051 | 2 | HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.254-2370A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792165 | ||||||
| chrX:2792222
|
G | C | 1 | a0001c0007t0032g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.254-2313G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792222 | ||||||
| chrX:2792270
|
T | C | 1 | a0002c0008t0037g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.254-2265T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792270 | ||||||
| chrX:2792297
|
C | G | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.254-2238C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792297 | ||||||
| chrX:2792331
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.254-2204C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792331 | ||||||
| chrX:2792356
|
T | A | 1 | a0002c0008t0037g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.254-2179T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792356 | ||||||
| chrX:2792380
|
G | C | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.254-2155G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792380 | ||||||
| chrX:2792446
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.254-2089G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792446 | ||||||
| chrX:2792463
|
T | G | 6 | a0001c0001t0001g0209a0001c0001t0001g0213a0001c0001t0001g0249others(3): Show | 6 | HG01433.hp2 HG02004.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.254-2072T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792463 | ||||||
| chrX:2792465
|
G | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(163): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.254-2070G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792465 | ||||||
| chrX:2792517
|
TTTTCTTT others(3): Show |
T | 1 | a0002c0003t0001g0028 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.254-2004_254-1995d others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2792517 | |||||
| chrX:2792545
|
T | TTGTG | 151 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(148): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.254-1968_254-1965d others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2792545 | |||||
| chrX:2792545
|
T | TTGTGTG | 3 | a0001c0001t0001g0016a0001c0001t0001g0265a0001c0001t0006g0254 | 3 | NA18950.hp2 NA19083.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.254-1970_254-1965d others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2792545 | |||||
| chrX:2792545
|
T | TTGTGTGT others(1): Show |
2 | a0001c0001t0001g0251a0001c0001t0003g0283 | 2 | HG03704.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.254-1972_254-1965d others(10): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2792545 | |||||
| chrX:2792545
|
T | TTGTGTGT others(3): Show |
12 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(9): Show | 12 | HG01168.hp2 HG01169.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.254-1974_254-1965d others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2792545 | |||||
| chrX:2792545
|
T | TTGTGTGT others(7): Show |
2 | a0001c0001t0019g0188a0001c0001t0046g0123 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.254-1978_254-1965d others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2792545 | |||||
| chrX:2792545
|
TTG | T | 3 | a0001c0001t0001g0267a0001c0001t0002g0174a0001c0001t0028g0130 | 3 | HG00621.hp1 NA19084.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.254-1966_254-1965d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2792545 | |||||
| chrX:2792799
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.254-1736C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792799 | ||||||
| chrX:2792846
|
G | C | 4 | a0001c0001t0013g0303a0001c0001t0013g0307a0001c0001t0013g0309others(1): Show | 4 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.254-1689G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792846 | ||||||
| chrX:2792921
|
G | GT | 1 | a0001c0001t0002g0181 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.254-1604dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2792921 | |||||
| chrX:2792954
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.254-1581C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792954 | ||||||
| chrX:2793146
|
C | T | 14 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(11): Show | 14 | HG01168.hp2 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.254-1389C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2793146 | ||||||
| chrX:2793198
|
C | T | 3 | a0001c0001t0001g0142a0001c0001t0021g0021a0002c0003t0031g0109 | 3 | HG00741.hp1 HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.254-1337C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2793198 | ||||||
| chrX:2793388
|
G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.254-1147G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2793388 | ||||||
| chrX:2793425
|
A | G | 3 | a0001c0001t0013g0303a0001c0001t0013g0307a0001c0001t0013g0309 | 3 | HG01884.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.254-1110A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2793425 | ||||||
| chrX:2793681
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(118): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.254-854C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2793681 | ||||||
| chrX:2793682
|
G | A | 6 | a0001c0001t0003g0283a0001c0001t0007g0064a0001c0001t0012g0289others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.254-853G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2793682 | ||||||
| chrX:2793738
|
G | C | 1 | a0001c0001t0001g0251 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.254-797G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2793738 | ||||||
| chrX:2793770
|
A | G | 1 | a0001c0001t0009g0246 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.254-765A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2793770 | ||||||
| chrX:2793865
|
TG | T | 1 | a0005c0006t0001g0112 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.254-668delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2793865 | |||||
| chrX:2793895
|
TG | T | 1 | a0005c0006t0001g0112 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.254-636delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2793895 | |||||
| chrX:2793920
|
G | C | 39 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(36): Show | 39 | HG00741.hp1 HG01167.hp1 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.254-615G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2793920 | ||||||
| chrX:2794211
|
T | TC | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.254-322dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2794211 | |||||
| chrX:2794242
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(123): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.254-293C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2794242 | ||||||
| chrX:2794265
|
C | CA | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.254-270_254-269ins others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2794265 | ||||||
| chrX:2794288
|
AG | A | 1 | a0005c0006t0001g0112 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.254-243delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2794288 | |||||
| chrX:2794344
|
G | A | 1 | a0002c0008t0037g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.254-191G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2794344 | ||||||
| chrX:2794364
|
G | GC | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.254-169dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2794364 | |||||
| chrX:2794488
|
A | AC | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.254-45dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2794488 | |||||
| chrX:2794615
|
G | GC | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.322+14dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2794615 | |||||
| chrX:2794620
|
C | T | 36 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(33): Show | 36 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.322+17C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2794620 | ||||||
| chrX:2794666
|
G | GC | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.322+65dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2794666 | |||||
| chrX:2794679
|
G | T | 1 | a0001c0001t0002g0262 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.322+76G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2794679 | ||||||
| chrX:2794869
|
C | T | 1 | a0002c0003t0031g0109 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.322+266C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2794869 | ||||||
| chrX:2794884
|
A | AG | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.322+282dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2794884 | |||||
| chrX:2794971
|
T | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.322+368T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2794971 | ||||||
| chrX:2795028
|
G | A | 163 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.322+425G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795028 | ||||||
| chrX:2795032
|
C | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(166): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.322+429C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795032 | ||||||
| chrX:2795048
|
A | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.322+445A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795048 | ||||||
| chrX:2795098
|
T | C | 34 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(31): Show | 34 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.322+495T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795098 | ||||||
| chrX:2795147
|
T | A | 1 | a0001c0005t0015g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.322+544T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795147 | ||||||
| chrX:2795170
|
G | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.322+567G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795170 | ||||||
| chrX:2795221
|
G | GC | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.322+619dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2795221 | |||||
| chrX:2795240
|
G | GTATT | 180 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.322+640_322+641ins others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2795240 | |||||
| chrX:2795253
|
G | A | 1 | a0001c0002t0008g0321 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.322+650G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795253 | ||||||
| chrX:2795343
|
A | AT | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.322+741dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2795343 | |||||
| chrX:2795482
|
CAT | C | 22 | a0001c0001t0001g0139a0001c0001t0003g0283a0001c0001t0007g0064others(19): Show | 22 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.322+882_322+883del others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2795482 | |||||
| chrX:2795491
|
ATATCTT | A | 33 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(30): Show | 33 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.322+892_322+897del others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2795491 | |||||
| chrX:2795526
|
C | T | 2 | a0001c0001t0019g0188a0001c0001t0046g0123 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.322+923C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795526 | ||||||
| chrX:2795547
|
G | C | 1 | a0001c0001t0025g0027 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.322+944G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795547 | ||||||
| chrX:2795561
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.322+958A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795561 | ||||||
| chrX:2795657
|
G | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.322+1054G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795657 | ||||||
| chrX:2795667
|
A | T | 1 | a0001c0001t0026g0210 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.322+1064A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795667 | ||||||
| chrX:2795671
|
T | A | 3 | a0001c0001t0007g0064a0001c0001t0012g0289a0001c0001t0048g0121 | 3 | HG01891.hp2 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.322+1068T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795671 | ||||||
| chrX:2795681
|
C | T | 1 | a0001c0001t0003g0240 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.322+1078C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795681 | ||||||
| chrX:2795722
|
A | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.322+1119A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795722 | ||||||
| chrX:2795753
|
G | T | 1 | a0001c0001t0002g0040 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.322+1150G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795753 | ||||||
| chrX:2795766
|
T | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.322+1163T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795766 | ||||||
| chrX:2795768
|
C | CT | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.322+1166dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2795768 | |||||
| chrX:2795769
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.322+1166T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795769 | ||||||
| chrX:2795850
|
G | GT | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.322+1250dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2795850 | |||||
| chrX:2795915
|
C | CA | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.322+1315dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2795915 | |||||
| chrX:2795935
|
C | T | 2 | a0001c0001t0019g0188a0001c0001t0046g0123 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.322+1332C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795935 | ||||||
| chrX:2795995
|
A | C | 2 | a0001c0001t0003g0202a0001c0001t0003g0215 | 2 | NA18998.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.323-1315A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795995 | ||||||
| chrX:2796044
|
G | GTA | 34 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(31): Show | 34 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.323-1264_323-1263d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796044 | |||||
| chrX:2796070
|
T | C | 2 | a0001c0001t0019g0188a0001c0001t0046g0123 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.323-1240T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796070 | ||||||
| chrX:2796099
|
ATATCTT | A | 1 | a0001c0001t0001g0142 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.323-1207_323-1202d others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796099 | |||||
| chrX:2796121
|
A | G | 33 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(30): Show | 33 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.323-1189A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796121 | ||||||
| chrX:2796153
|
A | AT | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.323-1154dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796153 | |||||
| chrX:2796212
|
CATAA | C | 33 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(30): Show | 33 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.323-1094_323-1091d others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796212 | |||||
| chrX:2796225
|
A | AT | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.323-1084dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796225 | |||||
| chrX:2796236
|
C | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.323-1074C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796236 | ||||||
| chrX:2796275
|
A | AT | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.323-1034dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796275 | |||||
| chrX:2796303
|
G | C | 1 | a0001c0001t0001g0169 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.323-1007G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796303 | ||||||
| chrX:2796306
|
T | TA | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.323-1001dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796306 | |||||
| chrX:2796320
|
TA | T | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.323-987delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796320 | |||||
| chrX:2796468
|
A | ATG | 3 | a0001c0001t0001g0304a0001c0002t0044g0035a0002c0008t0037g0098 | 3 | HG03453.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.323-822_323-821dup others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796468 | |||||
| chrX:2796468
|
A | ATGTG | 2 | a0001c0001t0001g0015a0001c0001t0004g0111 | 2 | NA19030.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.323-824_323-821dup others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796468 | |||||
| chrX:2796468
|
A | ATGTGTG | 120 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(117): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.323-826_323-821dup others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796468 | |||||
| chrX:2796468
|
A | ATGTGTGT others(1): Show |
7 | a0001c0001t0001g0074a0001c0001t0001g0315a0001c0001t0002g0149others(4): Show | 7 | HG00741.hp1 HG01099.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.323-828_323-821dup others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796468 | |||||
| chrX:2796468
|
A | ATGTGTGT others(3): Show |
15 | a0001c0001t0005g0020a0001c0001t0005g0046a0001c0001t0013g0303others(12): Show | 15 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.323-830_323-821dup others(10): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796468 | |||||
| chrX:2796490
|
A | ATGTGTGT others(1): Show |
33 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(30): Show | 33 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.323-819_323-818ins others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796490 | |||||
| chrX:2796490
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.323-820A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796490 | ||||||
| chrX:2796492
|
A | G | 42 | a0001c0001t0001g0032a0001c0001t0001g0074a0001c0001t0001g0093others(39): Show | 42 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.323-818A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796492 | ||||||
| chrX:2796494
|
A | G | 36 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(33): Show | 36 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.323-816A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796494 | ||||||
| chrX:2796539
|
CAT | C | 1 | a0001c0001t0002g0259 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.323-765_323-764del others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796539 | |||||
| chrX:2796543
|
T | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0002g0129others(2): Show | 5 | HG00099.hp2 HG01070.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.323-767T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796543 | ||||||
| chrX:2796696
|
A | G | 1 | a0002c0003t0031g0109 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.323-614A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796696 | ||||||
| chrX:2796715
|
T | C | 33 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(30): Show | 33 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.323-595T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796715 | ||||||
| chrX:2796863
|
G | A | 2 | a0001c0001t0019g0188a0001c0001t0046g0123 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.323-447G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796863 | ||||||
| chrX:2796884
|
G | A | 1 | a0001c0001t0001g0290 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.323-426G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796884 | ||||||
| chrX:2796924
|
G | A | 35 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(32): Show | 35 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.323-386G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796924 | ||||||
| chrX:2797145
|
C | A | 5 | a0001c0001t0019g0188a0001c0001t0021g0021a0001c0001t0046g0123others(2): Show | 5 | HG00741.hp1 HG02970.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.323-165C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2797145 | ||||||
| chrX:2797283
|
C | T | 33 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(30): Show | 33 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.323-27C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2797283 | ||||||
| chrX:2797379
|
A | C | 1 | a0001c0001t0019g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.373+19A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2797379 | ||||||
| chrX:2797384
|
A | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.373+24A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2797384 | ||||||
| chrX:2797422
|
C | T | 1 | a0001c0001t0002g0247 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.373+62C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2797422 | ||||||
| chrX:2797514
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.373+154G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2797514 | ||||||
| chrX:2797586
|
G | GCA | 38 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(35): Show | 38 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.373+248_373+249dup others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2797586 | |||||
| chrX:2797759
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.373+399C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2797759 | ||||||
| chrX:2797789
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0304 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.373+429T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2797789 | ||||||
| chrX:2797829
|
T | G | 35 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(32): Show | 35 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.373+469T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2797829 | ||||||
| chrX:2797936
|
A | T | 2 | a0001c0001t0019g0188a0001c0001t0046g0123 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.373+576A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2797936 | ||||||
| chrX:2797958
|
T | G | 2 | a0001c0001t0019g0188a0001c0001t0046g0123 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.373+598T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2797958 | ||||||
| chrX:2798159
|
T | G | 2 | a0001c0001t0001g0134a0001c0001t0049g0122 | 2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.373+799T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2798159 | ||||||
| chrX:2798305
|
G | A | 35 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(32): Show | 35 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.373+945G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2798305 | ||||||
| chrX:2798364
|
CTTTTCT | C | 2 | a0001c0001t0019g0188a0001c0001t0046g0123 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.373+1009_373+1014d others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2798364 | |||||
| chrX:2798369
|
C | CT | 48 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0114others(45): Show | 49 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.373+1029dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2798369 | |||||
| chrX:2798369
|
C | CTT | 2 | a0001c0001t0002g0294a0001c0001t0011g0218 | 2 | HG00741.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.373+1028_373+1029d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2798369 | |||||
| chrX:2798369
|
CT | C | 16 | a0001c0001t0001g0093a0001c0001t0001g0142a0001c0001t0003g0085others(13): Show | 16 | HG01070.hp2 HG01074.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.373+1029delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2798369 | |||||
| chrX:2798369
|
CTT | C | 31 | a0001c0001t0001g0032a0001c0001t0001g0107a0001c0001t0001g0139others(28): Show | 31 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.373+1028_373+1029d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2798369 | |||||
| chrX:2798373
|
T | C | 5 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0003g0236others(2): Show | 5 | HG01175.hp1 HG01361.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.373+1013T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2798373 | ||||||
| chrX:2798374
|
T | C | 1 | a0001c0001t0024g0088 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.373+1014T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2798374 | ||||||
| chrX:2798570
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.373+1210C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2798570 | ||||||
| chrX:2798756
|
T | TC | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+1397dupC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2798756 | |||||
| chrX:2798805
|
C | CT | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+1447dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2798805 | |||||
| chrX:2798818
|
C | CT | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+1463dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2798818 | |||||
| chrX:2798827
|
T | TA | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+1471dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2798827 | |||||
| chrX:2798872
|
T | TTTTTTC | 6 | a0001c0001t0005g0145a0001c0001t0007g0064a0001c0001t0021g0021others(3): Show | 6 | HG00741.hp1 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.373+1522_373+1527d others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2798872 | |||||
| chrX:2798885
|
T | TTTTTC | 29 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0139others(26): Show | 29 | HG01167.hp1 HG01169.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.373+1527_373+1528i others(7): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2798885 | |||||
| chrX:2798886
|
T | TTTTC | 3 | a0001c0001t0001g0107a0001c0002t0005g0275a0001c0002t0007g0308 | 3 | HG01168.hp2 HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.373+1527_373+1528i others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2798886 | |||||
| chrX:2798888
|
C | T | 38 | a0001c0001t0001g0032a0001c0001t0001g0093a0001c0001t0001g0107others(35): Show | 38 | HG00741.hp1 HG01167.hp1 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.373+1528C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2798888 | ||||||
| chrX:2798888
|
CT | C | 3 | a0001c0001t0001g0232a0001c0001t0004g0185a0001c0001t0023g0006 | 3 | HG01070.hp2 HG03491.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.373+1541delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2798888 | |||||
| chrX:2798925
|
G | A | 1 | a0001c0001t0009g0136 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.373+1565G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2798925 | ||||||
| chrX:2798992
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.373+1632A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2798992 | ||||||
| chrX:2799007
|
T | TA | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+1650dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2799007 | |||||
| chrX:2799026
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(156): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.373+1666T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2799026 | ||||||
| chrX:2799116
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.373+1756G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2799116 | ||||||
| chrX:2799193
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.373+1833C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2799193 | ||||||
| chrX:2799226
|
A | AC | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+1866_373+1867i others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2799226 | ||||||
| chrX:2799354
|
G | C | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.373+1994G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2799354 | ||||||
| chrX:2799497
|
A | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.373+2137A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2799497 | ||||||
| chrX:2799579
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.373+2219G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2799579 | ||||||
| chrX:2799616
|
C | CG | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+2261dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2799616 | |||||
| chrX:2799617
|
G | A | 3 | a0001c0001t0013g0303a0001c0001t0013g0307a0001c0001t0013g0309 | 3 | HG01884.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.373+2257G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2799617 | ||||||
| chrX:2799635
|
G | A | 4 | a0001c0001t0001g0304a0001c0001t0019g0188a0001c0001t0046g0123others(1): Show | 4 | HG02922.hp2 HG02976.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.373+2275G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2799635 | ||||||
| chrX:2799747
|
AC | A | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+2389delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2799747 | |||||
| chrX:2799770
|
T | TG | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+2411dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2799770 | |||||
| chrX:2799859
|
G | GT | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+2502dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2799859 | |||||
| chrX:2799910
|
T | TG | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+2551dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2799910 | |||||
| chrX:2799959
|
C | CA | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+2602dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2799959 | |||||
| chrX:2800025
|
T | C | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+2665T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800025 | ||||||
| chrX:2800028
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+2668C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800028 | ||||||
| chrX:2800030
|
T | A | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+2670T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800030 | ||||||
| chrX:2800094
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.373+2734T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800094 | ||||||
| chrX:2800114
|
A | G | 1 | a0001c0001t0002g0097 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.373+2754A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800114 | ||||||
| chrX:2800139
|
A | T | 1 | a0001c0001t0001g0115 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.373+2779A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800139 | ||||||
| chrX:2800295
|
GA | G | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+2936delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800295 | ||||||
| chrX:2800310
|
C | CA | 1 | a0001c0001t0016g0277 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.373+2951dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2800310 | |||||
| chrX:2800354
|
A | ATG | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+2994_373+2995i others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800354 | ||||||
| chrX:2800357
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+2997G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800357 | ||||||
| chrX:2800424
|
T | TG | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+3066dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2800424 | |||||
| chrX:2800558
|
T | C | 2 | a0001c0001t0019g0188a0001c0001t0046g0123 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.373+3198T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800558 | ||||||
| chrX:2800622
|
TC | T | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+3265delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2800622 | |||||
| chrX:2800652
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+3292G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800652 | ||||||
| chrX:2800653
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+3293A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800653 | ||||||
| chrX:2800688
|
C | CA | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+3330dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2800688 | |||||
| chrX:2800734
|
TC | T | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+3377delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2800734 | |||||
| chrX:2800796
|
TG | T | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+3439delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2800796 | |||||
| chrX:2800975
|
C | CA | 82 | a0001c0001t0001g0041a0001c0001t0001g0057a0001c0001t0001g0069others(79): Show | 82 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.373+3638dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2800975 | |||||
| chrX:2800975
|
C | CAA | 6 | a0001c0001t0003g0187a0001c0001t0003g0201a0001c0001t0019g0188others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.373+3637_373+3638d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2800975 | |||||
| chrX:2800975
|
CA | C | 25 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0228others(22): Show | 25 | HG00733.hp1 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.373+3638delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2800975 | |||||
| chrX:2800975
|
CAA | C | 2 | a0001c0001t0001g0142a0001c0001t0025g0317 | 2 | HG03471.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.373+3637_373+3638d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2800975 | |||||
| chrX:2800975
|
CAAAAAAA others(1): Show |
C | 1 | a0001c0007t0032g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.373+3631_373+3638d others(10): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2800975 | |||||
| chrX:2801070
|
G | T | 107 | a0001c0001t0001g0041a0001c0001t0001g0057a0001c0001t0001g0069others(104): Show | 107 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.373+3710G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801070 | ||||||
| chrX:2801108
|
A | AAGGG | 1 | a0001c0001t0004g0195 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.373+3748_373+3749i others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801108 | ||||||
| chrX:2801109
|
G | A | 1 | a0001c0001t0004g0195 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.373+3749G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801109 | ||||||
| chrX:2801111
|
C | T | 1 | a0001c0001t0004g0195 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.373+3751C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801111 | ||||||
| chrX:2801113
|
T | G | 1 | a0001c0001t0004g0195 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.373+3753T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801113 | ||||||
| chrX:2801114
|
G | C | 1 | a0001c0001t0004g0195 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.373+3754G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801114 | ||||||
| chrX:2801116
|
T | A | 1 | a0001c0001t0004g0195 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.373+3756T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801116 | ||||||
| chrX:2801117
|
T | TAGAGAA | 1 | a0001c0001t0004g0195 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.373+3757_373+3758i others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801117 | ||||||
| chrX:2801150
|
T | G | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+3790T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801150 | ||||||
| chrX:2801201
|
CTG | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.373+3842_373+3843d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801201 | ||||||
| chrX:2801257
|
A | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(114): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.373+3897A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801257 | ||||||
| chrX:2801334
|
A | AG | 8 | a0001c0001t0003g0283a0001c0001t0007g0064a0001c0001t0008g0302others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.373+3977dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2801334 | |||||
| chrX:2801341
|
GAGAGAA | G | 3 | a0001c0001t0025g0317a0001c0001t0027g0026a0001c0001t0042g0133 | 3 | HG02280.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.373+3987_373+3992d others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2801341 | |||||
| chrX:2801447
|
G | A | 1 | a0001c0007t0032g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.373+4087G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801447 | ||||||
| chrX:2801625
|
G | A | 32 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0037others(29): Show | 32 | HG00621.hp1 HG01175.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.373+4265G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801625 | ||||||
| chrX:2801717
|
A | AT | 20 | a0001c0001t0001g0142a0001c0001t0003g0187a0001c0001t0005g0020others(17): Show | 20 | HG01070.hp2 HG01071.hp1 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.373+4366dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2801717 | |||||
| chrX:2801731
|
C | T | 19 | a0001c0001t0001g0142a0001c0001t0005g0020a0001c0001t0005g0046others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.373+4371C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801731 | ||||||
| chrX:2801739
|
C | G | 129 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(126): Show | 130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.373+4379C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801739 | ||||||
| chrX:2801747
|
C | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0139a0001c0001t0001g0143others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.373+4387C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801747 | ||||||
| chrX:2801747
|
C | T | 5 | a0001c0001t0005g0020a0001c0001t0005g0046a0001c0002t0005g0034others(2): Show | 5 | HG02109.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.373+4387C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801747 | ||||||
| chrX:2801762
|
G | A | 9 | a0001c0001t0005g0020a0001c0001t0005g0046a0001c0001t0023g0005others(6): Show | 9 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.373+4402G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801762 | ||||||
| chrX:2801763
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.373+4403C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801763 | ||||||
| chrX:2801769
|
C | T | 2 | a0001c0001t0001g0139a0001c0001t0001g0225 | 2 | HG00323.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.373+4409C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801769 | ||||||
| chrX:2801771
|
T | C | 20 | a0001c0001t0001g0142a0001c0001t0005g0020a0001c0001t0005g0046others(17): Show | 20 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.373+4411T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801771 | ||||||
| chrX:2801772
|
C | G | 21 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0005g0020others(18): Show | 21 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.373+4412C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801772 | ||||||
| chrX:2801799
|
C | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(122): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.373+4439C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801799 | ||||||
| chrX:2801810
|
G | A | 1 | a0001c0001t0005g0271 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.373+4450G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801810 | ||||||
| chrX:2801814
|
T | C | 1 | a0001c0001t0014g0096 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.373+4454T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801814 | ||||||
| chrX:2801841
|
T | TG | 1 | a0001c0005t0015g0045 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.373+4484dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2801841 | |||||
| chrX:2801854
|
G | A | 9 | a0001c0001t0001g0071a0001c0001t0001g0074a0001c0001t0001g0086others(6): Show | 9 | HG00438.hp1 HG00738.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.373+4494G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801854 | ||||||
| chrX:2801856
|
C | A | 2 | a0001c0001t0001g0093a0001c0001t0036g0002 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.373+4496C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801856 | ||||||
| chrX:2801898
|
G | A | 1 | a0001c0001t0002g0084 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.373+4538G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801898 | ||||||
| chrX:2801918
|
A | G | 79 | a0001c0001t0001g0041a0001c0001t0001g0057a0001c0001t0001g0069others(76): Show | 79 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.373+4558A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801918 | ||||||
| chrX:2801924
|
A | G | 1 | a0004c0009t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.373+4564A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801924 | ||||||
| chrX:2801929
|
G | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(117): Show | 121 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.373+4569G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801929 | ||||||
| chrX:2801950
|
G | A | 6 | a0001c0001t0013g0303a0001c0001t0013g0307a0001c0001t0013g0309others(3): Show | 6 | HG01884.hp1 HG02280.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.373+4590G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801950 | ||||||
| chrX:2801955
|
C | T | 6 | a0001c0001t0013g0303a0001c0001t0013g0307a0001c0001t0013g0309others(3): Show | 6 | HG01884.hp1 HG02280.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.373+4595C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801955 | ||||||
| chrX:2801977
|
G | A | 2 | a0002c0003t0040g0310a0002c0003t0045g0311 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.373+4617G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801977 | ||||||
| chrX:2801986
|
C | G | 35 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0037others(32): Show | 35 | HG00621.hp1 HG01175.hp1 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.373+4626C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801986 | ||||||
| chrX:2801998
|
C | T | 1 | a0001c0001t0026g0210 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.373+4638C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801998 | ||||||
| chrX:2802173
|
T | G | 1 | a0001c0001t0002g0097 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.374-4528T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2802173 | ||||||
| chrX:2802321
|
AT | A | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.374-4375delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2802321 | |||||
| chrX:2802543
|
C | T | 4 | a0001c0001t0003g0283a0002c0003t0040g0310a0002c0003t0045g0311others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.374-4158C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2802543 | ||||||
| chrX:2802661
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(116): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.374-4040A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2802661 | ||||||
| chrX:2802845
|
A | C | 2 | a0001c0001t0001g0244a0001c0001t0001g0315 | 2 | HG00733.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.374-3856A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2802845 | ||||||
| chrX:2803216
|
A | G | 22 | a0001c0001t0001g0304a0001c0001t0005g0020a0001c0001t0005g0046others(19): Show | 22 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.374-3485A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803216 | ||||||
| chrX:2803276
|
C | T | 2 | a0001c0001t0019g0188a0001c0001t0046g0123 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.374-3425C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803276 | ||||||
| chrX:2803302
|
C | G | 7 | a0001c0001t0001g0304a0001c0001t0013g0303a0001c0001t0013g0307others(4): Show | 7 | HG01884.hp1 HG02280.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.374-3399C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803302 | ||||||
| chrX:2803372
|
G | A | 1 | a0001c0001t0025g0027 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.374-3329G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803372 | ||||||
| chrX:2803543
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.374-3158G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803543 | ||||||
| chrX:2803599
|
AG | A | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.374-3096delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2803599 | |||||
| chrX:2803601
|
G | A | 20 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0005g0020others(17): Show | 20 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.374-3100G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803601 | ||||||
| chrX:2803605
|
G | T | 129 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(126): Show | 130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.374-3096G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803605 | ||||||
| chrX:2803747
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(138): Show | 142 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.374-2954A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803747 | ||||||
| chrX:2803852
|
GT | G | 1 | a0001c0001t0001g0224 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.374-2842delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2803852 | |||||
| chrX:2803921
|
C | A | 5 | a0001c0001t0010g0193a0001c0001t0020g0131a0001c0001t0020g0138others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.374-2780C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803921 | ||||||
| chrX:2803937
|
G | C | 79 | a0001c0001t0001g0041a0001c0001t0001g0057a0001c0001t0001g0069others(76): Show | 79 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.374-2764G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803937 | ||||||
| chrX:2803983
|
C | T | 2 | a0001c0001t0013g0303a0001c0001t0013g0307 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.374-2718C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803983 | ||||||
| chrX:2804015
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(151): Show | 155 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.374-2686A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804015 | ||||||
| chrX:2804134
|
C | A | 1 | a0001c0001t0001g0205 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.374-2567C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804134 | ||||||
| chrX:2804173
|
T | G | 20 | a0001c0001t0001g0304a0001c0001t0005g0020a0001c0001t0005g0046others(17): Show | 20 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.374-2528T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804173 | ||||||
| chrX:2804195
|
A | T | 1 | a0001c0001t0002g0262 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.374-2506A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804195 | ||||||
| chrX:2804474
|
A | G | 3 | a0001c0001t0001g0169a0001c0001t0006g0080a0001c0001t0028g0279 | 3 | HG00438.hp2 NA18959.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.374-2227A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804474 | ||||||
| chrX:2804548
|
C | T | 1 | a0001c0002t0008g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.374-2153C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804548 | ||||||
| chrX:2804557
|
C | T | 1 | a0004c0009t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.374-2144C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804557 | ||||||
| chrX:2804697
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0036g0002 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.374-2004G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804697 | ||||||
| chrX:2804813
|
G | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0252a0001c0001t0004g0068 | 3 | HG01123.hp2 HG02273.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.374-1888G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804813 | ||||||
| chrX:2804842
|
A | G | 3 | a0001c0001t0001g0183a0001c0001t0001g0252a0001c0001t0004g0068 | 3 | HG01123.hp2 HG02273.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.374-1859A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804842 | ||||||
| chrX:2804846
|
A | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0252a0001c0001t0004g0068 | 3 | HG01123.hp2 HG02273.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.374-1855A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804846 | ||||||
| chrX:2804854
|
G | A | 3 | a0001c0001t0001g0183a0001c0001t0001g0252a0001c0001t0004g0068 | 3 | HG01123.hp2 HG02273.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.374-1847G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804854 | ||||||
| chrX:2804965
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.374-1736C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804965 | ||||||
| chrX:2805203
|
G | A | 2 | a0001c0001t0021g0021a0001c0001t0021g0278 | 2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.374-1498G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2805203 | ||||||
| chrX:2805259
|
C | T | 1 | a0001c0001t0011g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.374-1442C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2805259 | ||||||
| chrX:2805262
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.374-1439C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2805262 | ||||||
| chrX:2805509
|
C | T | 20 | a0001c0001t0001g0304a0001c0001t0003g0047a0001c0001t0003g0048others(17): Show | 20 | HG00408.hp2 HG00741.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.374-1192C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2805509 | ||||||
| chrX:2805610
|
C | T | 6 | a0001c0001t0001g0209a0001c0001t0001g0249a0001c0001t0001g0264others(3): Show | 6 | HG01433.hp2 HG02004.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.374-1091C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2805610 | ||||||
| chrX:2805625
|
C | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(110): Show | 114 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.374-1076C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2805625 | ||||||
| chrX:2805634
|
A | G | 9 | a0001c0001t0012g0289a0002c0003t0001g0028a0002c0003t0001g0141others(6): Show | 9 | HG00741.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.374-1067A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2805634 | ||||||
| chrX:2805674
|
T | G | 65 | a0001c0001t0001g0070a0001c0001t0001g0114a0001c0001t0001g0157others(62): Show | 65 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.374-1027T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2805674 | ||||||
| chrX:2805835
|
A | G | 6 | a0001c0001t0001g0056a0001c0001t0001g0090a0001c0001t0001g0296others(3): Show | 6 | HG02074.hp1 HG02129.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.374-866A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2805835 | ||||||
| chrX:2805959
|
TA | T | 1 | a0001c0001t0001g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.374-741delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2805959 | ||||||
| chrX:2806120
|
T | C | 1 | a0001c0002t0005g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.374-581T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2806120 | ||||||
| chrX:2806126
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.374-575C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2806126 | ||||||
| chrX:2806130
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.374-571C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2806130 | ||||||
| chrX:2806198
|
A | AT | 3 | a0001c0001t0001g0104a0001c0001t0001g0280a0001c0001t0004g0146 | 3 | HG02523.hp1 NA18946.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.374-491dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2806198 | |||||
| chrX:2806198
|
AT | A | 2 | a0001c0001t0004g0185a0001c0001t0030g0091 | 2 | NA19054.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.374-491delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2806198 | |||||
| chrX:2806220
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.374-481C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2806220 | ||||||
| chrX:2806339
|
CT | C | 1 | a0002c0003t0045g0311 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.374-353delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2806339 | |||||
| chrX:2806348
|
T | A | 65 | a0001c0001t0001g0070a0001c0001t0001g0114a0001c0001t0001g0157others(62): Show | 65 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.374-353T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2806348 | ||||||
| chrX:2806349
|
A | T | 1 | a0001c0001t0001g0074 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.374-352A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2806349 | ||||||
| chrX:2806388
|
A | C | 62 | a0001c0001t0001g0070a0001c0001t0001g0114a0001c0001t0001g0157others(59): Show | 62 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.374-313A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2806388 | ||||||
| chrX:2806398
|
CT | C | 6 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0061others(3): Show | 6 | HG02055.hp1 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.374-294delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2806398 | |||||
| chrX:2806407
|
T | A | 62 | a0001c0001t0001g0070a0001c0001t0001g0114a0001c0001t0001g0157others(59): Show | 62 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.374-294T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2806407 | ||||||
| chrX:2806505
|
C | A | 1 | a0002c0003t0008g0066 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.374-196C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2806505 | ||||||
| chrX:2806995
|
C | CAT | 165 | a0001c0001t0001g0041a0001c0001t0001g0069a0001c0001t0001g0070others(162): Show | 165 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.418+250_418+251ins others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2806995 | ||||||
| chrX:2806996
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.418+251G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2806996 | ||||||
| chrX:2807006
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.418+261A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807006 | ||||||
| chrX:2807009
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.418+264C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807009 | ||||||
| chrX:2807011
|
T | C | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.418+266T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807011 | ||||||
| chrX:2807051
|
G | A | 6 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0061others(3): Show | 6 | HG02055.hp1 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.418+306G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807051 | ||||||
| chrX:2807133
|
C | CTG | 302 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.418+391_418+392dup others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2807133 | |||||
| chrX:2807258
|
A | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(282): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.418+513A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807258 | ||||||
| chrX:2807430
|
GCACA | G | 1 | a0001c0001t0010g0050 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.418+694_418+697del others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2807430 | |||||
| chrX:2807477
|
T | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(282): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.419-708T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807477 | ||||||
| chrX:2807502
|
A | T | 285 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(282): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.419-683A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807502 | ||||||
| chrX:2807504
|
ACATGTGC others(15): Show |
A | 284 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(281): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.419-667_419-646del others(22): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2807504 | |||||
| chrX:2807619
|
T | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.419-566T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807619 | ||||||
| chrX:2807743
|
G | A | 1 | a0001c0002t0012g0049 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.419-442G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807743 | ||||||
| chrX:2807750
|
T | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(280): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.419-435T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807750 | ||||||
| chrX:2807842
|
T | C | 301 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(298): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.419-343T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807842 | ||||||
| chrX:2807906
|
T | C | 5 | a0001c0001t0005g0003a0001c0001t0005g0029a0001c0001t0005g0030others(2): Show | 5 | HG01261.hp1 HG02280.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.419-279T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807906 | ||||||
| chrX:2808104
|
C | T | 1 | a0001c0001t0004g0185 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.419-81C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2808104 | ||||||
| chrX:2808329
|
G | A | 9 | a0001c0001t0001g0196a0001c0001t0004g0111a0001c0001t0004g0126others(6): Show | 9 | NA18948.hp1 NA18952.hp1 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.454+109G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2808329 | ||||||
| chrX:2808355
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.454+135A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2808355 | ||||||
| chrX:2808606
|
T | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.454+386T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2808606 | ||||||
| chrX:2808745
|
C | T | 1 | a0001c0001t0003g0250 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.454+525C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2808745 | ||||||
| chrX:2808772
|
C | T | 1 | a0001c0002t0005g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.454+552C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2808772 | ||||||
| chrX:2809114
|
TC | T | 2 | a0001c0001t0014g0207a0001c0001t0017g0044 | 2 | HG00558.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.454+899delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2809114 | |||||
| chrX:2809210
|
G | T | 1 | a0001c0001t0001g0142 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.454+990G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2809210 | ||||||
| chrX:2809323
|
TG | T | 1 | a0002c0003t0045g0311 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.454+1106delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2809323 | |||||
| chrX:2809457
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.454+1237C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2809457 | ||||||
| chrX:2809556
|
AT | A | 2 | a0001c0001t0005g0305a0001c0001t0005g0306 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.454+1337delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2809556 | ||||||
| chrX:2809582
|
C | CA | 1 | a0001c0002t0005g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.454+1368dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2809582 | |||||
| chrX:2809632
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0003g0063 | 2 | HG02698.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.454+1412C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2809632 | ||||||
| chrX:2809689
|
CT | C | 1 | a0001c0001t0030g0091 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.454+1471delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2809689 | |||||
| chrX:2809757
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.454+1537G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2809757 | ||||||
| chrX:2809794
|
C | T | 1 | a0001c0001t0009g0031 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.455-1542C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2809794 | ||||||
| chrX:2809893
|
T | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.455-1443T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2809893 | ||||||
| chrX:2810023
|
C | T | 1 | a0004c0009t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.455-1313C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810023 | ||||||
| chrX:2810129
|
TC | T | 1 | a0001c0001t0030g0091 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.455-1201delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2810129 | |||||
| chrX:2810180
|
A | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(287): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.455-1156A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810180 | ||||||
| chrX:2810218
|
C | G | 1 | a0001c0001t0003g0215 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.455-1118C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810218 | ||||||
| chrX:2810475
|
T | C | 91 | a0001c0001t0001g0041a0001c0001t0001g0069a0001c0001t0001g0083others(88): Show | 91 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.455-861T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810475 | ||||||
| chrX:2810520
|
T | C | 12 | a0001c0001t0002g0174a0001c0001t0006g0025a0001c0001t0006g0060others(9): Show | 12 | HG00438.hp2 HG02080.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.455-816T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810520 | ||||||
| chrX:2810777
|
A | G | 3 | a0001c0001t0001g0139a0001c0005t0015g0045a0001c0005t0015g0051 | 3 | HG02809.hp2 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.455-559A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810777 | ||||||
| chrX:2810831
|
G | A | 94 | a0001c0001t0001g0041a0001c0001t0001g0069a0001c0001t0001g0083others(91): Show | 94 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.455-505G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810831 | ||||||
| chrX:2810850
|
A | AGTCCCG | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-485_455-484ins others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2810850 | |||||
| chrX:2810855
|
G | T | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-481G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810855 | ||||||
| chrX:2810856
|
C | CA | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-479dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2810856 | |||||
| chrX:2810859
|
T | C | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-477T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810859 | ||||||
| chrX:2810861
|
A | ATTCTCCT others(1): Show |
1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-475_455-474ins others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810861 | ||||||
| chrX:2810862
|
A | C | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-474A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810862 | ||||||
| chrX:2810865
|
G | C | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-471G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810865 | ||||||
| chrX:2810868
|
A | C | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-468A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810868 | ||||||
| chrX:2810871
|
A | C | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-465A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810871 | ||||||
| chrX:2810872
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.455-464C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810872 | ||||||
| chrX:2810873
|
GCCACTGT | G | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-462_455-456del others(7): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810873 | ||||||
| chrX:2810882
|
T | A | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-454T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810882 | ||||||
| chrX:2810902
|
CA | C | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-432delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2810902 | |||||
| chrX:2810908
|
TC | T | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-426delC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2810908 | |||||
| chrX:2810911
|
G | A | 2 | a0001c0005t0015g0045a0001c0005t0015g0051 | 2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.455-425G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810911 | ||||||
| chrX:2810912
|
T | G | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-424T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810912 | ||||||
| chrX:2810918
|
AAAATAAT | A | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-415_455-409del others(7): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2810918 | |||||
| chrX:2810925
|
TAAGA | T | 4 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0005t0015g0045others(1): Show | 4 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-408_455-405del others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2810925 | |||||
| chrX:2810926
|
A | T | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-410A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810926 | ||||||
| chrX:2810928
|
G | GAAAT | 1 | a0001c0001t0006g0077 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.455-384_455-381dup others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2810928 | |||||
| chrX:2810928
|
GAAAT | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(120): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.455-384_455-381del others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2810928 | |||||
| chrX:2810928
|
GAAATAAA others(1): Show |
G | 94 | a0001c0001t0001g0041a0001c0001t0001g0069a0001c0001t0001g0083others(91): Show | 94 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.455-388_455-381del others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2810928 | |||||
| chrX:2810930
|
A | T | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-406A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810930 | ||||||
| chrX:2810931
|
AT | A | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-404delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810931 | ||||||
| chrX:2810940
|
T | G | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-396T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810940 | ||||||
| chrX:2810952
|
TA | T | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-380delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2810952 | |||||
| chrX:2810965
|
A | G | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-371A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810965 | ||||||
| chrX:2810970
|
A | T | 96 | a0001c0001t0001g0041a0001c0001t0001g0069a0001c0001t0001g0083others(93): Show | 96 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.455-366A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810970 | ||||||
| chrX:2811105
|
G | GT | 1 | a0001c0001t0002g0132 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.455-222dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2811105 | |||||
| chrX:2811115
|
CT | C | 172 | a0001c0001t0001g0041a0001c0001t0001g0069a0001c0001t0001g0070others(169): Show | 172 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.455-212delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2811115 | |||||
| chrX:2811172
|
C | G | 2 | a0001c0001t0004g0126a0001c0001t0004g0127 | 2 | NA18961.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.455-164C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2811172 | ||||||
| chrX:2811240
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(119): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.455-96A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2811240 | ||||||
| chrX:2811243
|
C | T | 2 | a0001c0005t0015g0045a0001c0005t0015g0051 | 2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.455-93C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2811243 | ||||||
| chrX:2811305
|
G | A | 102 | a0001c0001t0001g0041a0001c0001t0001g0069a0001c0001t0001g0083others(99): Show | 102 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.455-31G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2811305 | ||||||
| chrX:2811495
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.571+43G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2811495 | ||||||
| chrX:2811498
|
T | TC | 1 | a0001c0002t0005g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.571+46_571+47insC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2811498 | ||||||
| chrX:2811499
|
T | A | 1 | a0001c0002t0005g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.571+47T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2811499 | ||||||
| chrX:2811499
|
T | TA | 209 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(206): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.571+58dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2811499 | |||||
| chrX:2811499
|
T | TAA | 4 | a0001c0001t0001g0304a0001c0001t0002g0067a0001c0001t0002g0181others(1): Show | 4 | HG01123.hp1 HG01981.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.571+57_571+58dupAA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2811499 | |||||
| chrX:2811706
|
T | C | 2 | a0001c0001t0021g0021a0001c0001t0021g0278 | 2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.571+254T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2811706 | ||||||
| chrX:2811721
|
G | A | 1 | a0001c0001t0004g0111 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.571+269G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2811721 | ||||||
| chrX:2811820
|
T | C | 1 | a0001c0001t0025g0027 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.571+368T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2811820 | ||||||
| chrX:2811880
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.571+428G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2811880 | ||||||
| chrX:2811893
|
G | GCCAA | 1 | a0001c0001t0002g0132 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.571+443_571+446dup others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2811893 | |||||
| chrX:2812017
|
C | G | 2 | a0001c0001t0003g0012a0001c0001t0030g0091 | 2 | NA18980.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.571+565C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2812017 | ||||||
| chrX:2812078
|
A | AGCCAAAT others(5): Show |
137 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(134): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.571+626_571+627ins others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2812078 | ||||||
| chrX:2812079
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(134): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.571+627C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2812079 | ||||||
| chrX:2812232
|
C | T | 1 | a0001c0001t0010g0050 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.571+780C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2812232 | ||||||
| chrX:2812248
|
G | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(120): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.571+796G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2812248 | ||||||
| chrX:2812568
|
C | CA | 1 | a0001c0001t0030g0091 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.571+1121dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2812568 | |||||
| chrX:2812675
|
C | G | 2 | a0001c0001t0001g0105a0001c0001t0039g0036 | 2 | NA18946.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.571+1223C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2812675 | ||||||
| chrX:2812790
|
C | T | 1 | a0004c0009t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.571+1338C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2812790 | ||||||
| chrX:2813390
|
C | CA | 1 | a0001c0001t0030g0091 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.572-971dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2813390 | |||||
| chrX:2813498
|
G | C | 1 | a0001c0001t0004g0111 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.572-866G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2813498 | ||||||
| chrX:2813519
|
C | G | 1 | a0002c0008t0037g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.572-845C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2813519 | ||||||
| chrX:2813565
|
TG | T | 1 | a0001c0001t0030g0091 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.572-797delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2813565 | |||||
| chrX:2813720
|
T | C | 63 | a0001c0001t0001g0134a0001c0001t0001g0175a0001c0001t0002g0067others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.572-644T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2813720 | ||||||
| chrX:2813764
|
T | C | 1 | a0002c0003t0007g0009 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.572-600T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2813764 | ||||||
| chrX:2813788
|
A | G | 2 | a0001c0001t0025g0027a0001c0001t0025g0317 | 2 | HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.572-576A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2813788 | ||||||
| chrX:2813817
|
T | TA | 1 | a0002c0003t0045g0311 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.572-545dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2813817 | |||||
| chrX:2813864
|
TA | T | 1 | a0001c0001t0030g0091 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.572-498delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2813864 | |||||
| chrX:2813943
|
AT | A | 1 | a0001c0001t0030g0091 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.572-417delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2813943 | |||||
| chrX:2814055
|
C | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.572-309C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2814055 | ||||||
| chrX:2814116
|
C | CT | 1 | a0001c0001t0030g0091 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.572-240dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2814116 | |||||
| chrX:2814125
|
A | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.572-239A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2814125 | ||||||
| chrX:2814166
|
A | G | 27 | a0001c0001t0001g0287a0001c0001t0001g0312a0001c0001t0003g0047others(24): Show | 27 | HG00408.hp2 HG00544.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.572-198A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2814166 | ||||||
| chrX:2814315
|
C | CT | 233 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(230): Show | 234 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.572-39dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2814315 | |||||
| chrX:2814315
|
C | CTT | 71 | a0001c0001t0001g0134a0001c0001t0001g0175a0001c0001t0002g0067others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.572-40_572-39dupTT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2814315 | |||||
| chrX:2814315
|
C | CTTT | 3 | a0001c0001t0001g0304a0001c0001t0025g0027a0001c0001t0025g0317 | 3 | HG03225.hp2 HG03453.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.572-41_572-39dupTT others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2814315 |