Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4810 |
|---|---|
| ensemblid | ENSG00000188158.17 |
| hgncid | 7820 |
| symbol | NHS |
| name | NHS actin remodeling regulator |
| refseq_nuc | NM_001291867.2 |
| refseq_prot | NP_001278796.1 |
| ensembl_nuc | ENST00000676302.1 |
| ensembl_prot | ENSP00000502262.1 |
| mane_status | MANE Select |
| chr | chrX |
| start | 17375200 |
| end | 17735994 |
| strand | + |
| ver | v1.2 |
| region | chrX:17375200-17735994 |
| region5000 | chrX:17370200-17740994 |
| regionname0 | NHS_chrX_17375200_17735994 |
| regionname5000 | NHS_chrX_17370200_17740994 |
| 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 | 1651 | 73 | 28 | 12 | 32 | 0 | 1 | 25 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0002 | 0/0 | 1651 | 66 | 4 | 13 | 30 | 5 | 14 | 20 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0003 | 0/0 | 1651 | 5 | 0 | 2 | 3 | 0 | 0 | 3 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0004 | 0/0 | 1651 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0005 | 0/0 | 1650 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0006 | 0/0 | 1651 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0007 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0008 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0009 | 0/0 | 1651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0010 | 0/0 | 1651 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0011 | 0/0 | 1651 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0012 | 0/0 | 1651 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0013 | 0/0 | 1639 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| 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 | 4956 | 68 | 24 | 11 | 32 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| c0002 | 0/0 | 4956 | 65 | 4 | 13 | 30 | 4 | 14 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| c0003 | 0/0 | 4956 | 5 | 4 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| c0004 | 0/0 | 4956 | 5 | 0 | 2 | 3 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| c0005 | 0/0 | 4956 | 5 | 5 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| c0006 | 0/0 | 4953 | 4 | 3 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| c0007 | 0/0 | 4956 | 2 | 2 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| c0008 | 0/0 | 4956 | 2 | 2 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| c0009 | 0/0 | 4953 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| c0010 | 0/0 | 4953 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| c0011 | 0/0 | 4956 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| c0012 | 0/0 | 4956 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| c0013 | 0/0 | 4956 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| c0014 | 0/0 | 4956 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| c0015 | 0/0 | 4956 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| c0016 | 0/0 | 4920 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| 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 | 4089 | 109 | 11 | 20 | 59 | 5 | 14 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| t0002 | 0/0 | 4089 | 27 | 21 | 6 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| t0003 | 0/0 | 4089 | 5 | 4 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| t0004 | 0/0 | 4089 | 3 | 0 | 1 | 2 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| t0005 | 0/0 | 4094 | 3 | 3 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| t0006 | 0/0 | 4090 | 2 | 1 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| t0007 | 0/0 | 4089 | 2 | 0 | 0 | 2 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| t0008 | 0/0 | 4088 | 2 | 2 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| t0009 | 0/0 | 4089 | 2 | 2 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| t0010 | 0/0 | 4089 | 2 | 2 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| t0011 | 0/0 | 4089 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| t0012 | 0/0 | 4090 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| t0013 | 0/0 | 4089 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| t0014 | 0/0 | 4088 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| t0015 | 0/0 | 4102 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| t0016 | 0/0 | 4087 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| t0017 | 0/0 | 4089 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| 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 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| 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 | 4956 | 68 | 24 | 11 | 32 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0001c0003 | 0/0 | 4956 | 5 | 4 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0002c0002 | 0/0 | 4956 | 65 | 4 | 13 | 30 | 4 | 14 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0002c0015 | 0/0 | 4956 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0003c0004 | 0/0 | 4956 | 5 | 0 | 2 | 3 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0004c0005 | 0/0 | 4956 | 5 | 5 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0005c0006 | 0/0 | 4953 | 4 | 3 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0006c0007 | 0/0 | 4956 | 2 | 2 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0006c0008 | 0/0 | 4956 | 2 | 2 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0007c0009 | 0/0 | 4953 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0008c0010 | 0/0 | 4953 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0009c0011 | 0/0 | 4956 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0010c0012 | 0/0 | 4956 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0011c0013 | 0/0 | 4956 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0012c0014 | 0/0 | 4956 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0013c0016 | 0/0 | 4920 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9044 | 37 | 6 | 4 | 26 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0001c0001t0002 | 0/0 | 9044 | 17 | 12 | 5 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0001c0001t0004 | 0/0 | 9044 | 3 | 0 | 1 | 2 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0001c0001t0005 | 0/0 | 9049 | 2 | 2 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0001c0001t0006 | 0/0 | 9045 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0001c0001t0007 | 0/0 | 9044 | 2 | 0 | 0 | 2 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0001c0001t0009 | 0/0 | 9044 | 2 | 2 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0001c0001t0012 | 0/0 | 9045 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0001c0001t0013 | 0/0 | 9044 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0001c0001t0015 | 0/0 | 9057 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0001c0001t0017 | 0/0 | 9044 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0001c0003t0002 | 0/0 | 9044 | 5 | 4 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0002c0002t0001 | 0/0 | 9044 | 61 | 3 | 13 | 28 | 4 | 13 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0002c0002t0006 | 0/0 | 9045 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0002c0002t0011 | 0/0 | 9044 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0002c0002t0014 | 0/0 | 9043 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0002c0002t0016 | 0/0 | 9042 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0002c0015t0001 | 0/0 | 9044 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0003c0004t0001 | 0/0 | 9044 | 5 | 0 | 2 | 3 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0004c0005t0003 | 0/0 | 9044 | 3 | 3 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0004c0005t0010 | 0/0 | 9044 | 2 | 2 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0005c0006t0001 | 0/0 | 9041 | 2 | 1 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0005c0006t0005 | 0/0 | 9046 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0005c0006t0008 | 0/0 | 9040 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0006c0007t0002 | 0/0 | 9044 | 2 | 2 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0006c0008t0001 | 0/0 | 9044 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0006c0008t0008 | 0/0 | 9043 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0007c0009t0002 | 0/0 | 9041 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0008c0010t0003 | 0/0 | 9041 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0009c0011t0002 | 0/0 | 9044 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0010c0012t0001 | 0/0 | 9044 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0011c0013t0001 | 0/0 | 9044 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0012c0014t0003 | 0/0 | 9044 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| a0013c0016t0002 | 0/0 | 9008 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | copy fasta | chrX | 17370200 | 17740994 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0007g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0009g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0009g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0012g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0013g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0015g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0017g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0003t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0003t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0003t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0003t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0003t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0006g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0011g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0014g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0016g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0015t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0003c0004t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0003c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0003c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0003c0004t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0003c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0004c0005t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0004c0005t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0004c0005t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0004c0005t0010g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0004c0005t0010g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0005c0006t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0005c0006t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0005c0006t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0005c0006t0008g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0006c0007t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0006c0007t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0006c0008t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0006c0008t0008g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0007c0009t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0008c0010t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0009c0011t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0010c0012t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0011c0013t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0012c0014t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0013c0016t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0045 | EUR | GBR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0021 | EUR | FIN | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | CHS | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00621 | hp1 | a0002 | c0002 | t0016 | g0005 | EAS | CHS | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0123 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0152 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | CHS | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0130 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01071 | hp2 | a0012 | c0014 | t0003 | g0092 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0032 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01106 | hp1 | a0005 | c0006 | t0001 | g0157 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0040 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0033 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0028 | AMR | CLM | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01258 | hp1 | a0001 | c0003 | t0002 | g0019 | AMR | CLM | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0163 | AMR | CLM | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0074 | AMR | CLM | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | CLM | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0008 | EUR | IBS | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | PEL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01952 | hp1 | a0003 | c0004 | t0001 | g0132 | AMR | PEL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01975 | hp1 | a0001 | c0001 | t0017 | g0154 | AMR | PEL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0030 | AMR | PEL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02055 | hp1 | a0004 | c0005 | t0003 | g0100 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02145 | hp1 | a0006 | c0008 | t0008 | g0113 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02257 | hp1 | a0002 | c0002 | t0011 | g0020 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02257 | hp2 | a0009 | c0011 | t0002 | g0147 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02280 | hp2 | a0001 | c0003 | t0002 | g0128 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0077 | AMR | PEL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02300 | hp1 | a0003 | c0004 | t0001 | g0013 | AMR | PEL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02572 | hp1 | a0001 | c0003 | t0002 | g0142 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0131 | SAS | PJL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02615 | hp1 | a0006 | c0007 | t0002 | g0118 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0122 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02622 | hp2 | a0005 | c0006 | t0005 | g0159 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02630 | hp2 | a0013 | c0016 | t0002 | g0119 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02647 | hp1 | a0004 | c0005 | t0003 | g0136 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02723 | hp2 | a0008 | c0010 | t0003 | g0158 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0034 | SAS | PJL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0082 | SAS | PJL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02809 | hp2 | a0006 | c0007 | t0002 | g0115 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02922 | hp1 | a0005 | c0006 | t0001 | g0162 | AFR | ESN | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02922 | hp2 | a0001 | c0003 | t0002 | g0101 | AFR | ESN | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02965 | hp1 | a0004 | c0005 | t0010 | g0086 | AFR | ESN | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0072 | SAS | PJL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03041 | hp1 | a0006 | c0008 | t0001 | g0114 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0155 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | MSL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | MSL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0103 | AFR | MSL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03453 | hp2 | a0007 | c0009 | t0002 | g0160 | AFR | MSL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0064 | SAS | PJL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03516 | hp1 | a0004 | c0005 | t0003 | g0117 | AFR | ESN | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0125 | AFR | ESN | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | MSL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0076 | SAS | PJL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0109 | SAS | STU | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0141 | SAS | BEB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0035 | SAS | STU | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG04199 | hp1 | a0002 | c0002 | t0014 | g0063 | SAS | STU | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0078 | SAS | STU | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0075 | SAS | STU | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | CHB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0111 | AFR | YRI | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | YRI | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18948 | hp1 | a0010 | c0012 | t0001 | g0150 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18952 | hp1 | a0001 | c0001 | t0015 | g0079 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18965 | hp1 | a0001 | c0001 | t0013 | g0059 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18977 | hp1 | a0011 | c0013 | t0001 | g0039 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18990 | hp1 | a0003 | c0004 | t0001 | g0149 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19000 | hp1 | a0002 | c0002 | t0006 | g0060 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19007 | hp1 | a0003 | c0004 | t0001 | g0055 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0112 | AFR | LWK | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19030 | hp2 | a0001 | c0001 | t0012 | g0044 | AFR | LWK | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | LWK | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19068 | hp1 | a0003 | c0004 | t0001 | g0066 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19076 | hp1 | a0001 | c0001 | t0007 | g0102 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA20752 | hp1 | a0002 | c0015 | t0001 | g0046 | EUR | TSI | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0017 | EUR | TSI | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0080 | SAS | GIH | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02486 | hp1 | a0004 | c0005 | t0010 | g0097 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03471 | hp1 | a0005 | c0006 | t0008 | g0161 | AFR | MSL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | USA | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | USA | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18955 | hp1 | a0001 | c0001 | t0007 | g0073 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| 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:17375961
|
ACCG | A | 3 | a0005a0007a0008 | 6 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
disruptive_inframe_deletion | MODERATE | c.216_218delGCC | p.Pro73del | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/9 | 774/9044 | 216/4956 | 72/1651 | INFO_REALIGN_3_PRIME | chrX | 17375961 | |
| chrX:17375968
|
C | T | 2 | a0006a0013 | 5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
missense_variant | MODERATE | c.211C>T | p.Pro71Ser | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/9 | 769/9044 | 211/4956 | 71/1651 | chrX | 17375968 | ||
| chrX:17376059
|
AGGCGGCG others(29): Show |
A | 1 | a0013 | 1 | HG02630.hp2 | conservative_inframe_deletion | MODERATE | c.310_345delCCCGCAGC others(28): Show |
p.Pro104_Ala115del | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/9 | 868/9044 | 310/4956 | 104/1651 | INFO_REALIGN_3_PRIME | chrX | 17376059 | |
| chrX:17725820
|
C | T | 3 | a0004a0008a0012 | 7 | HG01071.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
missense_variant | MODERATE | c.1714C>T | p.Pro572Ser | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/9 | 2272/9044 | 1714/4956 | 572/1651 | chrX | 17725820 | ||
| chrX:17725829
|
A | G | 1 | a0012 | 1 | HG01071.hp2 | missense_variant | MODERATE | c.1723A>G | p.Lys575Glu | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/9 | 2281/9044 | 1723/4956 | 575/1651 | chrX | 17725829 | ||
| chrX:17726716
|
G | C | 1 | a0007 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.2610G>C | p.Lys870Asn | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/9 | 3168/9044 | 2610/4956 | 870/1651 | chrX | 17726716 | ||
| chrX:17726838
|
A | G | 1 | a0011 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.2732A>G | p.Glu911Gly | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/9 | 3290/9044 | 2732/4956 | 911/1651 | chrX | 17726838 | ||
| chrX:17726937
|
A | T | 2 | a0003a0010 | 6 | HG01952.hp1 HG02300.hp1 NA18948.hp1 others(3): Show |
missense_variant | MODERATE | c.2831A>T | p.His944Leu | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/9 | 3389/9044 | 2831/4956 | 944/1651 | chrX | 17726937 | ||
| chrX:17727651
|
C | T | 1 | a0010 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.3545C>T | p.Pro1182Leu | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/9 | 4103/9044 | 3545/4956 | 1182/1651 | chrX | 17727651 | ||
| chrX:17728124
|
T | C | 11 | a0001a0003a0004others(8): Show | 97 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(94): Show |
missense_variant | MODERATE | c.4018T>C | p.Phe1340Leu | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/9 | 4576/9044 | 4018/4956 | 1340/1651 | chrX | 17728124 | ||
| chrX:17732340
|
G | C | 1 | a0009 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.4832G>C | p.Ser1611Thr | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 5390/9044 | 4832/4956 | 1611/1651 | chrX | 17732340 |
| 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:17692381
|
C | G | 1 | a0002c0015 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.765C>G | p.Pro255Pro | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/9 | 1323/9044 | 765/4956 | 255/1651 | chrX | 17692381 | ||
| chrX:17727307
|
T | C | 2 | a0001c0003a0006c0007 | 7 | HG01258.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
synonymous_variant | LOW | c.3201T>C | p.Ser1067Ser | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/9 | 3759/9044 | 3201/4956 | 1067/1651 | chrX | 17727307 | ||
| chrX:17727310
|
A | G | 2 | a0001c0003a0006c0007 | 7 | HG01258.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
synonymous_variant | LOW | c.3204A>G | p.Leu1068Leu | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/9 | 3762/9044 | 3204/4956 | 1068/1651 | chrX | 17727310 |
| 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:17375203
|
G | A | 1 | a0002c0002t0011 | 1 | HG02257.hp1 | 5_prime_UTR_variant | MODIFIER | c.-555G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/9 | 555 | chrX | 17375203 | |||||
| chrX:17375303
|
C | CG | 3 | a0001c0001t0006a0001c0001t0012a0002c0002t0006 | 3 | NA19000.hp1 NA19030.hp1 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-451dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/9 | 450 | INFO_REALIGN_3_PRIME | chrX | 17375303 | ||||
| chrX:17733118
|
G | A | 1 | a0001c0001t0007 | 2 | NA18955.hp1 NA19076.hp1 |
3_prime_UTR_variant | MODIFIER | c.*654G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 654 | chrX | 17733118 | |||||
| chrX:17733300
|
AT | A | 2 | a0005c0006t0008a0006c0008t0008 | 2 | HG02145.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*846delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 846 | INFO_REALIGN_3_PRIME | chrX | 17733300 | ||||
| chrX:17733838
|
A | T | 15 | a0001c0001t0002a0001c0001t0005a0001c0001t0012others(12): Show | 40 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1374A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 1374 | chrX | 17733838 | |||||
| chrX:17733999
|
C | T | 1 | a0001c0001t0004 | 3 | HG01261.hp1 NA18970.hp1 NA19063.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1535C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 1535 | chrX | 17733999 | |||||
| chrX:17734655
|
C | T | 17 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(14): Show | 43 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2191C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 2191 | chrX | 17734655 | |||||
| chrX:17734817
|
T | C | 1 | a0001c0001t0013 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2353T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 2353 | chrX | 17734817 | |||||
| chrX:17734833
|
AT | A | 1 | a0002c0002t0014 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2372delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 2372 | INFO_REALIGN_3_PRIME | chrX | 17734833 | ||||
| chrX:17734891
|
T | C | 2 | a0001c0001t0005a0005c0006t0005 | 3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2427T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 2427 | chrX | 17734891 | |||||
| chrX:17734989
|
A | ATTAAT | 2 | a0001c0001t0005a0005c0006t0005 | 3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2529_*2530insTTTA others(1): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 2530 | INFO_REALIGN_3_PRIME | chrX | 17734989 | ||||
| chrX:17735280
|
T | G | 6 | a0001c0001t0012a0001c0001t0017a0004c0005t0003others(3): Show | 9 | HG01071.hp2 HG01975.hp1 HG02055.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2816T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 2816 | chrX | 17735280 | |||||
| chrX:17735303
|
T | G | 1 | a0001c0001t0015 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2839T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 2839 | chrX | 17735303 | |||||
| chrX:17735304
|
T | TTAAGCCG others(6): Show |
1 | a0001c0001t0015 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2840_*2841insTAAG others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 2841 | chrX | 17735304 | |||||
| chrX:17735306
|
G | C | 1 | a0001c0001t0015 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2842G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 2842 | chrX | 17735306 | |||||
| chrX:17735472
|
T | A | 4 | a0004c0005t0003a0004c0005t0010a0008c0010t0003others(1): Show | 7 | HG01071.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3008T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 3008 | chrX | 17735472 | |||||
| chrX:17735718
|
T | C | 3 | a0004c0005t0003a0008c0010t0003a0012c0014t0003 | 5 | HG01071.hp2 HG02055.hp1 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3254T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 3254 | chrX | 17735718 | |||||
| chrX:17735861
|
TAA | T | 1 | a0002c0002t0016 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3398_*3399delAA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 3398 | chrX | 17735861 |
| 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:17376857
|
C | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+535C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17376857 | ||||||
| chrX:17376951
|
T | C | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.565+629T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17376951 | ||||||
| chrX:17377378
|
C | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+1056C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17377378 | ||||||
| chrX:17377548
|
C | G | 1 | a0001c0001t0004g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.565+1226C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17377548 | ||||||
| chrX:17377641
|
GTGTTC | G | 1 | a0002c0002t0001g0003 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.565+1321_565+1325d others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17377641 | |||||
| chrX:17377688
|
C | G | 6 | a0005c0006t0001g0157a0005c0006t0001g0162a0005c0006t0005g0159others(3): Show | 6 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+1366C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17377688 | ||||||
| chrX:17377823
|
CG | C | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.565+1505delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17377823 | |||||
| chrX:17378059
|
C | CGT | 61 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(58): Show | 61 | HG00609.hp1 HG01069.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.565+1763_565+1764d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | |||||
| chrX:17378059
|
C | CGTGT | 11 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(8): Show | 11 | HG02258.hp1 HG02622.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.565+1761_565+1764d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | |||||
| chrX:17378059
|
C | CGTGTGT | 2 | a0001c0001t0002g0002a0005c0006t0001g0162 | 2 | HG02293.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.565+1759_565+1764d others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | |||||
| chrX:17378059
|
C | CGTGTGTG others(5): Show |
4 | a0001c0001t0006g0112a0006c0007t0002g0115a0006c0008t0001g0114others(1): Show | 4 | HG02145.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+1753_565+1764d others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | |||||
| chrX:17378059
|
C | CGTGTGTG others(7): Show |
1 | a0001c0001t0002g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.565+1751_565+1764d others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | |||||
| chrX:17378059
|
C | CGTGTGTG others(9): Show |
3 | a0004c0005t0003g0117a0006c0007t0002g0118a0013c0016t0002g0119 | 3 | HG02615.hp1 HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.565+1749_565+1764d others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | |||||
| chrX:17378059
|
C | CGTGTGTG others(11): Show |
1 | a0001c0001t0002g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.565+1747_565+1764d others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | |||||
| chrX:17378059
|
C | CGTGTGTG others(13): Show |
4 | a0001c0001t0001g0124a0001c0001t0002g0121a0001c0001t0009g0122others(1): Show | 4 | HG00639.hp1 HG01943.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+1745_565+1764d others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | |||||
| chrX:17378059
|
C | CGTGTGTG others(15): Show |
11 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0133others(8): Show | 11 | HG00738.hp1 HG01071.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.565+1743_565+1764d others(24): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | |||||
| chrX:17378059
|
C | CGTGTGTG others(17): Show |
12 | a0001c0001t0001g0137a0001c0001t0001g0140a0001c0001t0001g0144others(9): Show | 12 | HG00639.hp2 HG00673.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.565+1741_565+1764d others(26): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | |||||
| chrX:17378059
|
C | CGTGTGTG others(19): Show |
7 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0017g0154others(4): Show | 7 | HG00408.hp1 HG00642.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+1739_565+1764d others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | |||||
| chrX:17378059
|
C | CGTGTGTG others(23): Show |
1 | a0001c0003t0002g0155 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.565+1764_565+1765i others(32): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | |||||
| chrX:17378059
|
C | CGTGTGTG others(25): Show |
1 | a0002c0002t0001g0156 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.565+1764_565+1765i others(34): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | |||||
| chrX:17378059
|
CGT | C | 31 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(28): Show | 31 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.565+1763_565+1764d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | |||||
| chrX:17378099
|
CCTT | C | 5 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+1778_565+1780d others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17378099 | ||||||
| chrX:17378144
|
ATG | A | 4 | a0001c0001t0001g0127a0001c0001t0002g0126a0001c0001t0009g0125others(1): Show | 4 | HG01071.hp1 HG02647.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+1825_565+1826d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378144 | |||||
| chrX:17378248
|
ATAGT | A | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+1931_565+1934d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378248 | |||||
| chrX:17378918
|
A | G | 7 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(4): Show | 7 | HG02257.hp2 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+2596A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17378918 | ||||||
| chrX:17379337
|
C | T | 2 | a0001c0001t0002g0146a0009c0011t0002g0147 | 2 | HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+3015C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17379337 | ||||||
| chrX:17379380
|
T | G | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.565+3058T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17379380 | ||||||
| chrX:17379555
|
G | A | 5 | a0006c0007t0002g0115a0006c0007t0002g0118a0006c0008t0001g0114others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+3233G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17379555 | ||||||
| chrX:17379573
|
G | GT | 1 | a0001c0001t0001g0104 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.565+3251_565+3252i others(3): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17379573 | ||||||
| chrX:17379634
|
G | A | 1 | a0006c0007t0002g0118 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565+3312G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17379634 | ||||||
| chrX:17379905
|
G | C | 5 | a0006c0007t0002g0115a0006c0007t0002g0118a0006c0008t0001g0114others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+3583G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17379905 | ||||||
| chrX:17380038
|
G | C | 1 | a0002c0002t0001g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.565+3716G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17380038 | ||||||
| chrX:17380378
|
C | CT | 38 | a0001c0001t0001g0124a0001c0001t0001g0127a0001c0001t0001g0129others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.565+4071dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17380378 | |||||
| chrX:17380378
|
CT | C | 51 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(48): Show | 51 | HG00609.hp1 HG01358.hp1 HG02015.hp1 others(48): Show |
intron_variant | MODIFIER | c.565+4071delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17380378 | |||||
| chrX:17380608
|
A | G | 1 | a0001c0001t0006g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.565+4286A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17380608 | ||||||
| chrX:17381118
|
G | A | 6 | a0005c0006t0001g0157a0005c0006t0001g0162a0005c0006t0005g0159others(3): Show | 6 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+4796G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17381118 | ||||||
| chrX:17381259
|
G | A | 33 | a0001c0001t0001g0124a0001c0001t0001g0127a0001c0001t0001g0129others(30): Show | 33 | HG00408.hp1 HG00639.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.565+4937G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17381259 | ||||||
| chrX:17381336
|
C | T | 1 | a0002c0002t0001g0033 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.565+5014C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17381336 | ||||||
| chrX:17381347
|
G | A | 1 | a0002c0002t0001g0156 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.565+5025G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17381347 | ||||||
| chrX:17381462
|
A | G | 3 | a0002c0002t0001g0087a0002c0002t0001g0088a0002c0002t0001g0089 | 3 | HG02129.hp1 NA18945.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.565+5140A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17381462 | ||||||
| chrX:17381743
|
A | T | 1 | a0001c0001t0005g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.565+5421A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17381743 | ||||||
| chrX:17381977
|
C | T | 1 | a0001c0003t0002g0155 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.565+5655C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17381977 | ||||||
| chrX:17382025
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.565+5703C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17382025 | ||||||
| chrX:17382061
|
CT | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+5742delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17382061 | |||||
| chrX:17382184
|
G | A | 1 | a0002c0002t0001g0105 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.565+5862G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17382184 | ||||||
| chrX:17383069
|
A | T | 4 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0144others(1): Show | 4 | NA18994.hp1 NA18995.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+6747A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17383069 | ||||||
| chrX:17383107
|
T | C | 5 | a0006c0007t0002g0115a0006c0007t0002g0118a0006c0008t0001g0114others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+6785T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17383107 | ||||||
| chrX:17383846
|
G | T | 1 | a0001c0001t0002g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.565+7524G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17383846 | ||||||
| chrX:17384154
|
G | A | 4 | a0001c0001t0002g0004a0001c0001t0002g0093a0002c0002t0001g0091others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+7832G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17384154 | ||||||
| chrX:17384545
|
A | G | 5 | a0006c0007t0002g0115a0006c0007t0002g0118a0006c0008t0001g0114others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+8223A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17384545 | ||||||
| chrX:17384813
|
AATTTT | A | 6 | a0005c0006t0001g0157a0005c0006t0001g0162a0005c0006t0005g0159others(3): Show | 6 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+8496_565+8500d others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17384813 | |||||
| chrX:17384933
|
C | CA | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+8616dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17384933 | |||||
| chrX:17385041
|
T | C | 38 | a0001c0001t0001g0124a0001c0001t0001g0127a0001c0001t0001g0129others(35): Show | 38 | HG00408.hp1 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.565+8719T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17385041 | ||||||
| chrX:17385674
|
A | G | 5 | a0006c0007t0002g0115a0006c0007t0002g0118a0006c0008t0001g0114others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+9352A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17385674 | ||||||
| chrX:17385701
|
G | A | 1 | a0001c0003t0002g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.565+9379G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17385701 | ||||||
| chrX:17386222
|
G | A | 9 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(6): Show | 9 | HG02056.hp1 NA18612.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.565+9900G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17386222 | ||||||
| chrX:17386263
|
A | G | 2 | a0002c0002t0001g0054a0003c0004t0001g0055 | 2 | HG02056.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.565+9941A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17386263 | ||||||
| chrX:17386331
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.565+10009G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17386331 | ||||||
| chrX:17386442
|
C | CT | 1 | a0002c0015t0001g0046 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.565+10122dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17386442 | |||||
| chrX:17386534
|
C | T | 2 | a0001c0001t0002g0085a0004c0005t0010g0086 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.565+10212C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17386534 | ||||||
| chrX:17386629
|
C | T | 6 | a0005c0006t0001g0157a0005c0006t0001g0162a0005c0006t0005g0159others(3): Show | 6 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+10307C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17386629 | ||||||
| chrX:17386663
|
C | CA | 58 | a0001c0001t0001g0009a0001c0001t0001g0094a0001c0001t0001g0095others(55): Show | 58 | HG00408.hp1 HG00621.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.565+10362dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17386663 | |||||
| chrX:17386663
|
C | CAA | 2 | a0001c0001t0001g0144a0001c0001t0002g0002 | 2 | HG02293.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.565+10361_565+1036 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17386663 | |||||
| chrX:17386663
|
CA | C | 2 | a0001c0001t0002g0093a0004c0005t0010g0086 | 2 | HG01069.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.565+10362delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17386663 | |||||
| chrX:17387347
|
GCAAT | G | 1 | a0002c0002t0001g0084 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.565+11028_565+1103 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17387347 | |||||
| chrX:17387616
|
G | A | 1 | a0002c0002t0001g0011 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.565+11294G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17387616 | ||||||
| chrX:17388145
|
C | T | 1 | a0005c0006t0008g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565+11823C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17388145 | ||||||
| chrX:17388294
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.565+11972G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17388294 | ||||||
| chrX:17388483
|
G | C | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+12161G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17388483 | ||||||
| chrX:17388829
|
A | C | 5 | a0006c0007t0002g0115a0006c0007t0002g0118a0006c0008t0001g0114others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+12507A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17388829 | ||||||
| chrX:17388836
|
G | A | 3 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110 | 3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+12514G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17388836 | ||||||
| chrX:17388921
|
A | C | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.565+12599A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17388921 | ||||||
| chrX:17388947
|
T | TA | 2 | a0001c0001t0002g0146a0009c0011t0002g0147 | 2 | HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+12626dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17388947 | |||||
| chrX:17389498
|
A | G | 2 | a0001c0001t0002g0002a0001c0001t0002g0096 | 2 | HG02293.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.565+13176A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17389498 | ||||||
| chrX:17389581
|
A | T | 1 | a0002c0002t0001g0010 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.565+13259A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17389581 | ||||||
| chrX:17389586
|
C | CTTAT | 97 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0038others(94): Show | 97 | HG00408.hp1 HG00621.hp1 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.565+13291_565+1329 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17389586 | |||||
| chrX:17389586
|
C | CTTATTTA others(1): Show |
9 | a0001c0001t0001g0057a0001c0001t0001g0129a0001c0001t0002g0085others(6): Show | 9 | HG00609.hp1 HG00738.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.565+13287_565+1329 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17389586 | |||||
| chrX:17389586
|
C | CTTATTTA others(5): Show |
12 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0116others(9): Show | 12 | HG01106.hp1 HG02293.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.565+13283_565+1329 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17389586 | |||||
| chrX:17389586
|
C | CTTATTTA others(9): Show |
6 | a0001c0001t0002g0096a0005c0006t0001g0162a0006c0008t0001g0114others(3): Show | 6 | HG02257.hp2 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+13279_565+1329 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17389586 | |||||
| chrX:17389586
|
C | CTTATTTA others(13): Show |
2 | a0001c0001t0002g0146a0006c0008t0008g0113 | 2 | HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.565+13275_565+1329 others(24): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17389586 | |||||
| chrX:17389666
|
A | G | 1 | a0002c0002t0001g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.565+13344A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17389666 | ||||||
| chrX:17389813
|
G | T | 1 | a0001c0001t0001g0083 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.565+13491G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17389813 | ||||||
| chrX:17389848
|
C | A | 2 | a0001c0001t0013g0059a0002c0002t0006g0060 | 2 | NA18965.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.565+13526C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17389848 | ||||||
| chrX:17389919
|
C | T | 4 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0005g0103others(1): Show | 4 | HG02280.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+13597C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17389919 | ||||||
| chrX:17389943
|
A | T | 2 | a0001c0001t0002g0002a0001c0001t0002g0096 | 2 | HG02293.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.565+13621A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17389943 | ||||||
| chrX:17389944
|
A | T | 2 | a0001c0001t0002g0002a0001c0001t0002g0096 | 2 | HG02293.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.565+13622A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17389944 | ||||||
| chrX:17389952
|
G | GA | 6 | a0005c0006t0001g0157a0005c0006t0001g0162a0005c0006t0005g0159others(3): Show | 6 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+13642dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17389952 | |||||
| chrX:17389952
|
GA | G | 1 | a0002c0002t0001g0006 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.565+13642delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17389952 | |||||
| chrX:17390052
|
T | C | 1 | a0002c0002t0001g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.565+13730T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17390052 | ||||||
| chrX:17390060
|
G | A | 2 | a0001c0001t0013g0059a0002c0002t0006g0060 | 2 | NA18965.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.565+13738G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17390060 | ||||||
| chrX:17390323
|
G | A | 4 | a0001c0001t0001g0061a0001c0001t0001g0090a0001c0001t0001g0098others(1): Show | 4 | NA18967.hp1 NA18983.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+14001G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17390323 | ||||||
| chrX:17390460
|
G | A | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+14138G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17390460 | ||||||
| chrX:17390512
|
T | C | 35 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0124others(32): Show | 35 | HG00408.hp1 HG00621.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.565+14190T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17390512 | ||||||
| chrX:17390848
|
C | T | 34 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0124others(31): Show | 34 | HG00408.hp1 HG00621.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.565+14526C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17390848 | ||||||
| chrX:17391001
|
T | C | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.565+14679T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17391001 | ||||||
| chrX:17391023
|
G | T | 1 | a0001c0001t0001g0009 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.565+14701G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17391023 | ||||||
| chrX:17391117
|
A | G | 2 | a0001c0001t0002g0002a0001c0001t0002g0096 | 2 | HG02293.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.565+14795A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17391117 | ||||||
| chrX:17391214
|
G | T | 4 | a0001c0001t0002g0004a0001c0001t0002g0093a0002c0002t0001g0091others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+14892G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17391214 | ||||||
| chrX:17391516
|
A | C | 2 | a0001c0001t0002g0002a0001c0001t0002g0096 | 2 | HG02293.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.565+15194A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17391516 | ||||||
| chrX:17392070
|
G | A | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.565+15748G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17392070 | ||||||
| chrX:17392246
|
G | A | 7 | a0001c0001t0002g0002a0001c0001t0002g0096a0006c0007t0002g0115others(4): Show | 7 | HG02145.hp1 HG02293.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+15924G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17392246 | ||||||
| chrX:17392717
|
C | A | 1 | a0003c0004t0001g0013 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.565+16395C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17392717 | ||||||
| chrX:17393028
|
A | G | 1 | a0002c0002t0001g0008 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.565+16706A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17393028 | ||||||
| chrX:17393102
|
TG | T | 5 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+16783delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17393102 | |||||
| chrX:17393194
|
C | G | 1 | a0002c0002t0001g0082 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.565+16872C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17393194 | ||||||
| chrX:17393363
|
G | A | 4 | a0001c0001t0001g0127a0001c0001t0002g0126a0001c0001t0009g0125others(1): Show | 4 | HG01071.hp1 HG02647.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+17041G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17393363 | ||||||
| chrX:17393386
|
G | A | 5 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+17064G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17393386 | ||||||
| chrX:17393556
|
C | T | 2 | a0001c0001t0002g0002a0001c0001t0002g0096 | 2 | HG02293.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.565+17234C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17393556 | ||||||
| chrX:17393726
|
G | T | 2 | a0001c0001t0002g0002a0001c0001t0002g0096 | 2 | HG02293.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.565+17404G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17393726 | ||||||
| chrX:17393956
|
C | T | 1 | a0001c0001t0012g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.565+17634C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17393956 | ||||||
| chrX:17394085
|
A | G | 1 | a0001c0001t0002g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.565+17763A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17394085 | ||||||
| chrX:17394274
|
T | C | 1 | a0006c0008t0001g0114 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.565+17952T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17394274 | ||||||
| chrX:17394321
|
T | C | 2 | a0001c0001t0002g0002a0001c0001t0002g0096 | 2 | HG02293.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.565+17999T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17394321 | ||||||
| chrX:17394411
|
CT | C | 1 | a0002c0002t0001g0062 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.565+18092delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17394411 | |||||
| chrX:17394637
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+18315C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17394637 | ||||||
| chrX:17394726
|
C | G | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+18404C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17394726 | ||||||
| chrX:17394771
|
G | T | 10 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(7): Show | 10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+18449G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17394771 | ||||||
| chrX:17394772
|
A | AT | 10 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(7): Show | 10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+18456dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17394772 | |||||
| chrX:17394997
|
A | G | 1 | a0001c0003t0002g0142 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.565+18675A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17394997 | ||||||
| chrX:17395179
|
GA | G | 6 | a0001c0001t0001g0081a0001c0001t0002g0116a0001c0001t0002g0120others(3): Show | 6 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+18869delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17395179 | |||||
| chrX:17396318
|
C | CT | 5 | a0006c0007t0002g0115a0006c0007t0002g0118a0006c0008t0001g0114others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+20002dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17396318 | |||||
| chrX:17396463
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.565+20141G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17396463 | ||||||
| chrX:17396781
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0124a0002c0002t0001g0031others(1): Show | 4 | HG01099.hp1 HG01928.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+20459C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17396781 | ||||||
| chrX:17397143
|
A | G | 1 | a0002c0002t0001g0080 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.565+20821A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17397143 | ||||||
| chrX:17397331
|
T | C | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+21009T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17397331 | ||||||
| chrX:17397611
|
G | A | 5 | a0001c0001t0002g0002a0001c0001t0002g0099a0001c0001t0002g0146others(2): Show | 5 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+21289G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17397611 | ||||||
| chrX:17398874
|
C | G | 1 | a0004c0005t0003g0117 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.565+22552C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17398874 | ||||||
| chrX:17398938
|
A | G | 5 | a0006c0007t0002g0115a0006c0007t0002g0118a0006c0008t0001g0114others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+22616A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17398938 | ||||||
| chrX:17399180
|
C | T | 1 | a0002c0002t0001g0141 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.565+22858C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17399180 | ||||||
| chrX:17400043
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.565+23721A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17400043 | ||||||
| chrX:17400064
|
C | A | 5 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+23742C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17400064 | ||||||
| chrX:17400200
|
T | C | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+23878T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17400200 | ||||||
| chrX:17400367
|
T | C | 9 | a0001c0001t0002g0002a0001c0001t0002g0099a0001c0001t0002g0146others(6): Show | 9 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+24045T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17400367 | ||||||
| chrX:17400511
|
G | A | 5 | a0006c0007t0002g0115a0006c0007t0002g0118a0006c0008t0001g0114others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+24189G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17400511 | ||||||
| chrX:17400591
|
GA | G | 1 | a0002c0002t0001g0141 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.565+24280delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17400591 | |||||
| chrX:17401192
|
A | C | 1 | a0001c0001t0002g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.565+24870A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17401192 | ||||||
| chrX:17401289
|
A | G | 5 | a0006c0007t0002g0115a0006c0007t0002g0118a0006c0008t0001g0114others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+24967A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17401289 | ||||||
| chrX:17401775
|
CTTA | C | 1 | a0004c0005t0003g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.565+25458_565+2546 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17401775 | |||||
| chrX:17401894
|
TG | T | 1 | a0002c0002t0001g0148 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.565+25576delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17401894 | |||||
| chrX:17401913
|
T | C | 5 | a0006c0007t0002g0115a0006c0007t0002g0118a0006c0008t0001g0114others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+25591T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17401913 | ||||||
| chrX:17402010
|
T | C | 4 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0144others(1): Show | 4 | NA18994.hp1 NA18995.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+25688T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17402010 | ||||||
| chrX:17402223
|
T | C | 9 | a0001c0001t0002g0002a0001c0001t0002g0099a0001c0001t0002g0146others(6): Show | 9 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+25901T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17402223 | ||||||
| chrX:17402320
|
G | C | 1 | a0006c0007t0002g0118 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565+25998G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17402320 | ||||||
| chrX:17402553
|
A | G | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+26231A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17402553 | ||||||
| chrX:17402629
|
G | T | 1 | a0002c0002t0001g0003 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.565+26307G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17402629 | ||||||
| chrX:17402894
|
G | C | 1 | a0002c0002t0001g0014 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.565+26572G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17402894 | ||||||
| chrX:17403025
|
C | G | 2 | a0006c0008t0001g0114a0006c0008t0008g0113 | 2 | HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.565+26703C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17403025 | ||||||
| chrX:17403448
|
A | G | 8 | a0001c0001t0002g0099a0001c0001t0002g0146a0006c0007t0002g0115others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.565+27126A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17403448 | ||||||
| chrX:17403893
|
A | G | 8 | a0001c0001t0005g0111a0001c0003t0002g0101a0005c0006t0001g0157others(5): Show | 8 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.565+27571A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17403893 | ||||||
| chrX:17404024
|
A | T | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.565+27702A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17404024 | ||||||
| chrX:17404482
|
T | C | 1 | a0002c0002t0001g0014 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.565+28160T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17404482 | ||||||
| chrX:17404652
|
C | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+28330C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17404652 | ||||||
| chrX:17404792
|
C | T | 8 | a0001c0001t0005g0111a0001c0003t0002g0101a0005c0006t0001g0157others(5): Show | 8 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.565+28470C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17404792 | ||||||
| chrX:17404801
|
CTG | C | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+28481_565+2848 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17404801 | |||||
| chrX:17404803
|
G | GTC | 15 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0144others(12): Show | 15 | HG01106.hp1 HG01975.hp2 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.565+28508_565+2850 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17404803 | |||||
| chrX:17404803
|
G | GTCTC | 3 | a0001c0001t0002g0085a0001c0001t0004g0163a0004c0005t0010g0086 | 3 | HG01261.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.565+28506_565+2850 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17404803 | |||||
| chrX:17404803
|
GTCTC | G | 1 | a0001c0001t0001g0081 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.565+28506_565+2850 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17404803 | |||||
| chrX:17405033
|
A | G | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+28711A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17405033 | ||||||
| chrX:17405105
|
G | A | 6 | a0005c0006t0001g0157a0005c0006t0001g0162a0005c0006t0005g0159others(3): Show | 6 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+28783G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17405105 | ||||||
| chrX:17405593
|
T | G | 1 | a0002c0002t0014g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.565+29271T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17405593 | ||||||
| chrX:17405594
|
C | T | 1 | a0002c0002t0014g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.565+29272C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17405594 | ||||||
| chrX:17405645
|
A | AT | 5 | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0124others(2): Show | 5 | HG01099.hp1 HG01928.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+29329dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17405645 | |||||
| chrX:17405835
|
A | G | 4 | a0001c0001t0002g0002a0001c0001t0002g0099a0001c0001t0002g0146others(1): Show | 4 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+29513A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17405835 | ||||||
| chrX:17405885
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.565+29563A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17405885 | ||||||
| chrX:17405996
|
C | T | 64 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(61): Show | 64 | HG00609.hp1 HG01069.hp1 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.565+29674C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17405996 | ||||||
| chrX:17406558
|
A | C | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+30236A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17406558 | ||||||
| chrX:17406600
|
C | T | 1 | a0002c0002t0001g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.565+30278C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17406600 | ||||||
| chrX:17406689
|
G | A | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+30367G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17406689 | ||||||
| chrX:17407121
|
AG | A | 1 | a0002c0002t0001g0015 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.565+30800delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17407121 | ||||||
| chrX:17407136
|
TC | T | 1 | a0001c0001t0001g0081 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.565+30815delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17407136 | ||||||
| chrX:17407232
|
T | C | 1 | a0001c0001t0017g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.565+30910T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17407232 | ||||||
| chrX:17407438
|
C | G | 4 | a0001c0001t0002g0002a0001c0001t0002g0099a0001c0001t0002g0146others(1): Show | 4 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+31116C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17407438 | ||||||
| chrX:17407568
|
T | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+31246T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17407568 | ||||||
| chrX:17408103
|
G | A | 1 | a0001c0001t0009g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.565+31781G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17408103 | ||||||
| chrX:17408162
|
T | C | 37 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(34): Show | 37 | HG00280.hp1 HG00408.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.565+31840T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17408162 | ||||||
| chrX:17408576
|
C | T | 11 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(8): Show | 11 | HG01256.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.565+32254C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17408576 | ||||||
| chrX:17408711
|
G | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+32389G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17408711 | ||||||
| chrX:17408806
|
C | T | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+32484C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17408806 | ||||||
| chrX:17408951
|
AGAG | A | 2 | a0001c0001t0002g0085a0004c0005t0010g0086 | 2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.565+32633_565+3263 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17408951 | |||||
| chrX:17408954
|
G | GGA | 10 | a0001c0001t0001g0127a0001c0001t0002g0099a0001c0001t0002g0106others(7): Show | 10 | HG01071.hp1 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+32656_565+3265 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17408954 | |||||
| chrX:17408954
|
G | GGAGAGAG others(1): Show |
1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+32650_565+3265 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17408954 | |||||
| chrX:17408954
|
GGAGA | G | 18 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(15): Show | 18 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.565+32654_565+3265 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17408954 | |||||
| chrX:17409374
|
G | GT | 7 | a0001c0001t0001g0090a0001c0001t0001g0133a0001c0001t0002g0002others(4): Show | 7 | HG01243.hp1 HG01975.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+33068dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17409374 | |||||
| chrX:17409374
|
G | GTT | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+33067_565+3306 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17409374 | |||||
| chrX:17409374
|
GT | G | 27 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0029others(24): Show | 27 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.565+33068delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17409374 | |||||
| chrX:17409531
|
C | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+33209C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17409531 | ||||||
| chrX:17409754
|
C | CT | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+33433dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17409754 | |||||
| chrX:17409868
|
T | C | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.565+33546T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17409868 | ||||||
| chrX:17410115
|
C | CA | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+33796dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17410115 | |||||
| chrX:17410139
|
G | C | 1 | a0001c0001t0001g0067 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.565+33817G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17410139 | ||||||
| chrX:17410218
|
G | A | 1 | a0001c0001t0009g0125 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.565+33896G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17410218 | ||||||
| chrX:17410386
|
G | A | 1 | a0002c0002t0001g0015 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.565+34064G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17410386 | ||||||
| chrX:17410463
|
T | C | 1 | a0002c0002t0001g0054 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.565+34141T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17410463 | ||||||
| chrX:17410516
|
C | CT | 27 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(24): Show | 27 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.565+34215dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17410516 | |||||
| chrX:17410516
|
C | CTT | 6 | a0001c0001t0002g0099a0001c0001t0002g0146a0001c0001t0015g0079others(3): Show | 6 | HG01243.hp1 HG02257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+34214_565+3421 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17410516 | |||||
| chrX:17410516
|
C | CTTT | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+34213_565+3421 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17410516 | |||||
| chrX:17410516
|
CT | C | 13 | a0001c0001t0001g0036a0001c0001t0002g0164a0001c0001t0012g0044others(10): Show | 13 | HG01106.hp1 HG02280.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.565+34215delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17410516 | |||||
| chrX:17410538
|
C | T | 4 | a0001c0001t0002g0002a0001c0001t0002g0099a0001c0001t0002g0146others(1): Show | 4 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+34216C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17410538 | ||||||
| chrX:17410555
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.565+34233A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17410555 | ||||||
| chrX:17410850
|
A | G | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+34528A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17410850 | ||||||
| chrX:17411106
|
G | GT | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+34788dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17411106 | |||||
| chrX:17411275
|
A | C | 23 | a0001c0001t0002g0002a0001c0001t0002g0099a0001c0001t0002g0116others(20): Show | 23 | HG01106.hp1 HG01243.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.565+34953A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17411275 | ||||||
| chrX:17411411
|
A | G | 1 | a0002c0002t0001g0023 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.565+35089A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17411411 | ||||||
| chrX:17411572
|
C | T | 3 | a0001c0001t0001g0083a0002c0002t0001g0001a0002c0002t0001g0077 | 3 | HG02040.hp1 HG02293.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.565+35250C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17411572 | ||||||
| chrX:17411610
|
A | T | 1 | a0002c0002t0001g0148 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.565+35288A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17411610 | ||||||
| chrX:17411768
|
A | G | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+35446A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17411768 | ||||||
| chrX:17411888
|
G | A | 10 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(7): Show | 10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+35566G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17411888 | ||||||
| chrX:17411944
|
T | G | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+35622T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17411944 | ||||||
| chrX:17412143
|
A | ATC | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35822_565+3582 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17412143 | |||||
| chrX:17412145
|
G | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35823G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412145 | ||||||
| chrX:17412146
|
G | T | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35824G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412146 | ||||||
| chrX:17412147
|
A | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35825A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412147 | ||||||
| chrX:17412149
|
G | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35827G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412149 | ||||||
| chrX:17412151
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35829G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412151 | ||||||
| chrX:17412152
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35830T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412152 | ||||||
| chrX:17412157
|
T | A | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35835T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412157 | ||||||
| chrX:17412158
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35836T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412158 | ||||||
| chrX:17412160
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35838G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412160 | ||||||
| chrX:17412161
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35839T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412161 | ||||||
| chrX:17412163
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35841T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412163 | ||||||
| chrX:17412164
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35842G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412164 | ||||||
| chrX:17412166
|
C | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35844C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412166 | ||||||
| chrX:17412167
|
T | A | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35845T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412167 | ||||||
| chrX:17412168
|
C | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35846C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412168 | ||||||
| chrX:17412169
|
C | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35847C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412169 | ||||||
| chrX:17412170
|
AT | A | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35851delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17412170 | |||||
| chrX:17412172
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35850T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412172 | ||||||
| chrX:17412173
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35851T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412173 | ||||||
| chrX:17412174
|
C | A | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35852C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412174 | ||||||
| chrX:17412177
|
T | A | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35855T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412177 | ||||||
| chrX:17412180
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35858T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412180 | ||||||
| chrX:17412182
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35860T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412182 | ||||||
| chrX:17412183
|
T | A | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35861T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412183 | ||||||
| chrX:17412184
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35862T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412184 | ||||||
| chrX:17412188
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35866T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412188 | ||||||
| chrX:17412190
|
CT | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35870delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17412190 | |||||
| chrX:17412194
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35872A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412194 | ||||||
| chrX:17412197
|
A | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35875A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412197 | ||||||
| chrX:17412198
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35876A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412198 | ||||||
| chrX:17412199
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35877T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412199 | ||||||
| chrX:17412201
|
T | TG | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35879_565+3588 others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412201 | ||||||
| chrX:17412202
|
A | T | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35880A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412202 | ||||||
| chrX:17412209
|
T | TC | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35887_565+3588 others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412209 | ||||||
| chrX:17412210
|
A | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35888A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412210 | ||||||
| chrX:17412212
|
A | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35890A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412212 | ||||||
| chrX:17412213
|
A | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35891A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412213 | ||||||
| chrX:17412214
|
T | TC | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35892_565+3589 others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412214 | ||||||
| chrX:17412215
|
A | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35893A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412215 | ||||||
| chrX:17412217
|
A | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35895A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412217 | ||||||
| chrX:17412218
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35896T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412218 | ||||||
| chrX:17412219
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35897A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412219 | ||||||
| chrX:17412222
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35900A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412222 | ||||||
| chrX:17412223
|
TA | T | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35902delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412223 | ||||||
| chrX:17412226
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35904A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412226 | ||||||
| chrX:17412228
|
TAA | T | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35907_565+3590 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412228 | ||||||
| chrX:17412232
|
A | T | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35910A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412232 | ||||||
| chrX:17412234
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35912A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412234 | ||||||
| chrX:17412236
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35914T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412236 | ||||||
| chrX:17412238
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35916T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412238 | ||||||
| chrX:17412240
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35918T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412240 | ||||||
| chrX:17412243
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35921G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412243 | ||||||
| chrX:17412244
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35922T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412244 | ||||||
| chrX:17412246
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35924T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412246 | ||||||
| chrX:17412248
|
C | A | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35926C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412248 | ||||||
| chrX:17412249
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35927T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412249 | ||||||
| chrX:17412253
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35931A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412253 | ||||||
| chrX:17412254
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35932T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412254 | ||||||
| chrX:17412255
|
C | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35933C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412255 | ||||||
| chrX:17412256
|
A | T | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35934A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412256 | ||||||
| chrX:17412257
|
T | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35935T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412257 | ||||||
| chrX:17412258
|
A | T | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35936A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412258 | ||||||
| chrX:17412262
|
A | G | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+35940A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412262 | ||||||
| chrX:17412343
|
C | G | 1 | a0001c0001t0017g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.565+36021C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412343 | ||||||
| chrX:17412366
|
C | T | 1 | a0002c0002t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.565+36044C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412366 | ||||||
| chrX:17412423
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.565+36101C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412423 | ||||||
| chrX:17412481
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.565+36159C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412481 | ||||||
| chrX:17412553
|
CGT | C | 1 | a0002c0002t0001g0010 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.565+36232_565+3623 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412553 | ||||||
| chrX:17412557
|
AC | A | 1 | a0002c0002t0001g0010 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.565+36236delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412557 | ||||||
| chrX:17412559
|
T | G | 1 | a0002c0002t0001g0010 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.565+36237T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412559 | ||||||
| chrX:17412827
|
G | T | 1 | a0007c0009t0002g0160 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.565+36505G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412827 | ||||||
| chrX:17412893
|
C | T | 1 | a0002c0002t0014g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.565+36571C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412893 | ||||||
| chrX:17412902
|
C | T | 7 | a0001c0003t0002g0128a0005c0006t0001g0157a0005c0006t0001g0162others(4): Show | 7 | HG01106.hp1 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.565+36580C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412902 | ||||||
| chrX:17413526
|
A | G | 19 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(16): Show | 19 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.565+37204A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17413526 | ||||||
| chrX:17413755
|
TAGAC | T | 1 | a0002c0002t0001g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.565+37436_565+3743 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17413755 | |||||
| chrX:17413781
|
A | C | 1 | a0002c0002t0001g0076 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.565+37459A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17413781 | ||||||
| chrX:17413982
|
T | C | 2 | a0002c0002t0001g0054a0003c0004t0001g0055 | 2 | HG02056.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.565+37660T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17413982 | ||||||
| chrX:17413993
|
TC | T | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+37673delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17413993 | |||||
| chrX:17413997
|
GT | G | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+37681delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17413997 | |||||
| chrX:17414089
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+37767A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17414089 | ||||||
| chrX:17414386
|
C | T | 1 | a0002c0002t0014g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.565+38064C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17414386 | ||||||
| chrX:17414986
|
G | C | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+38664G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17414986 | ||||||
| chrX:17414988
|
C | T | 7 | a0001c0003t0002g0128a0005c0006t0001g0157a0005c0006t0001g0162others(4): Show | 7 | HG01106.hp1 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.565+38666C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17414988 | ||||||
| chrX:17415194
|
G | A | 23 | a0001c0001t0002g0002a0001c0001t0002g0099a0001c0001t0002g0116others(20): Show | 23 | HG01106.hp1 HG01243.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.565+38872G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17415194 | ||||||
| chrX:17415279
|
T | C | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+38957T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17415279 | ||||||
| chrX:17415349
|
A | C | 1 | a0002c0002t0001g0035 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.565+39027A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17415349 | ||||||
| chrX:17415769
|
A | C | 4 | a0001c0001t0002g0002a0001c0001t0002g0099a0001c0001t0002g0146others(1): Show | 4 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+39447A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17415769 | ||||||
| chrX:17415824
|
CT | C | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+39509delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17415824 | |||||
| chrX:17416030
|
C | T | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+39708C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17416030 | ||||||
| chrX:17416551
|
T | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+40229T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17416551 | ||||||
| chrX:17416671
|
C | T | 49 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(46): Show | 49 | HG00609.hp1 HG01358.hp1 HG02015.hp1 others(46): Show |
intron_variant | MODIFIER | c.565+40349C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17416671 | ||||||
| chrX:17416792
|
A | ATG | 3 | a0001c0001t0002g0143a0002c0002t0001g0053a0002c0002t0001g0075 | 3 | HG04228.hp1 HG06807.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.565+40497_565+4049 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17416792 | |||||
| chrX:17416815
|
T | TGAGA | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.565+40494_565+4049 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17416815 | |||||
| chrX:17416817
|
T | A | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.565+40495T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17416817 | ||||||
| chrX:17416817
|
T | TGA | 14 | a0001c0001t0001g0133a0001c0001t0002g0120a0001c0001t0006g0112others(11): Show | 14 | HG01106.hp1 HG02071.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.565+40496_565+4049 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17416817 | |||||
| chrX:17416819
|
T | A | 36 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0129others(33): Show | 36 | HG00408.hp1 HG00621.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.565+40497T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17416819 | ||||||
| chrX:17416819
|
T | TGA | 6 | a0001c0001t0002g0116a0001c0001t0005g0111a0001c0003t0002g0101others(3): Show | 6 | HG02280.hp2 HG02602.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+40520_565+4052 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17416819 | |||||
| chrX:17416819
|
T | TGTGTGTG others(5): Show |
1 | a0001c0001t0002g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.565+40498_565+4049 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17416819 | |||||
| chrX:17416819
|
T | TGTGTGTG others(9): Show |
1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.565+40498_565+4049 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17416819 | |||||
| chrX:17416819
|
T | TGTGTGTG others(9): Show |
1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+40498_565+4049 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17416819 | |||||
| chrX:17416821
|
A | T | 1 | a0001c0001t0001g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.565+40499A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17416821 | ||||||
| chrX:17417091
|
T | TAC | 13 | a0001c0001t0002g0085a0001c0001t0002g0164a0002c0002t0001g0008others(10): Show | 13 | HG01106.hp1 HG01515.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.565+40797_565+4079 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17417091 | |||||
| chrX:17417091
|
T | TACAC | 4 | a0001c0001t0005g0111a0001c0003t0002g0101a0001c0003t0002g0128others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+40795_565+4079 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17417091 | |||||
| chrX:17417091
|
T | TACACACA others(3): Show |
2 | a0001c0001t0002g0099a0009c0011t0002g0147 | 2 | HG01243.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.565+40789_565+4079 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17417091 | |||||
| chrX:17417091
|
T | TACACACA others(5): Show |
1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+40787_565+4079 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17417091 | |||||
| chrX:17417091
|
TAC | T | 11 | a0001c0001t0002g0043a0001c0001t0002g0116a0001c0001t0002g0120others(8): Show | 11 | HG01109.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.565+40797_565+4079 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17417091 | |||||
| chrX:17417091
|
TACAC | T | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.565+40795_565+4079 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17417091 | |||||
| chrX:17417184
|
G | A | 1 | a0001c0001t0004g0058 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.565+40862G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17417184 | ||||||
| chrX:17417394
|
AT | A | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+41076delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17417394 | |||||
| chrX:17417786
|
T | G | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.565+41464T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17417786 | ||||||
| chrX:17418999
|
T | C | 1 | a0004c0005t0003g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.565+42677T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17418999 | ||||||
| chrX:17419203
|
C | T | 41 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0127others(38): Show | 41 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.565+42881C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17419203 | ||||||
| chrX:17419232
|
C | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+42910C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17419232 | ||||||
| chrX:17419450
|
T | G | 1 | a0001c0001t0002g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.565+43128T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17419450 | ||||||
| chrX:17419554
|
A | G | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+43232A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17419554 | ||||||
| chrX:17419701
|
C | T | 1 | a0001c0001t0004g0058 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.565+43379C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17419701 | ||||||
| chrX:17419771
|
T | C | 2 | a0001c0001t0013g0059a0002c0002t0001g0105 | 2 | NA18965.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.565+43449T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17419771 | ||||||
| chrX:17419886
|
C | G | 1 | a0002c0002t0001g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.565+43564C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17419886 | ||||||
| chrX:17420024
|
G | T | 1 | a0002c0002t0001g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.565+43702G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17420024 | ||||||
| chrX:17420194
|
G | A | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+43872G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17420194 | ||||||
| chrX:17420376
|
A | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0061a0001c0001t0001g0090others(2): Show | 5 | NA18960.hp1 NA18967.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+44054A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17420376 | ||||||
| chrX:17420598
|
C | G | 10 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(7): Show | 10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+44276C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17420598 | ||||||
| chrX:17420691
|
C | T | 19 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(16): Show | 19 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.565+44369C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17420691 | ||||||
| chrX:17420802
|
A | G | 1 | a0002c0002t0001g0082 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.565+44480A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17420802 | ||||||
| chrX:17420904
|
TCTTA | T | 1 | a0002c0002t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.565+44587_565+4459 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17420904 | |||||
| chrX:17421067
|
C | CT | 1 | a0001c0001t0002g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.565+44755dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17421067 | |||||
| chrX:17421067
|
CT | C | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+44755delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17421067 | |||||
| chrX:17421226
|
C | CGT | 1 | a0004c0005t0003g0136 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.565+44922_565+4492 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17421226 | |||||
| chrX:17421266
|
C | CAT | 22 | a0001c0001t0002g0099a0001c0001t0002g0116a0001c0001t0002g0120others(19): Show | 22 | HG01106.hp1 HG01243.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.565+44944_565+4494 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17421266 | ||||||
| chrX:17421267
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.565+44945G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17421267 | ||||||
| chrX:17421408
|
T | TG | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+45087dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17421408 | |||||
| chrX:17421422
|
GA | G | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+45103delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17421422 | |||||
| chrX:17421725
|
C | T | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.565+45403C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17421725 | ||||||
| chrX:17421819
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0005g0103 | 3 | HG03139.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.565+45497C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17421819 | ||||||
| chrX:17421869
|
GC | G | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+45550delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17421869 | |||||
| chrX:17421911
|
CA | C | 1 | a0001c0001t0001g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.565+45595delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17421911 | |||||
| chrX:17421930
|
GACAT | G | 33 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0127others(30): Show | 33 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.565+45612_565+4561 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17421930 | |||||
| chrX:17422086
|
G | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0144 | 3 | NA18994.hp1 NA18995.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.565+45764G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17422086 | ||||||
| chrX:17422216
|
AT | A | 1 | a0001c0003t0002g0155 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.565+45896delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17422216 | |||||
| chrX:17422437
|
C | A | 3 | a0001c0001t0002g0121a0001c0001t0006g0112a0004c0005t0003g0117 | 3 | HG02280.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.565+46115C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17422437 | ||||||
| chrX:17422468
|
G | A | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+46146G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17422468 | ||||||
| chrX:17422512
|
G | C | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+46190G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17422512 | ||||||
| chrX:17422540
|
G | A | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+46218G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17422540 | ||||||
| chrX:17422675
|
A | AG | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+46355dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17422675 | |||||
| chrX:17422704
|
T | TG | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+46383dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17422704 | |||||
| chrX:17422968
|
GA | G | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+46650delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17422968 | |||||
| chrX:17423050
|
G | A | 2 | a0002c0002t0001g0078a0002c0002t0014g0063 | 2 | HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.565+46728G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17423050 | ||||||
| chrX:17423128
|
G | A | 1 | a0002c0002t0001g0080 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.565+46806G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17423128 | ||||||
| chrX:17423295
|
CTGTCT | C | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+46975_565+4697 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17423295 | |||||
| chrX:17423301
|
T | A | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+46979T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17423301 | ||||||
| chrX:17423446
|
A | G | 10 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(7): Show | 10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+47124A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17423446 | ||||||
| chrX:17423559
|
G | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+47237G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17423559 | ||||||
| chrX:17424317
|
C | T | 10 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(7): Show | 10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+47995C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17424317 | ||||||
| chrX:17424371
|
A | G | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+48049A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17424371 | ||||||
| chrX:17424697
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.565+48375A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17424697 | ||||||
| chrX:17425115
|
C | T | 22 | a0001c0001t0002g0099a0001c0001t0002g0116a0001c0001t0002g0120others(19): Show | 22 | HG01106.hp1 HG01243.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.565+48793C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17425115 | ||||||
| chrX:17425492
|
T | TGCTG | 51 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(48): Show | 51 | HG00609.hp1 HG01358.hp1 HG02015.hp1 others(48): Show |
intron_variant | MODIFIER | c.565+49171_565+4917 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425492 | |||||
| chrX:17425522
|
C | CA | 1 | a0011c0013t0001g0039 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.565+49249dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CA | C | 17 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0038others(14): Show | 17 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.565+49249delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAA | C | 11 | a0001c0001t0001g0135a0001c0001t0001g0140a0001c0001t0001g0145others(8): Show | 11 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.565+49248_565+4924 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAA | C | 6 | a0001c0001t0001g0022a0001c0001t0002g0085a0001c0001t0017g0154others(3): Show | 6 | HG01975.hp1 HG02083.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+49247_565+4924 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAAA | C | 5 | a0001c0001t0001g0098a0002c0002t0001g0008a0002c0002t0001g0016others(2): Show | 5 | HG01192.hp1 HG01515.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+49246_565+4924 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAAAA | C | 17 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0061others(14): Show | 17 | HG01099.hp1 HG01109.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.565+49245_565+4924 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAAAAA | C | 10 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0095others(7): Show | 10 | HG00408.hp2 HG01074.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+49244_565+4924 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAAAAAA | C | 2 | a0001c0003t0002g0155a0002c0002t0001g0003 | 2 | HG03041.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.565+49243_565+4924 others(11): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAAAAAA others(1): Show |
C | 1 | a0001c0003t0002g0019 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.565+49242_565+4924 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAAAAAA others(2): Show |
C | 1 | a0002c0002t0011g0020 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.565+49241_565+4924 others(13): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0002g0106a0001c0001t0002g0110 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+49237_565+4924 others(17): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAAAAAA others(8): Show |
C | 2 | a0002c0002t0001g0007a0009c0011t0002g0147 | 2 | HG02257.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.565+49235_565+4924 others(19): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0002g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.565+49233_565+4924 others(21): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+49231_565+4924 others(23): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAAAAAA others(13): Show |
C | 11 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(8): Show | 11 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.565+49230_565+4924 others(24): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAAAAAA others(14): Show |
C | 2 | a0001c0001t0002g0002a0001c0001t0004g0163 | 2 | HG01261.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.565+49229_565+4924 others(25): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAAAAAA others(15): Show |
C | 1 | a0002c0002t0001g0042 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.565+49228_565+4924 others(26): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAAAAAA others(16): Show |
C | 1 | a0001c0003t0002g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.565+49227_565+4924 others(27): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAAAAAA others(17): Show |
C | 9 | a0001c0001t0002g0146a0001c0001t0005g0111a0001c0003t0002g0101others(6): Show | 9 | HG01106.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.565+49226_565+4924 others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAAAAAA others(18): Show |
C | 1 | a0002c0002t0001g0021 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.565+49225_565+4924 others(29): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAAAAAA others(20): Show |
C | 3 | a0001c0001t0004g0058a0002c0002t0001g0087a0002c0002t0001g0088 | 3 | NA18945.hp1 NA18970.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.565+49223_565+4924 others(31): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAAAAAA others(21): Show |
C | 35 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(32): Show | 35 | HG00609.hp1 HG01358.hp1 HG02015.hp1 others(32): Show |
intron_variant | MODIFIER | c.565+49222_565+4924 others(32): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425522
|
CAAAAAAA others(22): Show |
C | 1 | a0003c0004t0001g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.565+49221_565+4924 others(33): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | |||||
| chrX:17425551
|
AAAAAAAA others(18): Show |
A | 1 | a0001c0001t0002g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.565+49233_565+4925 others(29): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425551 | |||||
| chrX:17425563
|
AAAAAAAA others(2): Show |
A | 1 | a0001c0001t0001g0133 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.565+49245_565+4925 others(13): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425563 | |||||
| chrX:17425563
|
AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0001g0012 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.565+49245_565+4926 others(21): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425563 | |||||
| chrX:17425564
|
A | G | 10 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(7): Show | 10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+49242A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17425564 | ||||||
| chrX:17425568
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+49249_565+4925 others(26): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425568 | |||||
| chrX:17425568
|
A | AAAAAAAA others(8): Show |
1 | a0004c0005t0003g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.565+49249_565+4925 others(19): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425568 | |||||
| chrX:17425568
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0001g0070 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.565+49249_565+4925 others(15): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425568 | |||||
| chrX:17425568
|
A | AAAAAAAG | 1 | a0001c0001t0002g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.565+49249_565+4925 others(11): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425568 | |||||
| chrX:17425568
|
A | AAAAAAG | 1 | a0001c0001t0001g0056 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.565+49249_565+4925 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425568 | |||||
| chrX:17425568
|
A | AAAAAG | 1 | a0002c0002t0001g0141 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.565+49249_565+4925 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425568 | |||||
| chrX:17425568
|
A | AAAG | 3 | a0001c0001t0001g0067a0001c0001t0001g0127a0001c0001t0009g0125 | 3 | HG02132.hp1 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.565+49248_565+4924 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425568 | |||||
| chrX:17425568
|
A | AAG | 1 | a0001c0001t0002g0126 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.565+49247_565+4924 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425568 | |||||
| chrX:17425568
|
A | AG | 1 | a0002c0002t0016g0005 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.565+49246_565+4924 others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17425568 | ||||||
| chrX:17425568
|
A | G | 105 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0038others(102): Show | 105 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.565+49246A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17425568 | ||||||
| chrX:17425616
|
A | G | 1 | a0002c0002t0001g0088 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.565+49294A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17425616 | ||||||
| chrX:17425939
|
G | A | 1 | a0001c0001t0017g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.565+49617G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17425939 | ||||||
| chrX:17426202
|
T | C | 1 | a0004c0005t0003g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.565+49880T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17426202 | ||||||
| chrX:17426457
|
T | C | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+50135T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17426457 | ||||||
| chrX:17426766
|
C | T | 10 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(7): Show | 10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+50444C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17426766 | ||||||
| chrX:17426769
|
G | C | 6 | a0001c0001t0001g0026a0002c0002t0001g0015a0002c0002t0001g0024others(3): Show | 6 | HG02083.hp1 NA18747.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+50447G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17426769 | ||||||
| chrX:17427422
|
T | C | 1 | a0002c0002t0001g0006 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.565+51100T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17427422 | ||||||
| chrX:17427743
|
A | T | 2 | a0002c0002t0001g0030a0003c0004t0001g0013 | 2 | HG01975.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.565+51421A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17427743 | ||||||
| chrX:17427796
|
T | TA | 2 | a0001c0001t0001g0127a0001c0001t0009g0125 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.565+51480dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17427796 | |||||
| chrX:17427860
|
A | G | 1 | a0001c0003t0002g0155 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.565+51538A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17427860 | ||||||
| chrX:17427922
|
C | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+51600C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17427922 | ||||||
| chrX:17427943
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.565+51621C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17427943 | ||||||
| chrX:17428142
|
G | A | 22 | a0001c0001t0002g0099a0001c0001t0002g0116a0001c0001t0002g0120others(19): Show | 22 | HG01106.hp1 HG01243.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.565+51820G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17428142 | ||||||
| chrX:17428579
|
A | G | 1 | a0001c0001t0006g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.565+52257A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17428579 | ||||||
| chrX:17428850
|
C | G | 4 | a0001c0001t0001g0022a0001c0001t0002g0099a0001c0001t0002g0146others(1): Show | 4 | HG01243.hp1 HG02135.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+52528C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17428850 | ||||||
| chrX:17428908
|
T | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+52586T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17428908 | ||||||
| chrX:17428996
|
C | T | 5 | a0006c0007t0002g0115a0006c0007t0002g0118a0006c0008t0001g0114others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+52674C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17428996 | ||||||
| chrX:17429224
|
A | ATG | 4 | a0001c0001t0001g0041a0001c0001t0001g0137a0002c0002t0001g0016others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+52935_565+5293 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17429224 | |||||
| chrX:17429224
|
A | ATGTGTG | 1 | a0002c0002t0006g0060 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.565+52931_565+5293 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17429224 | |||||
| chrX:17429224
|
A | ATGTGTGT others(1): Show |
1 | a0004c0005t0003g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.565+52929_565+5293 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17429224 | |||||
| chrX:17429224
|
ATG | A | 42 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(39): Show | 42 | HG00609.hp1 HG01358.hp1 HG02015.hp1 others(39): Show |
intron_variant | MODIFIER | c.565+52935_565+5293 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17429224 | |||||
| chrX:17429224
|
ATGTG | A | 7 | a0002c0002t0001g0032a0002c0002t0001g0071a0002c0002t0001g0072others(4): Show | 7 | HG01099.hp1 HG02129.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+52933_565+5293 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17429224 | |||||
| chrX:17429239
|
T | TGTGTGTG others(3): Show |
3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+52926_565+5292 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17429239 | |||||
| chrX:17429257
|
T | C | 3 | a0001c0001t0001g0140a0001c0001t0001g0145a0002c0002t0001g0123 | 3 | HG00639.hp1 HG00639.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.565+52935T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17429257 | ||||||
| chrX:17429257
|
T | TGC | 2 | a0001c0001t0002g0116a0001c0001t0002g0120 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.565+52936_565+5293 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17429257 | |||||
| chrX:17429257
|
T | TGTGC | 7 | a0001c0001t0002g0121a0001c0001t0006g0112a0004c0005t0003g0117others(4): Show | 7 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.565+52936_565+5293 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17429257 | |||||
| chrX:17429257
|
T | TGTGTGC | 1 | a0006c0008t0008g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.565+52936_565+5293 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17429257 | |||||
| chrX:17429257
|
T | TGTGTGTG others(1): Show |
3 | a0001c0001t0005g0111a0001c0003t0002g0101a0005c0006t0008g0161 | 3 | HG02922.hp2 HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.565+52936_565+5293 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17429257 | |||||
| chrX:17429257
|
T | TGTGTGTG others(3): Show |
6 | a0001c0003t0002g0128a0005c0006t0001g0157a0005c0006t0001g0162others(3): Show | 6 | HG01106.hp1 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+52936_565+5293 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17429257 | |||||
| chrX:17429265
|
T | C | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+52943T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17429265 | ||||||
| chrX:17429608
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.565+53286C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17429608 | ||||||
| chrX:17429855
|
G | A | 1 | a0002c0002t0001g0008 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.565+53533G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17429855 | ||||||
| chrX:17430005
|
C | G | 127 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0041others(124): Show | 127 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.565+53683C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430005 | ||||||
| chrX:17430075
|
T | TTTCC | 28 | a0001c0001t0001g0104a0001c0001t0001g0127a0001c0001t0002g0126others(25): Show | 28 | HG01071.hp1 HG01928.hp1 HG01975.hp1 others(25): Show |
intron_variant | MODIFIER | c.565+53792_565+5379 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430075 | |||||
| chrX:17430075
|
T | TTTCCTTC others(1): Show |
2 | a0001c0001t0002g0099a0001c0001t0009g0122 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.565+53788_565+5379 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430075 | |||||
| chrX:17430075
|
T | TTTCCTTC others(9): Show |
1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.565+53780_565+5379 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430075 | |||||
| chrX:17430075
|
TTTCC | T | 10 | a0001c0001t0001g0081a0001c0001t0001g0151a0001c0001t0005g0111others(7): Show | 10 | HG00408.hp1 HG01106.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+53792_565+5379 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430075 | |||||
| chrX:17430075
|
TTTCCTTC others(5): Show |
T | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.565+53784_565+5379 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430075 | |||||
| chrX:17430075
|
TTTCCTTC others(9): Show |
T | 1 | a0001c0003t0002g0019 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.565+53780_565+5379 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430075 | |||||
| chrX:17430151
|
C | CCTT | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+53833_565+5383 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430151 | |||||
| chrX:17430230
|
TTCCCTCC others(1): Show |
T | 3 | a0001c0001t0001g0061a0001c0001t0001g0090a0001c0001t0001g0098 | 3 | NA18967.hp1 NA18983.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.565+53921_565+5392 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430230 | |||||
| chrX:17430257
|
CTT | C | 2 | a0002c0002t0001g0011a0002c0002t0001g0033 | 2 | HG01192.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.565+53939_565+5394 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430257 | |||||
| chrX:17430259
|
T | TCTTTC | 1 | a0002c0002t0001g0015 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.565+53937_565+5393 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430259 | ||||||
| chrX:17430259
|
T | TTCTTTC | 1 | a0001c0001t0002g0126 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.565+53938_565+5393 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | |||||
| chrX:17430259
|
T | TTTC | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+53939_565+5394 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | |||||
| chrX:17430259
|
T | TTTCTTTC | 1 | a0002c0002t0001g0024 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.565+53939_565+5394 others(11): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | |||||
| chrX:17430259
|
T | TTTTC | 21 | a0001c0001t0001g0029a0001c0001t0001g0041a0001c0001t0001g0137others(18): Show | 21 | HG00642.hp1 HG01099.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.565+53990_565+5399 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | |||||
| chrX:17430259
|
T | TTTTCTTT others(1): Show |
10 | a0001c0001t0001g0081a0001c0001t0001g0094a0001c0001t0001g0124others(7): Show | 10 | HG00280.hp1 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+53986_565+5399 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | |||||
| chrX:17430259
|
T | TTTTCTTT others(5): Show |
9 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(6): Show | 9 | HG01258.hp1 HG01433.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.565+53982_565+5399 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | |||||
| chrX:17430259
|
T | TTTTCTTT others(9): Show |
1 | a0002c0002t0001g0031 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.565+53978_565+5399 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | |||||
| chrX:17430259
|
TTTTC | T | 42 | a0001c0001t0001g0026a0001c0001t0001g0049a0001c0001t0001g0050others(39): Show | 42 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.565+53990_565+5399 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | |||||
| chrX:17430259
|
TTTTCTTT others(1): Show |
T | 33 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0048others(30): Show | 33 | HG00408.hp1 HG01106.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.565+53986_565+5399 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | |||||
| chrX:17430259
|
TTTTCTTT others(5): Show |
T | 10 | a0001c0001t0001g0083a0001c0001t0001g0104a0001c0001t0002g0121others(7): Show | 10 | HG00621.hp1 HG02040.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+53982_565+5399 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | |||||
| chrX:17430259
|
TTTTCTTT others(9): Show |
T | 4 | a0002c0002t0001g0082a0002c0002t0001g0109a0002c0002t0001g0138others(1): Show | 4 | HG00673.hp1 HG02074.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+53978_565+5399 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | |||||
| chrX:17430259
|
TTTTCTTT others(17): Show |
T | 1 | a0001c0001t0002g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.565+53970_565+5399 others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | |||||
| chrX:17430269
|
T | C | 1 | a0002c0002t0001g0075 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.565+53947T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430269 | ||||||
| chrX:17430283
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.565+53961C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430283 | ||||||
| chrX:17430311
|
CTTTCCTT others(1): Show |
C | 1 | a0001c0003t0002g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.565+53990_565+5399 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430311 | ||||||
| chrX:17430315
|
C | CTTTCTTT | 1 | a0005c0006t0001g0162 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.565+53993_565+5399 others(11): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430315 | ||||||
| chrX:17430316
|
C | T | 1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.565+53994C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430316 | ||||||
| chrX:17430319
|
T | C | 1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.565+53997T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430319 | ||||||
| chrX:17430319
|
T | TC | 1 | a0005c0006t0001g0162 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.565+53998dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430319 | |||||
| chrX:17430325
|
TTTC | T | 2 | a0001c0001t0002g0099a0001c0001t0002g0146 | 2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.565+54006_565+5400 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430325 | |||||
| chrX:17430328
|
C | CT | 1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.565+54011dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430328 | |||||
| chrX:17430337
|
CTCTT | C | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0005g0103 | 3 | HG03139.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.565+54029_565+5403 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430337 | |||||
| chrX:17430355
|
T | C | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+54033T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430355 | ||||||
| chrX:17430357
|
C | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+54035C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430357 | ||||||
| chrX:17430360
|
C | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+54038C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430360 | ||||||
| chrX:17430361
|
T | C | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+54039T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430361 | ||||||
| chrX:17430410
|
C | CTCCT | 4 | a0001c0001t0002g0099a0001c0001t0002g0146a0001c0001t0009g0125others(1): Show | 4 | HG01243.hp1 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+54106_565+5410 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430410 | |||||
| chrX:17430870
|
T | A | 1 | a0001c0001t0001g0081 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.565+54548T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430870 | ||||||
| chrX:17431023
|
T | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0145a0002c0002t0001g0123 | 3 | HG00639.hp1 HG00639.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.565+54701T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17431023 | ||||||
| chrX:17431888
|
T | C | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+55566T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17431888 | ||||||
| chrX:17432152
|
C | G | 1 | a0001c0001t0001g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.565+55830C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17432152 | ||||||
| chrX:17432219
|
A | AG | 4 | a0001c0001t0001g0061a0001c0001t0001g0090a0001c0001t0001g0098others(1): Show | 4 | NA18967.hp1 NA18983.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+55899dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17432219 | |||||
| chrX:17432444
|
A | G | 2 | a0001c0001t0005g0111a0001c0003t0002g0101 | 2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.565+56122A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17432444 | ||||||
| chrX:17432848
|
A | T | 9 | a0001c0001t0005g0111a0001c0003t0002g0101a0001c0003t0002g0128others(6): Show | 9 | HG01106.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+56526A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17432848 | ||||||
| chrX:17432885
|
G | A | 19 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(16): Show | 19 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.565+56563G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17432885 | ||||||
| chrX:17432901
|
G | A | 1 | a0002c0002t0001g0017 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.565+56579G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17432901 | ||||||
| chrX:17432930
|
G | A | 1 | a0002c0002t0001g0040 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.565+56608G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17432930 | ||||||
| chrX:17433032
|
T | TC | 1 | a0011c0013t0001g0039 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.565+56715dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17433032 | |||||
| chrX:17433036
|
C | T | 38 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(35): Show | 38 | HG00609.hp1 HG01358.hp1 HG02015.hp1 others(35): Show |
intron_variant | MODIFIER | c.565+56714C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433036 | ||||||
| chrX:17433105
|
C | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+56783C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433105 | ||||||
| chrX:17433115
|
T | C | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.565+56793T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433115 | ||||||
| chrX:17433116
|
C | G | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.565+56794C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433116 | ||||||
| chrX:17433123
|
A | G | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.565+56801A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433123 | ||||||
| chrX:17433130
|
C | T | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.565+56808C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433130 | ||||||
| chrX:17433142
|
G | A | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.565+56820G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433142 | ||||||
| chrX:17433184
|
C | G | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.565+56862C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433184 | ||||||
| chrX:17433196
|
C | CT | 30 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0056others(27): Show | 30 | HG00609.hp1 HG00621.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.565+56900dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17433196 | |||||
| chrX:17433196
|
CT | C | 4 | a0002c0002t0001g0045a0002c0002t0001g0076a0002c0002t0001g0156others(1): Show | 4 | HG00140.hp1 HG02965.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+56900delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17433196 | |||||
| chrX:17433196
|
CTTTT | C | 2 | a0001c0001t0002g0116a0006c0008t0008g0113 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.565+56897_565+5690 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17433196 | |||||
| chrX:17433196
|
CTTTTT | C | 17 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0005g0111others(14): Show | 17 | HG01106.hp1 HG02280.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.565+56896_565+5690 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17433196 | |||||
| chrX:17433196
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+56891_565+5690 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17433196 | |||||
| chrX:17433196
|
CTTTTTTT others(6): Show |
C | 1 | a0003c0004t0001g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.565+56888_565+5690 others(17): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17433196 | |||||
| chrX:17433282
|
A | C | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.565+56960A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433282 | ||||||
| chrX:17433284
|
T | C | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.565+56962T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433284 | ||||||
| chrX:17433291
|
T | C | 160 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(157): Show | 160 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.565+56969T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433291 | ||||||
| chrX:17433552
|
C | T | 1 | a0002c0002t0014g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.565+57230C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433552 | ||||||
| chrX:17433891
|
A | T | 9 | a0001c0001t0005g0111a0001c0003t0002g0101a0001c0003t0002g0128others(6): Show | 9 | HG01106.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+57569A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433891 | ||||||
| chrX:17433928
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.565+57606T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433928 | ||||||
| chrX:17434169
|
T | C | 1 | a0001c0001t0002g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.565+57847T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17434169 | ||||||
| chrX:17434313
|
A | C | 1 | a0001c0001t0002g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.565+57991A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17434313 | ||||||
| chrX:17434441
|
A | AT | 22 | a0001c0001t0001g0029a0001c0001t0001g0090a0001c0001t0002g0002others(19): Show | 22 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.565+58140dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17434441 | |||||
| chrX:17434441
|
A | ATT | 2 | a0001c0001t0002g0120a0009c0011t0002g0147 | 2 | HG02257.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.565+58139_565+5814 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17434441 | |||||
| chrX:17434441
|
AT | A | 28 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0129others(25): Show | 28 | HG00408.hp1 HG00621.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.565+58140delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17434441 | |||||
| chrX:17434441
|
ATT | A | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.565+58139_565+5814 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17434441 | |||||
| chrX:17434442
|
T | TC | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+58120_565+5812 others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17434442 | ||||||
| chrX:17434515
|
T | C | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+58193T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17434515 | ||||||
| chrX:17434594
|
C | T | 9 | a0001c0001t0005g0111a0001c0003t0002g0101a0001c0003t0002g0128others(6): Show | 9 | HG01106.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+58272C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17434594 | ||||||
| chrX:17436130
|
G | GT | 1 | a0001c0001t0001g0050 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.565+59815dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17436130 | |||||
| chrX:17436132
|
T | G | 1 | a0002c0002t0001g0014 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.565+59810T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17436132 | ||||||
| chrX:17436612
|
T | TA | 9 | a0001c0001t0005g0111a0001c0003t0002g0101a0001c0003t0002g0128others(6): Show | 9 | HG01106.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+60306dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17436612 | |||||
| chrX:17436612
|
TA | T | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0002g0099others(5): Show | 8 | HG01243.hp1 HG02257.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.565+60306delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17436612 | |||||
| chrX:17436624
|
A | G | 1 | a0002c0002t0001g0023 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.565+60302A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17436624 | ||||||
| chrX:17436907
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.565+60585A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17436907 | ||||||
| chrX:17437156
|
G | A | 1 | a0001c0003t0002g0019 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.565+60834G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17437156 | ||||||
| chrX:17437248
|
C | G | 13 | a0001c0001t0002g0099a0001c0001t0002g0116a0001c0001t0002g0120others(10): Show | 13 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.565+60926C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17437248 | ||||||
| chrX:17437673
|
T | C | 1 | a0005c0006t0008g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565+61351T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17437673 | ||||||
| chrX:17439178
|
A | T | 163 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(160): Show | 163 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.565+62856A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17439178 | ||||||
| chrX:17439578
|
A | G | 1 | a0005c0006t0008g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565+63256A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17439578 | ||||||
| chrX:17439767
|
A | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+63445A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17439767 | ||||||
| chrX:17440258
|
T | TA | 25 | a0001c0001t0001g0070a0001c0001t0001g0081a0001c0001t0001g0133others(22): Show | 25 | HG01358.hp1 HG01928.hp1 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.565+63963dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17440258 | |||||
| chrX:17440258
|
T | TAA | 1 | a0006c0008t0008g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.565+63962_565+6396 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17440258 | |||||
| chrX:17440258
|
T | TAAA | 1 | a0001c0001t0002g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.565+63961_565+6396 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17440258 | |||||
| chrX:17440258
|
T | TAAAA | 2 | a0001c0001t0002g0146a0009c0011t0002g0147 | 2 | HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+63960_565+6396 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17440258 | |||||
| chrX:17440258
|
TA | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0038a0001c0001t0001g0083others(5): Show | 8 | HG01167.hp1 HG02040.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.565+63963delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17440258 | |||||
| chrX:17440396
|
G | C | 1 | a0005c0006t0008g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565+64074G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17440396 | ||||||
| chrX:17440618
|
A | G | 5 | a0001c0001t0002g0004a0001c0001t0002g0093a0001c0001t0002g0096others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+64296A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17440618 | ||||||
| chrX:17440733
|
G | A | 1 | a0002c0002t0016g0005 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.565+64411G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17440733 | ||||||
| chrX:17441153
|
G | A | 1 | a0004c0005t0003g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.565+64831G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17441153 | ||||||
| chrX:17441654
|
T | TTTCC | 1 | a0002c0002t0001g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.565+65352_565+6535 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17441654 | |||||
| chrX:17441666
|
CTTCCTTC others(5): Show |
C | 3 | a0005c0006t0001g0157a0005c0006t0005g0159a0008c0010t0003g0158 | 3 | HG01106.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.565+65356_565+6536 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17441666 | |||||
| chrX:17441673
|
C | T | 2 | a0002c0002t0001g0021a0002c0015t0001g0046 | 2 | HG00280.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.565+65351C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17441673 | ||||||
| chrX:17441958
|
A | G | 1 | a0002c0002t0001g0021 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.565+65636A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17441958 | ||||||
| chrX:17442339
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+66017A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17442339 | ||||||
| chrX:17442703
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.565+66381G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17442703 | ||||||
| chrX:17443230
|
C | T | 1 | a0005c0006t0008g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565+66908C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17443230 | ||||||
| chrX:17443255
|
G | A | 1 | a0002c0002t0001g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.565+66933G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17443255 | ||||||
| chrX:17443453
|
G | A | 13 | a0001c0001t0002g0099a0001c0001t0002g0116a0001c0001t0002g0120others(10): Show | 13 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.565+67131G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17443453 | ||||||
| chrX:17443614
|
G | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+67292G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17443614 | ||||||
| chrX:17443722
|
G | A | 2 | a0001c0001t0005g0111a0001c0003t0002g0101 | 2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.565+67400G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17443722 | ||||||
| chrX:17444253
|
G | T | 1 | a0002c0002t0001g0064 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.565+67931G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17444253 | ||||||
| chrX:17444311
|
G | C | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+67989G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17444311 | ||||||
| chrX:17444634
|
A | G | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+68312A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17444634 | ||||||
| chrX:17444704
|
C | T | 1 | a0002c0002t0001g0014 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.565+68382C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17444704 | ||||||
| chrX:17444870
|
A | AT | 2 | a0001c0001t0002g0146a0009c0011t0002g0147 | 2 | HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+68559dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17444870 | |||||
| chrX:17444910
|
GT | G | 1 | a0002c0002t0001g0042 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.565+68593delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17444910 | |||||
| chrX:17445069
|
C | T | 1 | a0003c0004t0001g0055 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.565+68747C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17445069 | ||||||
| chrX:17445756
|
A | AG | 13 | a0001c0001t0001g0098a0001c0001t0002g0120a0001c0001t0002g0121others(10): Show | 13 | HG00621.hp1 HG01099.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.565+69444dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17445756 | |||||
| chrX:17445756
|
A | AGG | 2 | a0001c0001t0002g0116a0002c0002t0001g0108 | 2 | HG03209.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.565+69443_565+6944 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17445756 | |||||
| chrX:17445756
|
A | G | 1 | a0001c0001t0004g0058 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.565+69434A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17445756 | ||||||
| chrX:17445756
|
AG | A | 1 | a0002c0002t0001g0006 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.565+69444delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17445756 | |||||
| chrX:17445758
|
G | C | 1 | a0002c0002t0001g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.565+69436G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17445758 | ||||||
| chrX:17445837
|
T | TA | 1 | a0004c0005t0003g0136 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.565+69531dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17445837 | |||||
| chrX:17445837
|
TA | T | 5 | a0001c0001t0001g0124a0001c0001t0002g0099a0001c0001t0002g0146others(2): Show | 5 | HG01243.hp1 HG01943.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+69531delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17445837 | |||||
| chrX:17445851
|
A | C | 1 | a0001c0001t0001g0022 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.565+69529A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17445851 | ||||||
| chrX:17445890
|
C | G | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+69568C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17445890 | ||||||
| chrX:17445963
|
A | T | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+69641A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17445963 | ||||||
| chrX:17445991
|
C | G | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+69669C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17445991 | ||||||
| chrX:17446169
|
G | A | 1 | a0002c0002t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.565+69847G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17446169 | ||||||
| chrX:17446552
|
C | T | 4 | a0001c0001t0001g0127a0001c0001t0002g0126a0001c0001t0009g0125others(1): Show | 4 | HG01071.hp1 HG02647.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+70230C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17446552 | ||||||
| chrX:17446647
|
C | CT | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+70330dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17446647 | |||||
| chrX:17446656
|
C | CA | 8 | a0001c0001t0001g0061a0001c0001t0001g0090a0001c0001t0001g0098others(5): Show | 8 | HG00140.hp1 HG01934.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.565+70349dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17446656 | |||||
| chrX:17446656
|
C | CAA | 1 | a0002c0002t0001g0071 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.565+70348_565+7034 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17446656 | |||||
| chrX:17446656
|
CA | C | 14 | a0001c0001t0001g0151a0001c0001t0002g0099a0001c0001t0002g0116others(11): Show | 14 | HG00408.hp1 HG01243.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.565+70349delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17446656 | |||||
| chrX:17446656
|
CAA | C | 1 | a0001c0001t0006g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.565+70348_565+7034 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17446656 | |||||
| chrX:17447114
|
T | G | 1 | a0011c0013t0001g0039 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.565+70792T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17447114 | ||||||
| chrX:17447165
|
T | C | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+70843T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17447165 | ||||||
| chrX:17447396
|
A | AT | 7 | a0001c0001t0001g0098a0001c0001t0001g0127a0001c0001t0002g0126others(4): Show | 7 | HG01071.hp1 HG02257.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+71084dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447396 | |||||
| chrX:17447396
|
A | ATT | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+71083_565+7108 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447396 | |||||
| chrX:17447396
|
AT | A | 4 | a0005c0006t0001g0157a0005c0006t0005g0159a0007c0009t0002g0160others(1): Show | 4 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+71084delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447396 | |||||
| chrX:17447755
|
C | CCA | 1 | a0002c0002t0001g0025 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.565+71449_565+7145 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447755 | |||||
| chrX:17447773
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.565+71451G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17447773 | ||||||
| chrX:17447773
|
GCA | G | 1 | a0002c0002t0016g0005 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.565+71461_565+7146 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447773 | |||||
| chrX:17447773
|
GCACACAC others(19): Show |
G | 1 | a0002c0002t0001g0023 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.565+71463_565+7148 others(30): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447773 | |||||
| chrX:17447775
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.565+71453A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17447775 | ||||||
| chrX:17447785
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.565+71463G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17447785 | ||||||
| chrX:17447785
|
G | GCA | 13 | a0001c0001t0001g0041a0001c0001t0002g0002a0001c0001t0002g0085others(10): Show | 13 | HG00140.hp1 HG01071.hp1 HG02293.hp2 others(10): Show |
intron_variant | MODIFIER | c.565+71496_565+7149 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447785 | |||||
| chrX:17447785
|
G | GCACA | 6 | a0001c0001t0001g0070a0001c0001t0002g0043a0004c0005t0003g0100others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+71494_565+7149 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447785 | |||||
| chrX:17447785
|
G | GCACACA | 6 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+71492_565+7149 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447785 | |||||
| chrX:17447785
|
G | GCACACAC others(3): Show |
1 | a0001c0001t0006g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.565+71488_565+7149 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447785 | |||||
| chrX:17447785
|
GCA | G | 43 | a0001c0001t0001g0029a0001c0001t0001g0048a0001c0001t0001g0049others(40): Show | 43 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.565+71496_565+7149 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447785 | |||||
| chrX:17447785
|
GCACA | G | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+71494_565+7149 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447785 | |||||
| chrX:17447785
|
GCACACA | G | 2 | a0002c0002t0001g0071a0002c0002t0001g0084 | 2 | HG02015.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.565+71492_565+7149 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447785 | |||||
| chrX:17447785
|
GCACACAC others(1): Show |
G | 1 | a0002c0002t0001g0076 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.565+71490_565+7149 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447785 | |||||
| chrX:17447787
|
A | G | 3 | a0001c0001t0001g0068a0001c0001t0017g0154a0002c0002t0001g0007 | 3 | HG01975.hp1 HG03130.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.565+71465A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17447787 | ||||||
| chrX:17447820
|
G | C | 2 | a0002c0002t0001g0138a0002c0002t0001g0139 | 2 | HG00673.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.565+71498G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17447820 | ||||||
| chrX:17447935
|
A | G | 1 | a0002c0002t0001g0078 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.565+71613A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17447935 | ||||||
| chrX:17447977
|
C | G | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.565+71655C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17447977 | ||||||
| chrX:17448138
|
G | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+71816G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17448138 | ||||||
| chrX:17449252
|
G | A | 1 | a0008c0010t0003g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.565+72930G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17449252 | ||||||
| chrX:17449585
|
G | T | 1 | a0001c0003t0002g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.565+73263G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17449585 | ||||||
| chrX:17449797
|
C | T | 9 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(6): Show | 9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.565+73475C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17449797 | ||||||
| chrX:17450509
|
GT | G | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+74189delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17450509 | |||||
| chrX:17450642
|
G | A | 10 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(7): Show | 10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+74320G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17450642 | ||||||
| chrX:17451058
|
A | ATACT | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+74738_565+7473 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17451058 | |||||
| chrX:17451157
|
T | C | 1 | a0001c0001t0001g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.565+74835T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17451157 | ||||||
| chrX:17451252
|
T | C | 4 | a0001c0001t0001g0068a0001c0001t0002g0106a0001c0001t0002g0107others(1): Show | 4 | HG02258.hp1 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+74930T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17451252 | ||||||
| chrX:17451621
|
G | A | 14 | a0001c0001t0002g0099a0001c0001t0002g0116a0001c0001t0002g0120others(11): Show | 14 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.565+75299G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17451621 | ||||||
| chrX:17452131
|
C | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+75809C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17452131 | ||||||
| chrX:17452278
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.565+75956G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17452278 | ||||||
| chrX:17452418
|
C | T | 1 | a0005c0006t0001g0162 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.565+76096C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17452418 | ||||||
| chrX:17452440
|
A | G | 1 | a0002c0002t0001g0025 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.565+76118A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17452440 | ||||||
| chrX:17452484
|
T | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+76162T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17452484 | ||||||
| chrX:17452491
|
G | GT | 4 | a0001c0001t0002g0099a0001c0001t0002g0146a0002c0002t0001g0075others(1): Show | 4 | HG01243.hp1 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+76181dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17452491 | |||||
| chrX:17452491
|
GT | G | 3 | a0001c0001t0005g0111a0001c0001t0007g0073a0001c0003t0002g0101 | 3 | HG02922.hp2 NA18906.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.565+76181delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17452491 | |||||
| chrX:17452498
|
T | G | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0005g0103 | 3 | HG03139.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.565+76176T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17452498 | ||||||
| chrX:17452498
|
T | TG | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+76176_565+7617 others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17452498 | ||||||
| chrX:17452665
|
A | T | 7 | a0001c0001t0002g0004a0001c0001t0002g0093a0001c0001t0002g0096others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+76343A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17452665 | ||||||
| chrX:17453074
|
A | G | 5 | a0006c0007t0002g0115a0006c0007t0002g0118a0006c0008t0001g0114others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+76752A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17453074 | ||||||
| chrX:17453185
|
T | C | 1 | a0005c0006t0001g0162 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.565+76863T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17453185 | ||||||
| chrX:17453546
|
A | G | 14 | a0001c0001t0002g0099a0001c0001t0002g0116a0001c0001t0002g0120others(11): Show | 14 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.565+77224A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17453546 | ||||||
| chrX:17453753
|
A | T | 4 | a0005c0006t0001g0157a0005c0006t0005g0159a0007c0009t0002g0160others(1): Show | 4 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+77431A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17453753 | ||||||
| chrX:17453781
|
A | G | 53 | a0001c0001t0001g0029a0001c0001t0001g0048a0001c0001t0001g0049others(50): Show | 53 | HG00609.hp1 HG01358.hp1 HG02015.hp1 others(50): Show |
intron_variant | MODIFIER | c.565+77459A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17453781 | ||||||
| chrX:17453815
|
G | T | 1 | a0002c0002t0001g0071 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.565+77493G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17453815 | ||||||
| chrX:17454663
|
C | A | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+78341C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17454663 | ||||||
| chrX:17454787
|
C | T | 1 | a0002c0002t0001g0064 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.565+78465C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17454787 | ||||||
| chrX:17455212
|
T | A | 1 | a0003c0004t0001g0132 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.565+78890T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17455212 | ||||||
| chrX:17455377
|
A | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+79055A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17455377 | ||||||
| chrX:17455453
|
A | T | 2 | a0001c0001t0005g0111a0001c0003t0002g0101 | 2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.565+79131A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17455453 | ||||||
| chrX:17455553
|
TAGA | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+79233_565+7923 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17455553 | |||||
| chrX:17455714
|
C | T | 10 | a0001c0001t0002g0099a0001c0001t0002g0146a0001c0003t0002g0128others(7): Show | 10 | HG01106.hp1 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+79392C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17455714 | ||||||
| chrX:17456155
|
G | T | 6 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0070others(3): Show | 6 | HG02132.hp1 HG02698.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+79833G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17456155 | ||||||
| chrX:17456248
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.565+79926A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17456248 | ||||||
| chrX:17456480
|
A | G | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.565+80158A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17456480 | ||||||
| chrX:17456861
|
T | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+80539T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17456861 | ||||||
| chrX:17457218
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.565+80896G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17457218 | ||||||
| chrX:17457420
|
AAG | A | 1 | a0001c0001t0017g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.565+81103_565+8110 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17457420 | |||||
| chrX:17457539
|
C | A | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+81217C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17457539 | ||||||
| chrX:17457912
|
A | G | 2 | a0001c0001t0005g0111a0001c0003t0002g0101 | 2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.565+81590A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17457912 | ||||||
| chrX:17458221
|
CTTTG | C | 4 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(1): Show | 4 | HG02258.hp1 HG03041.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+81919_565+8192 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17458221 | |||||
| chrX:17458452
|
C | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+82130C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17458452 | ||||||
| chrX:17458467
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+82145C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17458467 | ||||||
| chrX:17458481
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.565+82159G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17458481 | ||||||
| chrX:17458586
|
G | A | 1 | a0001c0001t0002g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.565+82264G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17458586 | ||||||
| chrX:17458674
|
T | G | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+82352T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17458674 | ||||||
| chrX:17458736
|
G | C | 4 | a0001c0001t0001g0026a0002c0002t0001g0015a0002c0002t0001g0053others(1): Show | 4 | HG02083.hp1 NA18747.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+82414G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17458736 | ||||||
| chrX:17459148
|
T | G | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+82826T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17459148 | ||||||
| chrX:17459346
|
C | A | 1 | a0002c0002t0001g0003 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.565+83024C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17459346 | ||||||
| chrX:17459941
|
A | G | 10 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(7): Show | 10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+83619A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17459941 | ||||||
| chrX:17460057
|
G | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+83735G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17460057 | ||||||
| chrX:17460192
|
A | G | 1 | a0001c0003t0002g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.565+83870A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17460192 | ||||||
| chrX:17460370
|
A | C | 14 | a0001c0001t0002g0099a0001c0001t0002g0116a0001c0001t0002g0120others(11): Show | 14 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.565+84048A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17460370 | ||||||
| chrX:17460420
|
A | AG | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+84100dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17460420 | |||||
| chrX:17460487
|
AT | A | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+84169delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17460487 | |||||
| chrX:17460509
|
A | AT | 1 | a0005c0006t0008g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565+84199dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17460509 | |||||
| chrX:17460614
|
C | T | 1 | a0013c0016t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.565+84292C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17460614 | ||||||
| chrX:17460628
|
A | C | 7 | a0001c0003t0002g0128a0005c0006t0001g0157a0005c0006t0001g0162others(4): Show | 7 | HG01106.hp1 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.565+84306A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17460628 | ||||||
| chrX:17460650
|
AT | A | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+84331delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17460650 | |||||
| chrX:17460712
|
G | A | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+84390G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17460712 | ||||||
| chrX:17461020
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.565+84698A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17461020 | ||||||
| chrX:17461035
|
AT | A | 10 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(7): Show | 10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+84715delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17461035 | |||||
| chrX:17461131
|
A | C | 1 | a0002c0002t0001g0040 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.565+84809A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17461131 | ||||||
| chrX:17461148
|
G | A | 20 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0129others(17): Show | 20 | HG00408.hp1 HG00621.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.565+84826G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17461148 | ||||||
| chrX:17461308
|
C | G | 1 | a0001c0001t0001g0009 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.565+84986C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17461308 | ||||||
| chrX:17462035
|
A | G | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+85713A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17462035 | ||||||
| chrX:17462072
|
T | C | 2 | a0001c0001t0005g0111a0001c0003t0002g0101 | 2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.565+85750T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17462072 | ||||||
| chrX:17462083
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.565+85761A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17462083 | ||||||
| chrX:17462806
|
T | C | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+86484T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17462806 | ||||||
| chrX:17462863
|
C | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+86541C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17462863 | ||||||
| chrX:17463262
|
G | A | 10 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(7): Show | 10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+86940G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17463262 | ||||||
| chrX:17463372
|
G | GT | 1 | a0002c0002t0001g0037 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.565+87061dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17463372 | |||||
| chrX:17463372
|
GT | G | 2 | a0001c0001t0001g0151a0001c0001t0002g0164 | 2 | HG00408.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.565+87061delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17463372 | |||||
| chrX:17463372
|
GTT | G | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+87060_565+8706 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17463372 | |||||
| chrX:17463515
|
A | G | 14 | a0001c0001t0002g0099a0001c0001t0002g0116a0001c0001t0002g0120others(11): Show | 14 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.565+87193A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17463515 | ||||||
| chrX:17463713
|
C | G | 1 | a0013c0016t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.565+87391C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17463713 | ||||||
| chrX:17463725
|
C | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+87403C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17463725 | ||||||
| chrX:17463946
|
G | T | 1 | a0002c0002t0001g0082 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.565+87624G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17463946 | ||||||
| chrX:17464095
|
G | GT | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+87777dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17464095 | |||||
| chrX:17464118
|
TG | T | 1 | a0002c0002t0001g0062 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.565+87801delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17464118 | |||||
| chrX:17464156
|
A | G | 1 | a0002c0002t0001g0003 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.565+87834A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17464156 | ||||||
| chrX:17464787
|
A | G | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0005g0103 | 3 | HG03139.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.565+88465A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17464787 | ||||||
| chrX:17465038
|
G | A | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+88716G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17465038 | ||||||
| chrX:17465122
|
C | A | 1 | a0001c0001t0002g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.565+88800C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17465122 | ||||||
| chrX:17465616
|
C | CA | 10 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0164others(7): Show | 10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+89311dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17465616 | |||||
| chrX:17465616
|
C | CAA | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+89310_565+8931 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17465616 | |||||
| chrX:17465616
|
CA | C | 145 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0026others(142): Show | 145 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.565+89311delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17465616 | |||||
| chrX:17465616
|
CAA | C | 1 | a0002c0002t0001g0062 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.565+89310_565+8931 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17465616 | |||||
| chrX:17466117
|
A | G | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+89795A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17466117 | ||||||
| chrX:17466134
|
C | T | 1 | a0001c0003t0002g0142 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.565+89812C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17466134 | ||||||
| chrX:17466516
|
C | T | 2 | a0001c0003t0002g0128a0005c0006t0001g0162 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.565+90194C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17466516 | ||||||
| chrX:17466623
|
G | A | 1 | a0002c0002t0001g0010 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.565+90301G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17466623 | ||||||
| chrX:17466759
|
A | G | 45 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0041others(42): Show | 45 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.565+90437A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17466759 | ||||||
| chrX:17466854
|
A | G | 1 | a0001c0003t0002g0142 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.565+90532A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17466854 | ||||||
| chrX:17466857
|
C | G | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+90535C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17466857 | ||||||
| chrX:17466864
|
C | A | 1 | a0003c0004t0001g0055 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.565+90542C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17466864 | ||||||
| chrX:17466864
|
C | T | 163 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(160): Show | 163 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.565+90542C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17466864 | ||||||
| chrX:17467085
|
G | A | 40 | a0001c0001t0001g0029a0001c0001t0001g0048a0001c0001t0001g0049others(37): Show | 40 | HG00609.hp1 HG01358.hp1 HG02015.hp1 others(37): Show |
intron_variant | MODIFIER | c.565+90763G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17467085 | ||||||
| chrX:17467319
|
G | T | 1 | a0002c0002t0001g0025 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.565+90997G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17467319 | ||||||
| chrX:17467651
|
G | A | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+91329G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17467651 | ||||||
| chrX:17468044
|
CTGCT | C | 3 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110 | 3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+91724_565+9172 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17468044 | |||||
| chrX:17468435
|
C | CT | 18 | a0001c0001t0001g0029a0001c0001t0001g0048a0001c0001t0001g0049others(15): Show | 18 | HG00609.hp1 HG02056.hp1 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.565+92126dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17468435 | |||||
| chrX:17468447
|
T | A | 1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.565+92125T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17468447 | ||||||
| chrX:17468544
|
G | T | 1 | a0002c0002t0001g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.565+92222G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17468544 | ||||||
| chrX:17468723
|
A | T | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.565+92401A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17468723 | ||||||
| chrX:17468877
|
G | A | 2 | a0001c0001t0001g0052a0002c0002t0001g0051 | 2 | NA18612.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.565+92555G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17468877 | ||||||
| chrX:17468934
|
A | G | 2 | a0001c0003t0002g0142a0001c0003t0002g0155 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.565+92612A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17468934 | ||||||
| chrX:17468947
|
A | C | 1 | a0002c0002t0001g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.565+92625A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17468947 | ||||||
| chrX:17469071
|
C | T | 1 | a0006c0007t0002g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.565+92749C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17469071 | ||||||
| chrX:17469397
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.565+93075C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17469397 | ||||||
| chrX:17470269
|
A | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+93947A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17470269 | ||||||
| chrX:17470789
|
C | G | 1 | a0007c0009t0002g0160 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.565+94467C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17470789 | ||||||
| chrX:17470892
|
G | A | 20 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(17): Show | 20 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.565+94570G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17470892 | ||||||
| chrX:17470964
|
G | A | 1 | a0003c0004t0001g0013 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.565+94642G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17470964 | ||||||
| chrX:17471000
|
A | T | 23 | a0001c0001t0002g0099a0001c0001t0002g0116a0001c0001t0002g0120others(20): Show | 23 | HG01106.hp1 HG01243.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.565+94678A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17471000 | ||||||
| chrX:17471428
|
C | A | 4 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0144others(1): Show | 4 | NA18994.hp1 NA18995.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+95106C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17471428 | ||||||
| chrX:17472311
|
A | AAG | 5 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+96005_565+9600 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17472311 | |||||
| chrX:17472349
|
G | A | 1 | a0002c0002t0001g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.565+96027G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17472349 | ||||||
| chrX:17472353
|
G | A | 1 | a0002c0002t0001g0082 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.565+96031G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17472353 | ||||||
| chrX:17472563
|
A | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+96241A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17472563 | ||||||
| chrX:17472626
|
T | TA | 1 | a0002c0002t0001g0076 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.565+96306dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17472626 | |||||
| chrX:17472833
|
G | A | 1 | a0001c0001t0005g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.565+96511G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17472833 | ||||||
| chrX:17473322
|
A | C | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.565+97000A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17473322 | ||||||
| chrX:17473483
|
C | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+97161C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17473483 | ||||||
| chrX:17473698
|
C | A | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.565+97376C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17473698 | ||||||
| chrX:17473902
|
A | ATATT | 3 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110 | 3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+97602_565+9760 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17473902 | |||||
| chrX:17474041
|
C | T | 1 | a0004c0005t0010g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.565+97719C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474041 | ||||||
| chrX:17474045
|
A | G | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+97723A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474045 | ||||||
| chrX:17474097
|
G | A | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+97775G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474097 | ||||||
| chrX:17474100
|
T | C | 3 | a0001c0001t0002g0099a0001c0001t0002g0146a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+97778T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474100 | ||||||
| chrX:17474141
|
C | T | 12 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(9): Show | 12 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.565+97819C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474141 | ||||||
| chrX:17474158
|
A | G | 2 | a0001c0001t0002g0099a0009c0011t0002g0147 | 2 | HG01243.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.565+97836A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474158 | ||||||
| chrX:17474627
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.565+98305G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474627 | ||||||
| chrX:17474850
|
T | C | 7 | a0001c0001t0005g0111a0001c0003t0002g0101a0006c0007t0002g0115others(4): Show | 7 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.565+98528T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474850 | ||||||
| chrX:17474852
|
T | G | 7 | a0001c0001t0005g0111a0001c0003t0002g0101a0006c0007t0002g0115others(4): Show | 7 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.565+98530T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474852 | ||||||
| chrX:17474915
|
A | G | 8 | a0001c0001t0002g0099a0001c0001t0005g0111a0001c0003t0002g0101others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.565+98593A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474915 | ||||||
| chrX:17475013
|
TG | T | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+98693delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17475013 | |||||
| chrX:17475118
|
C | CT | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+98798dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17475118 | |||||
| chrX:17475242
|
TG | T | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+98922delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17475242 | |||||
| chrX:17475258
|
A | AC | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+98937dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17475258 | |||||
| chrX:17475535
|
C | A | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+99213C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17475535 | ||||||
| chrX:17475649
|
A | G | 12 | a0001c0001t0002g0099a0001c0001t0002g0146a0001c0001t0002g0164others(9): Show | 12 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.565+99327A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17475649 | ||||||
| chrX:17475831
|
C | G | 10 | a0001c0001t0002g0099a0001c0001t0005g0111a0001c0003t0002g0101others(7): Show | 10 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+99509C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17475831 | ||||||
| chrX:17475835
|
G | A | 2 | a0002c0002t0001g0138a0002c0002t0001g0139 | 2 | HG00673.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.565+99513G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17475835 | ||||||
| chrX:17476013
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+99691G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17476013 | ||||||
| chrX:17476020
|
GA | G | 4 | a0001c0001t0001g0026a0002c0002t0001g0015a0002c0002t0001g0053others(1): Show | 4 | HG02083.hp1 NA18747.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+99700delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17476020 | |||||
| chrX:17476024
|
GC | G | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+99704delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17476024 | |||||
| chrX:17476176
|
A | G | 5 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+99854A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17476176 | ||||||
| chrX:17476347
|
G | A | 2 | a0001c0001t0002g0099a0009c0011t0002g0147 | 2 | HG01243.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.565+100025G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17476347 | ||||||
| chrX:17476478
|
T | C | 41 | a0001c0001t0001g0029a0001c0001t0001g0048a0001c0001t0001g0049others(38): Show | 41 | HG00609.hp1 HG00639.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.565+100156T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17476478 | ||||||
| chrX:17476489
|
T | C | 2 | a0001c0003t0002g0142a0001c0003t0002g0155 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.565+100167T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17476489 | ||||||
| chrX:17476599
|
T | G | 1 | a0002c0002t0001g0015 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.565+100277T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17476599 | ||||||
| chrX:17476850
|
A | T | 5 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+100528A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17476850 | ||||||
| chrX:17476941
|
T | TG | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+100620dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17476941 | |||||
| chrX:17477291
|
T | C | 5 | a0002c0002t0001g0003a0002c0002t0001g0034a0002c0002t0001g0040others(2): Show | 5 | HG01167.hp1 HG02735.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+100969T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17477291 | ||||||
| chrX:17477305
|
C | T | 1 | a0002c0002t0001g0003 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.565+100983C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17477305 | ||||||
| chrX:17477384
|
C | T | 1 | a0004c0005t0003g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.565+101062C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17477384 | ||||||
| chrX:17477434
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.565+101112C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17477434 | ||||||
| chrX:17477442
|
T | TC | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+101123dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17477442 | |||||
| chrX:17477471
|
T | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+101149T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17477471 | ||||||
| chrX:17477479
|
C | CT | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+101161dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17477479 | |||||
| chrX:17478019
|
G | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+101697G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17478019 | ||||||
| chrX:17478077
|
G | A | 16 | a0001c0001t0002g0099a0001c0001t0002g0116a0001c0001t0002g0120others(13): Show | 16 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.565+101755G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17478077 | ||||||
| chrX:17478209
|
C | T | 108 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.565+101887C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17478209 | ||||||
| chrX:17478597
|
G | GTCT | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+102275_565+102 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17478597 | ||||||
| chrX:17478598
|
A | C | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+102276A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17478598 | ||||||
| chrX:17478916
|
T | A | 143 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(140): Show | 143 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.565+102594T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17478916 | ||||||
| chrX:17479677
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0015g0079 | 2 | NA18952.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.565+103355G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17479677 | ||||||
| chrX:17479816
|
C | CA | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+103499dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17479816 | |||||
| chrX:17479979
|
C | G | 108 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.565+103657C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17479979 | ||||||
| chrX:17481320
|
G | A | 37 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0061others(34): Show | 37 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.565+104998G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17481320 | ||||||
| chrX:17481384
|
G | GT | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+105065dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17481384 | |||||
| chrX:17481430
|
A | AT | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+105116dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17481430 | |||||
| chrX:17481570
|
G | GT | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+105253dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17481570 | |||||
| chrX:17481610
|
GA | G | 37 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0061others(34): Show | 37 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.565+105294delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17481610 | |||||
| chrX:17481847
|
CT | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+105527delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17481847 | |||||
| chrX:17481969
|
CTG | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+105653_565+105 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17481969 | |||||
| chrX:17482011
|
C | T | 2 | a0002c0002t0001g0148a0002c0002t0001g0152 | 2 | HG00642.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.565+105689C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17482011 | ||||||
| chrX:17482094
|
A | G | 3 | a0001c0001t0017g0154a0002c0002t0011g0020a0004c0005t0010g0097 | 3 | HG01975.hp1 HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.565+105772A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17482094 | ||||||
| chrX:17482104
|
T | TG | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+105786dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17482104 | |||||
| chrX:17482275
|
A | C | 1 | a0004c0005t0003g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.565+105953A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17482275 | ||||||
| chrX:17482539
|
A | G | 1 | a0002c0002t0001g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.565+106217A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17482539 | ||||||
| chrX:17482605
|
T | C | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+106283T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17482605 | ||||||
| chrX:17482659
|
A | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+106337A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17482659 | ||||||
| chrX:17482913
|
G | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+106591G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17482913 | ||||||
| chrX:17482919
|
G | A | 5 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+106597G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17482919 | ||||||
| chrX:17482978
|
C | T | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+106656C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17482978 | ||||||
| chrX:17483007
|
G | C | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+106685G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17483007 | ||||||
| chrX:17483041
|
G | GC | 110 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(107): Show | 110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+106723dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17483041 | |||||
| chrX:17483091
|
AT | A | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+106774delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17483091 | |||||
| chrX:17483125
|
GT | G | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+106806delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17483125 | |||||
| chrX:17483253
|
TA | T | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+106937delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17483253 | |||||
| chrX:17483550
|
A | C | 2 | a0003c0004t0001g0149a0010c0012t0001g0150 | 2 | NA18948.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.565+107228A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17483550 | ||||||
| chrX:17483664
|
T | TG | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+107344dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17483664 | |||||
| chrX:17483971
|
TG | T | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+107652delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17483971 | |||||
| chrX:17484472
|
A | G | 1 | a0004c0005t0010g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.565+108150A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17484472 | ||||||
| chrX:17484630
|
GGGCTCTG others(62): Show |
G | 110 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(107): Show | 110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+108312_565+108 others(75): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17484630 | |||||
| chrX:17484890
|
A | G | 1 | a0002c0002t0001g0007 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.565+108568A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17484890 | ||||||
| chrX:17484952
|
T | G | 3 | a0002c0002t0001g0018a0002c0002t0001g0028a0002c0002t0001g0123 | 3 | HG00639.hp1 HG01074.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.565+108630T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17484952 | ||||||
| chrX:17484959
|
A | C | 109 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(106): Show | 109 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.565+108637A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17484959 | ||||||
| chrX:17484966
|
G | C | 3 | a0002c0002t0001g0018a0002c0002t0001g0028a0002c0002t0001g0123 | 3 | HG00639.hp1 HG01074.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.565+108644G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17484966 | ||||||
| chrX:17485193
|
T | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+108871T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17485193 | ||||||
| chrX:17485216
|
AG | A | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+108898delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17485216 | |||||
| chrX:17485251
|
G | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+108929G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17485251 | ||||||
| chrX:17485768
|
G | C | 111 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(108): Show | 111 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.565+109446G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17485768 | ||||||
| chrX:17486061
|
C | T | 111 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(108): Show | 111 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.565+109739C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17486061 | ||||||
| chrX:17486239
|
T | C | 110 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(107): Show | 110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+109917T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17486239 | ||||||
| chrX:17486452
|
A | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+110130A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17486452 | ||||||
| chrX:17486712
|
A | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+110390A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17486712 | ||||||
| chrX:17486794
|
T | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+110472T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17486794 | ||||||
| chrX:17486937
|
G | A | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+110615G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17486937 | ||||||
| chrX:17487129
|
T | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+110807T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17487129 | ||||||
| chrX:17487289
|
G | C | 4 | a0001c0001t0002g0143a0001c0003t0002g0128a0005c0006t0001g0162others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+110967G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17487289 | ||||||
| chrX:17487363
|
G | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+111041G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17487363 | ||||||
| chrX:17487890
|
G | C | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.565+111568G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17487890 | ||||||
| chrX:17488305
|
A | C | 110 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(107): Show | 110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+111983A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17488305 | ||||||
| chrX:17488495
|
C | T | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+112173C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17488495 | ||||||
| chrX:17488573
|
C | T | 8 | a0001c0001t0005g0111a0001c0003t0002g0101a0006c0007t0002g0115others(5): Show | 8 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.565+112251C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17488573 | ||||||
| chrX:17488658
|
T | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+112336T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17488658 | ||||||
| chrX:17488904
|
C | CTACATTA others(2893): Show |
1 | a0002c0002t0001g0152 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.565+112598_565+112 others(2906): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17488904 | |||||
| chrX:17488904
|
C | CTACATTA others(2894): Show |
1 | a0002c0002t0001g0148 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.565+112598_565+112 others(2907): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17488904 | |||||
| chrX:17489079
|
A | G | 1 | a0013c0016t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.565+112757A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489079 | ||||||
| chrX:17489143
|
A | G | 1 | a0004c0005t0003g0117 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.565+112821A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489143 | ||||||
| chrX:17489289
|
T | TC | 1 | a0002c0002t0001g0011 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.565+112969dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17489289 | |||||
| chrX:17489332
|
A | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+113010A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489332 | ||||||
| chrX:17489383
|
G | GT | 1 | a0002c0002t0001g0011 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.565+113063dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17489383 | |||||
| chrX:17489420
|
T | C | 110 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(107): Show | 110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+113098T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489420 | ||||||
| chrX:17489463
|
G | A | 110 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(107): Show | 110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+113141G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489463 | ||||||
| chrX:17489478
|
T | TTTG | 1 | a0001c0001t0009g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.565+113180_565+113 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17489478 | |||||
| chrX:17489502
|
G | T | 110 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(107): Show | 110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+113180G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489502 | ||||||
| chrX:17489526
|
C | CG | 1 | a0002c0002t0001g0011 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.565+113204_565+113 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489526 | ||||||
| chrX:17489527
|
A | C | 1 | a0002c0002t0001g0011 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.565+113205A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489527 | ||||||
| chrX:17489527
|
A | G | 105 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(102): Show | 105 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.565+113205A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489527 | ||||||
| chrX:17489582
|
G | A | 2 | a0006c0007t0002g0115a0006c0007t0002g0118 | 2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.565+113260G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489582 | ||||||
| chrX:17489620
|
T | TG | 1 | a0002c0002t0001g0011 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.565+113301dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17489620 | |||||
| chrX:17489645
|
GC | G | 1 | a0002c0002t0001g0011 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.565+113326delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17489645 | |||||
| chrX:17489705
|
T | TC | 1 | a0002c0002t0001g0011 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.565+113384dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17489705 | |||||
| chrX:17489739
|
G | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0005g0103 | 3 | HG03139.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.565+113417G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489739 | ||||||
| chrX:17489793
|
T | C | 1 | a0002c0002t0001g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.565+113471T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489793 | ||||||
| chrX:17489801
|
C | T | 109 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(106): Show | 109 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.565+113479C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489801 | ||||||
| chrX:17489817
|
A | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+113495A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489817 | ||||||
| chrX:17489913
|
G | T | 1 | a0002c0002t0016g0005 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.565+113591G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489913 | ||||||
| chrX:17490235
|
T | G | 3 | a0002c0002t0001g0014a0002c0002t0001g0023a0002c0002t0001g0030 | 3 | HG00408.hp2 HG01975.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.565+113913T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17490235 | ||||||
| chrX:17490246
|
T | G | 110 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(107): Show | 110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+113924T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17490246 | ||||||
| chrX:17490256
|
A | C | 3 | a0002c0002t0001g0014a0002c0002t0001g0023a0002c0002t0001g0030 | 3 | HG00408.hp2 HG01975.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.565+113934A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17490256 | ||||||
| chrX:17490505
|
G | T | 1 | a0001c0003t0002g0142 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.565+114183G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17490505 | ||||||
| chrX:17490536
|
T | G | 1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.565+114214T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17490536 | ||||||
| chrX:17490839
|
A | G | 8 | a0001c0001t0005g0111a0001c0003t0002g0101a0006c0007t0002g0115others(5): Show | 8 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.565+114517A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17490839 | ||||||
| chrX:17491081
|
T | C | 5 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+114759T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491081 | ||||||
| chrX:17491205
|
C | G | 114 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(111): Show | 114 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.565+114883C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491205 | ||||||
| chrX:17491277
|
C | T | 3 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110 | 3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+114955C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491277 | ||||||
| chrX:17491397
|
G | T | 3 | a0002c0002t0001g0014a0002c0002t0001g0023a0002c0002t0001g0030 | 3 | HG00408.hp2 HG01975.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.565+115075G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491397 | ||||||
| chrX:17491434
|
G | A | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+115112G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491434 | ||||||
| chrX:17491701
|
G | A | 1 | a0002c0002t0001g0011 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.565+115379G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491701 | ||||||
| chrX:17491723
|
G | A | 8 | a0001c0001t0005g0111a0001c0003t0002g0101a0006c0007t0002g0115others(5): Show | 8 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.565+115401G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491723 | ||||||
| chrX:17491754
|
C | CT | 10 | a0001c0001t0001g0029a0001c0001t0002g0116a0001c0001t0002g0120others(7): Show | 10 | HG01928.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+115450dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17491754 | |||||
| chrX:17491754
|
C | CTT | 1 | a0004c0005t0003g0117 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.565+115449_565+115 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17491754 | |||||
| chrX:17491754
|
CT | C | 3 | a0001c0001t0001g0151a0002c0002t0001g0028a0002c0002t0001g0080 | 3 | HG00408.hp1 HG01256.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.565+115450delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17491754 | |||||
| chrX:17491836
|
G | A | 1 | a0002c0002t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.565+115514G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491836 | ||||||
| chrX:17491861
|
A | T | 1 | a0002c0002t0014g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.565+115539A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491861 | ||||||
| chrX:17491940
|
T | C | 109 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(106): Show | 109 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.565+115618T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491940 | ||||||
| chrX:17492247
|
T | C | 3 | a0001c0001t0002g0121a0001c0001t0006g0112a0004c0005t0003g0117 | 3 | HG02280.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.565+115925T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17492247 | ||||||
| chrX:17492260
|
T | C | 5 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+115938T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17492260 | ||||||
| chrX:17492455
|
T | C | 5 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+116133T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17492455 | ||||||
| chrX:17492705
|
C | T | 2 | a0001c0001t0002g0143a0007c0009t0002g0160 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.565+116383C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17492705 | ||||||
| chrX:17492748
|
A | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+116426A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17492748 | ||||||
| chrX:17492765
|
G | A | 41 | a0001c0001t0001g0029a0001c0001t0001g0048a0001c0001t0001g0049others(38): Show | 41 | HG00609.hp1 HG00639.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.565+116443G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17492765 | ||||||
| chrX:17493329
|
T | G | 1 | a0006c0007t0002g0118 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565+117007T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17493329 | ||||||
| chrX:17493427
|
T | G | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.565+117105T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17493427 | ||||||
| chrX:17493612
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0007g0073a0001c0001t0007g0102 | 3 | NA18955.hp1 NA18962.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.565+117290G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17493612 | ||||||
| chrX:17493730
|
G | T | 109 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(106): Show | 109 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.565+117408G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17493730 | ||||||
| chrX:17493734
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.565+117412G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17493734 | ||||||
| chrX:17493924
|
T | G | 111 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(108): Show | 111 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.565+117602T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17493924 | ||||||
| chrX:17494076
|
C | CT | 53 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0056others(50): Show | 53 | HG00639.hp1 HG01074.hp1 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.565+117776dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17494076 | |||||
| chrX:17494076
|
C | CTT | 40 | a0001c0001t0001g0029a0001c0001t0001g0048a0001c0001t0001g0049others(37): Show | 40 | HG00609.hp1 HG00639.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.565+117775_565+117 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17494076 | |||||
| chrX:17494076
|
C | CTTT | 2 | a0001c0001t0015g0079a0002c0002t0001g0062 | 2 | NA18952.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.565+117774_565+117 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17494076 | |||||
| chrX:17494076
|
CT | C | 2 | a0001c0001t0001g0041a0001c0003t0002g0019 | 2 | HG01258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.565+117776delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17494076 | |||||
| chrX:17494286
|
C | G | 110 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(107): Show | 110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+117964C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17494286 | ||||||
| chrX:17494579
|
C | T | 1 | a0008c0010t0003g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.565+118257C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17494579 | ||||||
| chrX:17495151
|
C | T | 1 | a0004c0005t0010g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.565+118829C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17495151 | ||||||
| chrX:17495956
|
G | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0005g0103 | 3 | HG03139.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.565+119634G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17495956 | ||||||
| chrX:17496094
|
C | G | 1 | a0005c0006t0008g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565+119772C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17496094 | ||||||
| chrX:17496477
|
C | A | 3 | a0001c0001t0001g0104a0001c0001t0007g0073a0001c0001t0007g0102 | 3 | NA18955.hp1 NA18962.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.565+120155C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17496477 | ||||||
| chrX:17496640
|
A | C | 4 | a0001c0001t0002g0143a0001c0003t0002g0128a0005c0006t0001g0162others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+120318A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17496640 | ||||||
| chrX:17496695
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0005g0103 | 3 | HG03139.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.565+120373C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17496695 | ||||||
| chrX:17497077
|
C | T | 1 | a0002c0002t0001g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.565+120755C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17497077 | ||||||
| chrX:17497377
|
C | T | 1 | a0002c0002t0001g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.565+121055C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17497377 | ||||||
| chrX:17497819
|
A | G | 106 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(103): Show | 106 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.565+121497A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17497819 | ||||||
| chrX:17498171
|
T | A | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+121849T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17498171 | ||||||
| chrX:17498232
|
G | A | 1 | a0006c0007t0002g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.565+121910G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17498232 | ||||||
| chrX:17498411
|
T | C | 1 | a0004c0005t0010g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.565+122089T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17498411 | ||||||
| chrX:17498748
|
A | T | 113 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(110): Show | 113 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.565+122426A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17498748 | ||||||
| chrX:17499044
|
T | C | 6 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+122722T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17499044 | ||||||
| chrX:17499602
|
C | CA | 5 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+123280_565+123 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17499602 | ||||||
| chrX:17500037
|
G | A | 6 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(3): Show | 6 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+123715G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17500037 | ||||||
| chrX:17500115
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.565+123793G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17500115 | ||||||
| chrX:17500191
|
G | A | 1 | a0002c0002t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.565+123869G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17500191 | ||||||
| chrX:17500457
|
T | C | 6 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(3): Show | 6 | HG02280.hp1 HG02717.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+124135T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17500457 | ||||||
| chrX:17500668
|
T | C | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+124346T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17500668 | ||||||
| chrX:17500825
|
C | T | 5 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+124503C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17500825 | ||||||
| chrX:17500956
|
A | ATTG | 117 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(114): Show | 117 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.565+124636_565+124 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17500956 | |||||
| chrX:17501134
|
T | A | 1 | a0002c0002t0001g0007 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.565+124812T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17501134 | ||||||
| chrX:17501197
|
C | T | 2 | a0001c0003t0002g0128a0005c0006t0001g0162 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.565+124875C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17501197 | ||||||
| chrX:17501355
|
G | GA | 54 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0036others(51): Show | 54 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.565+125044dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17501355 | |||||
| chrX:17501355
|
G | GAA | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+125043_565+125 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17501355 | |||||
| chrX:17502493
|
TAAGAAGT others(308): Show |
T | 112 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(109): Show | 112 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.565+126186_565+126 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17502493 | |||||
| chrX:17502788
|
C | CA | 4 | a0001c0001t0001g0041a0001c0001t0001g0134a0001c0001t0001g0144others(1): Show | 4 | HG00642.hp1 HG02451.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+126488dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17502788 | |||||
| chrX:17502788
|
CA | C | 1 | a0002c0002t0001g0091 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.565+126488delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17502788 | |||||
| chrX:17503306
|
T | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+126984T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17503306 | ||||||
| chrX:17503379
|
T | G | 8 | a0001c0001t0005g0111a0001c0003t0002g0101a0006c0007t0002g0115others(5): Show | 8 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.565+127057T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17503379 | ||||||
| chrX:17503691
|
A | G | 5 | a0001c0001t0001g0127a0001c0001t0009g0125a0004c0005t0003g0136others(2): Show | 5 | HG01071.hp2 HG02647.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+127369A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17503691 | ||||||
| chrX:17503911
|
C | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+127589C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17503911 | ||||||
| chrX:17504360
|
T | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+128038T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17504360 | ||||||
| chrX:17505627
|
G | GT | 13 | a0001c0001t0001g0012a0001c0001t0005g0111a0001c0001t0017g0154others(10): Show | 13 | HG00642.hp1 HG01975.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.565+129319dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17505627 | |||||
| chrX:17505627
|
G | GTT | 2 | a0001c0001t0002g0164a0006c0008t0008g0113 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.565+129318_565+129 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17505627 | |||||
| chrX:17505627
|
GT | G | 1 | a0002c0002t0001g0074 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.565+129319delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17505627 | |||||
| chrX:17505875
|
A | G | 151 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(148): Show | 151 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.565+129553A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17505875 | ||||||
| chrX:17506423
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+130101A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17506423 | ||||||
| chrX:17506461
|
G | A | 27 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0061others(24): Show | 27 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.565+130139G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17506461 | ||||||
| chrX:17506527
|
T | TAATA | 9 | a0001c0001t0002g0004a0001c0001t0002g0093a0001c0001t0002g0096others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.565+130243_565+130 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17506527 | |||||
| chrX:17506527
|
T | TAATAAAT others(1): Show |
1 | a0001c0001t0001g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.565+130239_565+130 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17506527 | |||||
| chrX:17506527
|
TAATA | T | 15 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0124others(12): Show | 15 | HG00408.hp1 HG00408.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.565+130243_565+130 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17506527 | |||||
| chrX:17506527
|
TAATAAAT others(1): Show |
T | 6 | a0001c0001t0001g0068a0001c0001t0002g0106a0001c0001t0002g0107others(3): Show | 6 | HG01106.hp1 HG02258.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+130239_565+130 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17506527 | |||||
| chrX:17506527
|
TAATAAAT others(5): Show |
T | 1 | a0002c0002t0001g0077 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.565+130235_565+130 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17506527 | |||||
| chrX:17506561
|
A | ATAAG | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.565+130242_565+130 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17506561 | |||||
| chrX:17506565
|
A | ATAAATAA others(1): Show |
3 | a0001c0001t0001g0104a0001c0001t0009g0122a0008c0010t0003g0158 | 3 | HG02615.hp2 HG02723.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.565+130246_565+130 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17506565 | |||||
| chrX:17506565
|
A | ATAAG | 22 | a0001c0001t0001g0048a0001c0001t0002g0099a0001c0001t0005g0103others(19): Show | 22 | HG00639.hp1 HG01074.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.565+130247_565+130 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17506565 | |||||
| chrX:17506565
|
A | G | 85 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(82): Show | 85 | HG00280.hp1 HG00609.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.565+130243A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17506565 | ||||||
| chrX:17507106
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+130784A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17507106 | ||||||
| chrX:17507109
|
C | T | 2 | a0006c0008t0001g0114a0006c0008t0008g0113 | 2 | HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.565+130787C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17507109 | ||||||
| chrX:17507294
|
T | C | 1 | a0002c0002t0001g0010 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.565+130972T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17507294 | ||||||
| chrX:17507376
|
C | T | 1 | a0002c0002t0001g0076 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.565+131054C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17507376 | ||||||
| chrX:17507672
|
G | A | 1 | a0002c0002t0001g0071 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.565+131350G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17507672 | ||||||
| chrX:17507728
|
G | C | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+131406G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17507728 | ||||||
| chrX:17507751
|
A | G | 116 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(113): Show | 116 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.565+131429A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17507751 | ||||||
| chrX:17508116
|
AATGGTAC others(17): Show |
A | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+131808_565+131 others(30): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17508116 | |||||
| chrX:17508242
|
C | T | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+131920C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17508242 | ||||||
| chrX:17508257
|
A | G | 114 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(111): Show | 114 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.565+131935A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17508257 | ||||||
| chrX:17508270
|
C | T | 1 | a0002c0002t0001g0023 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.565+131948C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17508270 | ||||||
| chrX:17508292
|
G | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+131970G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17508292 | ||||||
| chrX:17508371
|
T | G | 5 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+132049T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17508371 | ||||||
| chrX:17508470
|
GTTGT | G | 8 | a0001c0001t0001g0137a0001c0001t0002g0043a0001c0001t0012g0044others(5): Show | 8 | HG01109.hp1 HG01167.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.565+132163_565+132 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17508470 | |||||
| chrX:17508655
|
A | G | 1 | a0004c0005t0003g0117 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.565+132333A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17508655 | ||||||
| chrX:17508841
|
G | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+132519G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17508841 | ||||||
| chrX:17509027
|
T | TG | 2 | a0006c0008t0001g0114a0006c0008t0008g0113 | 2 | HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.565+132707dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17509027 | |||||
| chrX:17509201
|
C | G | 112 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(109): Show | 112 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.565+132879C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17509201 | ||||||
| chrX:17509206
|
A | AATTT | 20 | a0001c0001t0001g0029a0001c0001t0002g0002a0001c0001t0002g0093others(17): Show | 20 | HG01069.hp1 HG01071.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.565+132919_565+132 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17509206 | |||||
| chrX:17509206
|
A | AATTTATT others(1): Show |
5 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0001t0002g0004others(2): Show | 5 | HG02451.hp1 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+132915_565+132 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17509206 | |||||
| chrX:17509206
|
AATTT | A | 82 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0048others(79): Show | 82 | HG00280.hp1 HG00609.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.565+132919_565+132 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17509206 | |||||
| chrX:17509678
|
GA | G | 3 | a0001c0001t0002g0099a0001c0001t0009g0122a0009c0011t0002g0147 | 3 | HG01243.hp1 HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.565+133357delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17509678 | ||||||
| chrX:17509698
|
C | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+133376C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17509698 | ||||||
| chrX:17509750
|
A | G | 2 | a0001c0003t0002g0142a0001c0003t0002g0155 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.565+133428A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17509750 | ||||||
| chrX:17509779
|
A | C | 115 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(112): Show | 115 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.565+133457A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17509779 | ||||||
| chrX:17509936
|
G | T | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+133614G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17509936 | ||||||
| chrX:17509982
|
AT | A | 1 | a0002c0002t0001g0105 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.565+133666delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17509982 | |||||
| chrX:17510481
|
G | C | 1 | a0001c0001t0002g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.565+134159G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17510481 | ||||||
| chrX:17510493
|
G | A | 110 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(107): Show | 110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+134171G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17510493 | ||||||
| chrX:17510721
|
A | C | 5 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+134399A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17510721 | ||||||
| chrX:17511078
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.565+134756A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17511078 | ||||||
| chrX:17511209
|
A | G | 116 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(113): Show | 116 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.565+134887A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17511209 | ||||||
| chrX:17511860
|
CCTT | C | 48 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0036others(45): Show | 48 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.565+135542_565+135 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17511860 | |||||
| chrX:17512201
|
C | T | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+135879C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17512201 | ||||||
| chrX:17512457
|
G | C | 17 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0134others(14): Show | 17 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.565+136135G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17512457 | ||||||
| chrX:17512638
|
A | C | 54 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0036others(51): Show | 54 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.565+136316A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17512638 | ||||||
| chrX:17512792
|
C | T | 1 | a0001c0001t0002g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.565+136470C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17512792 | ||||||
| chrX:17512794
|
T | TA | 59 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0036others(56): Show | 59 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.565+136473dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17512794 | |||||
| chrX:17513041
|
G | GT | 1 | a0002c0002t0001g0105 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.565+136723dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17513041 | |||||
| chrX:17514158
|
C | A | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+137836C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17514158 | ||||||
| chrX:17514165
|
G | T | 13 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0124others(10): Show | 13 | HG00408.hp2 HG01258.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.565+137843G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17514165 | ||||||
| chrX:17514325
|
A | C | 1 | a0002c0015t0001g0046 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.565+138003A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17514325 | ||||||
| chrX:17515061
|
T | A | 6 | a0001c0001t0005g0111a0001c0003t0002g0101a0006c0007t0002g0115others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+138739T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17515061 | ||||||
| chrX:17515370
|
AG | A | 16 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(13): Show | 16 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.565+139050delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17515370 | |||||
| chrX:17516044
|
T | TA | 18 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(15): Show | 18 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.565+139737dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516044 | |||||
| chrX:17516044
|
T | TAA | 1 | a0001c0001t0006g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.565+139736_565+139 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516044 | |||||
| chrX:17516044
|
TA | T | 1 | a0001c0001t0001g0134 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.565+139737delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516044 | |||||
| chrX:17516246
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.565+139924C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516246 | ||||||
| chrX:17516267
|
G | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+139945G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516267 | ||||||
| chrX:17516314
|
C | G | 2 | a0002c0002t0011g0020a0004c0005t0010g0097 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.565+139992C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516314 | ||||||
| chrX:17516417
|
T | C | 16 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(13): Show | 16 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.565+140095T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516417 | ||||||
| chrX:17516565
|
ACACGCG | A | 3 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110 | 3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+140247_565+140 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516565 | |||||
| chrX:17516567
|
ACG | A | 6 | a0001c0001t0001g0070a0001c0001t0001g0127a0001c0001t0009g0125others(3): Show | 6 | HG01071.hp2 HG02647.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+140249_565+140 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516567 | |||||
| chrX:17516569
|
G | A | 15 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0121others(12): Show | 15 | HG02145.hp1 HG02280.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.565+140247G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516569 | ||||||
| chrX:17516569
|
GCGCA | G | 5 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0004g0069others(2): Show | 5 | HG02132.hp1 NA18989.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+140249_565+140 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516569 | |||||
| chrX:17516571
|
G | GCA | 37 | a0001c0001t0001g0026a0001c0001t0001g0048a0001c0001t0001g0049others(34): Show | 37 | HG00621.hp1 HG00639.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.565+140283_565+140 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516571 | |||||
| chrX:17516571
|
G | GCACA | 4 | a0001c0001t0001g0050a0002c0002t0001g0054a0002c0002t0001g0108others(1): Show | 4 | HG02056.hp1 NA18974.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+140281_565+140 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516571 | |||||
| chrX:17516571
|
G | GCACACA | 1 | a0001c0001t0001g0057 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.565+140279_565+140 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516571 | |||||
| chrX:17516571
|
G | GCACACAC others(1): Show |
1 | a0002c0002t0001g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.565+140277_565+140 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516571 | |||||
| chrX:17516571
|
GCA | G | 31 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0061others(28): Show | 31 | HG00140.hp1 HG00673.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.565+140283_565+140 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516571 | |||||
| chrX:17516571
|
GCACA | G | 8 | a0001c0001t0001g0052a0001c0001t0002g0002a0001c0001t0002g0164others(5): Show | 8 | HG02055.hp1 HG02293.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.565+140281_565+140 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516571 | |||||
| chrX:17516571
|
GCACACAC others(5): Show |
G | 1 | a0002c0002t0001g0021 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.565+140273_565+140 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516571 | |||||
| chrX:17516573
|
A | G | 2 | a0001c0003t0002g0142a0001c0003t0002g0155 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.565+140251A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516573 | ||||||
| chrX:17516577
|
A | G | 3 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110 | 3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+140255A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516577 | ||||||
| chrX:17516773
|
G | GCA | 1 | a0001c0001t0005g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.565+140469_565+140 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516773 | |||||
| chrX:17516773
|
GCACACA | G | 3 | a0001c0001t0001g0022a0001c0001t0004g0163a0002c0002t0001g0001 | 3 | HG01261.hp1 HG02135.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.565+140465_565+140 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516773 | |||||
| chrX:17516791
|
A | G | 1 | a0002c0002t0001g0023 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.565+140469A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516791 | ||||||
| chrX:17516863
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.565+140541C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516863 | ||||||
| chrX:17516898
|
T | C | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.565+140576T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516898 | ||||||
| chrX:17516987
|
C | A | 6 | a0001c0001t0001g0041a0001c0001t0002g0004a0001c0001t0002g0093others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+140665C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516987 | ||||||
| chrX:17517015
|
G | A | 1 | a0013c0016t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.565+140693G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17517015 | ||||||
| chrX:17517290
|
C | T | 16 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(13): Show | 16 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.565+140968C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17517290 | ||||||
| chrX:17517414
|
G | T | 2 | a0002c0002t0001g0138a0002c0002t0001g0139 | 2 | HG00673.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.565+141092G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17517414 | ||||||
| chrX:17517753
|
T | C | 1 | a0002c0002t0001g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.565+141431T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17517753 | ||||||
| chrX:17517794
|
T | A | 16 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(13): Show | 16 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.565+141472T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17517794 | ||||||
| chrX:17518084
|
C | G | 16 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(13): Show | 16 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.565+141762C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17518084 | ||||||
| chrX:17518219
|
C | T | 1 | a0005c0006t0008g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565+141897C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17518219 | ||||||
| chrX:17518346
|
A | G | 3 | a0002c0002t0001g0014a0002c0002t0001g0023a0002c0002t0001g0030 | 3 | HG00408.hp2 HG01975.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.565+142024A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17518346 | ||||||
| chrX:17519127
|
C | T | 1 | a0001c0001t0013g0059 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.565+142805C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17519127 | ||||||
| chrX:17519185
|
TA | T | 16 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(13): Show | 16 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.565+142867delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17519185 | |||||
| chrX:17519448
|
C | G | 3 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110 | 3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+143126C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17519448 | ||||||
| chrX:17519750
|
AC | A | 1 | a0002c0002t0001g0054 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.565+143431delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17519750 | |||||
| chrX:17519829
|
G | A | 2 | a0001c0001t0002g0164a0004c0005t0003g0100 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.565+143507G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17519829 | ||||||
| chrX:17519925
|
T | TA | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+143603_565+143 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17519925 | ||||||
| chrX:17520131
|
G | T | 5 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+143809G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17520131 | ||||||
| chrX:17520662
|
G | A | 18 | a0001c0001t0002g0085a0001c0001t0002g0106a0001c0001t0002g0107others(15): Show | 18 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.565+144340G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17520662 | ||||||
| chrX:17520720
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.565+144398G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17520720 | ||||||
| chrX:17521366
|
C | CT | 1 | a0004c0005t0010g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.565+145057dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | |||||
| chrX:17521366
|
C | CTTTTTT | 4 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0006g0112others(1): Show | 4 | HG03098.hp1 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+145052_565+145 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | |||||
| chrX:17521366
|
C | CTTTTTTT others(11): Show |
3 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110 | 3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+145057_565+145 others(24): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | |||||
| chrX:17521366
|
C | CTTTTTTT others(15): Show |
1 | a0004c0005t0003g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.565+145057_565+145 others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | |||||
| chrX:17521366
|
C | CTTTTTTT others(16): Show |
2 | a0001c0001t0002g0164a0001c0003t0002g0101 | 2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.565+145057_565+145 others(29): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | |||||
| chrX:17521366
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0005g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.565+145057_565+145 others(31): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | |||||
| chrX:17521366
|
C | CTTTTTTT others(24): Show |
1 | a0006c0007t0002g0118 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565+145057_565+145 others(37): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | |||||
| chrX:17521366
|
C | CTTTTTTT others(26): Show |
1 | a0006c0007t0002g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.565+145057_565+145 others(39): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | |||||
| chrX:17521366
|
C | CTTTTTTT others(27): Show |
1 | a0001c0001t0002g0085 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.565+145057_565+145 others(40): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | |||||
| chrX:17521366
|
C | CTTTTTTT others(28): Show |
1 | a0008c0010t0003g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.565+145057_565+145 others(41): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | |||||
| chrX:17521366
|
C | CTTTTTTT others(32): Show |
1 | a0006c0008t0001g0114 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.565+145057_565+145 others(45): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | |||||
| chrX:17521366
|
C | CTTTTTTT others(34): Show |
1 | a0006c0008t0008g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.565+145057_565+145 others(47): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | |||||
| chrX:17521366
|
C | CTTTTTTT others(40): Show |
1 | a0013c0016t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.565+145057_565+145 others(53): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | |||||
| chrX:17521433
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.565+145111G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17521433 | ||||||
| chrX:17521449
|
C | T | 9 | a0001c0001t0002g0085a0001c0001t0005g0111a0001c0003t0002g0101others(6): Show | 9 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+145127C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17521449 | ||||||
| chrX:17521472
|
C | T | 9 | a0001c0001t0002g0085a0001c0001t0005g0111a0001c0003t0002g0101others(6): Show | 9 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+145150C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17521472 | ||||||
| chrX:17521475
|
A | G | 4 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0006g0112others(1): Show | 4 | HG03098.hp1 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+145153A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17521475 | ||||||
| chrX:17522059
|
T | C | 1 | a0001c0001t0006g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.565+145737T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17522059 | ||||||
| chrX:17522318
|
G | A | 1 | a0002c0002t0001g0156 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.565+145996G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17522318 | ||||||
| chrX:17522493
|
G | GC | 38 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0134others(35): Show | 38 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(35): Show |
intron_variant | MODIFIER | c.565+146184dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522493 | |||||
| chrX:17522493
|
G | GCC | 31 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0061others(28): Show | 31 | HG01074.hp1 HG01433.hp1 HG01515.hp1 others(28): Show |
intron_variant | MODIFIER | c.565+146183_565+146 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522493 | |||||
| chrX:17522493
|
G | GCCC | 15 | a0001c0001t0001g0081a0001c0001t0001g0140a0001c0001t0007g0102others(12): Show | 15 | HG00639.hp1 HG01192.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.565+146182_565+146 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522493 | |||||
| chrX:17522493
|
G | GCCCC | 10 | a0001c0001t0001g0104a0001c0001t0001g0129a0001c0001t0001g0145others(7): Show | 10 | HG00639.hp2 HG01099.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+146181_565+146 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522493 | |||||
| chrX:17522493
|
G | GCCCCC | 10 | a0001c0001t0001g0029a0001c0001t0001g0048a0001c0001t0001g0057others(7): Show | 10 | HG00609.hp1 HG02698.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+146180_565+146 others(11): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522493 | |||||
| chrX:17522493
|
G | GCCCCCC | 3 | a0001c0001t0001g0056a0001c0001t0001g0067a0002c0002t0001g0088 | 3 | HG02132.hp1 NA19060.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.565+146179_565+146 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522493 | |||||
| chrX:17522493
|
GC | G | 16 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0041others(13): Show | 16 | HG00408.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.565+146184delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522493 | |||||
| chrX:17522493
|
GCC | G | 3 | a0002c0002t0001g0016a0002c0002t0001g0017a0002c0002t0001g0030 | 3 | HG01975.hp2 NA19043.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.565+146183_565+146 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522493 | |||||
| chrX:17522493
|
GCCC | G | 1 | a0001c0001t0002g0106 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.565+146182_565+146 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522493 | |||||
| chrX:17522493
|
GCCCC | G | 4 | a0001c0001t0002g0107a0001c0001t0002g0110a0001c0001t0002g0164others(1): Show | 4 | HG02055.hp1 HG02717.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+146181_565+146 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522493 | |||||
| chrX:17522498
|
C | CCCCG | 1 | a0001c0001t0001g0133 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.565+146179_565+146 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522498 | |||||
| chrX:17522498
|
C | CCCG | 1 | a0001c0001t0001g0050 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.565+146178_565+146 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522498 | |||||
| chrX:17522499
|
C | CCG | 1 | a0001c0001t0001g0049 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.565+146178_565+146 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522499 | |||||
| chrX:17522501
|
C | A | 5 | a0001c0001t0002g0004a0001c0001t0002g0093a0001c0001t0002g0096others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+146179C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17522501 | ||||||
| chrX:17522502
|
C | A | 5 | a0001c0001t0002g0004a0001c0001t0002g0093a0001c0001t0002g0096others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+146180C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17522502 | ||||||
| chrX:17522502
|
C | G | 1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.565+146180C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17522502 | ||||||
| chrX:17522513
|
T | TC | 1 | a0002c0002t0001g0042 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.565+146198dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522513 | |||||
| chrX:17522623
|
G | C | 18 | a0001c0001t0002g0085a0001c0001t0002g0106a0001c0001t0002g0107others(15): Show | 18 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.565+146301G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17522623 | ||||||
| chrX:17522671
|
G | GC | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.565+146350dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522671 | |||||
| chrX:17522744
|
TGGCCTGT others(3): Show |
T | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+146424_565+146 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522744 | |||||
| chrX:17523116
|
A | T | 1 | a0001c0001t0002g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.565+146794A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17523116 | ||||||
| chrX:17523251
|
G | A | 1 | a0002c0002t0001g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.565+146929G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17523251 | ||||||
| chrX:17523359
|
G | T | 5 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+147037G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17523359 | ||||||
| chrX:17523510
|
G | A | 5 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+147188G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17523510 | ||||||
| chrX:17523716
|
T | TC | 163 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(160): Show | 163 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.565+147397dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17523716 | |||||
| chrX:17523716
|
T | TCCCCTCA others(45): Show |
1 | a0002c0002t0001g0024 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.565+147397_565+147 others(58): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17523716 | |||||
| chrX:17523914
|
A | G | 1 | a0005c0006t0008g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565+147592A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17523914 | ||||||
| chrX:17523943
|
G | A | 5 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+147621G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17523943 | ||||||
| chrX:17524045
|
G | GC | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+147726dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17524045 | |||||
| chrX:17524061
|
A | ATTTGTCT others(17): Show |
1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+147739_565+147 others(30): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17524061 | ||||||
| chrX:17524062
|
C | A | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+147740C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17524062 | ||||||
| chrX:17524077
|
G | A | 18 | a0001c0001t0002g0085a0001c0001t0002g0106a0001c0001t0002g0107others(15): Show | 18 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.565+147755G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17524077 | ||||||
| chrX:17524208
|
AT | A | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+147889delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17524208 | |||||
| chrX:17524222
|
T | TC | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+147905dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17524222 | |||||
| chrX:17524295
|
CA | C | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+147976delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17524295 | |||||
| chrX:17524307
|
A | AC | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+147989dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17524307 | |||||
| chrX:17524307
|
AC | A | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+147989delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17524307 | |||||
| chrX:17524424
|
A | G | 9 | a0001c0001t0002g0085a0001c0001t0005g0111a0001c0003t0002g0101others(6): Show | 9 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+148102A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17524424 | ||||||
| chrX:17524461
|
TC | T | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148142delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17524461 | |||||
| chrX:17524472
|
AT | A | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148153delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17524472 | |||||
| chrX:17524481
|
T | C | 9 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.565+148159T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17524481 | ||||||
| chrX:17524495
|
TC | T | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148177delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17524495 | |||||
| chrX:17524514
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148192G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17524514 | ||||||
| chrX:17524515
|
T | G | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148193T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17524515 | ||||||
| chrX:17524550
|
AT | A | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148233delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17524550 | |||||
| chrX:17524598
|
TG | T | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148278delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17524598 | |||||
| chrX:17524621
|
AT | A | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148302delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17524621 | |||||
| chrX:17524813
|
GA | G | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148493delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17524813 | |||||
| chrX:17524831
|
T | TA | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148509_565+148 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17524831 | ||||||
| chrX:17524891
|
CT | C | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148571delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17524891 | |||||
| chrX:17524925
|
T | A | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148603T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17524925 | ||||||
| chrX:17525019
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.565+148697G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525019 | ||||||
| chrX:17525026
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0090 | 2 | NA18967.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.565+148704G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525026 | ||||||
| chrX:17525028
|
G | GC | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+148708dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525028 | |||||
| chrX:17525063
|
C | CT | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+148745dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525063 | |||||
| chrX:17525095
|
GT | G | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148777delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525095 | |||||
| chrX:17525105
|
A | AT | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148784dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525105 | |||||
| chrX:17525106
|
T | C | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+148784T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525106 | ||||||
| chrX:17525135
|
T | G | 19 | a0001c0001t0002g0085a0001c0001t0002g0106a0001c0001t0002g0107others(16): Show | 19 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.565+148813T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525135 | ||||||
| chrX:17525171
|
T | TG | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148849_565+148 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525171 | ||||||
| chrX:17525234
|
G | GA | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+148916dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525234 | |||||
| chrX:17525234
|
GA | G | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148916delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525234 | |||||
| chrX:17525243
|
A | AC | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+148923dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525243 | |||||
| chrX:17525251
|
C | CT | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148933dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525251 | |||||
| chrX:17525322
|
AC | A | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149003delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525322 | |||||
| chrX:17525338
|
AG | A | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149019delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525338 | |||||
| chrX:17525357
|
T | C | 1 | a0006c0007t0002g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.565+149035T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525357 | ||||||
| chrX:17525359
|
GT | G | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149040delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525359 | |||||
| chrX:17525392
|
AG | A | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149072delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525392 | |||||
| chrX:17525450
|
T | G | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.565+149128T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525450 | ||||||
| chrX:17525465
|
TG | T | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149146delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525465 | |||||
| chrX:17525517
|
GT | G | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149202delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525517 | |||||
| chrX:17525542
|
C | CA | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+149224dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525542 | |||||
| chrX:17525542
|
CA | C | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149224delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525542 | |||||
| chrX:17525619
|
TTTC | T | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149300_565+149 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525619 | |||||
| chrX:17525624
|
T | C | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149302T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525624 | ||||||
| chrX:17525630
|
TTTC | T | 3 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110 | 3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+149311_565+149 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525630 | |||||
| chrX:17525638
|
C | CT | 26 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0098others(23): Show | 26 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.565+149337dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525638 | |||||
| chrX:17525638
|
C | CTT | 10 | a0001c0001t0002g0085a0001c0001t0002g0120a0001c0003t0002g0101others(7): Show | 10 | HG00642.hp1 HG02145.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+149336_565+149 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525638 | |||||
| chrX:17525638
|
C | CTTT | 1 | a0001c0001t0005g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.565+149335_565+149 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525638 | |||||
| chrX:17525638
|
CT | C | 7 | a0001c0001t0001g0104a0001c0001t0002g0093a0001c0001t0002g0106others(4): Show | 7 | HG01069.hp1 HG02258.hp1 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+149337delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525638 | |||||
| chrX:17525638
|
CTTT | C | 2 | a0001c0001t0002g0164a0004c0005t0003g0100 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.565+149335_565+149 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525638 | |||||
| chrX:17525668
|
G | A | 1 | a0002c0002t0001g0062 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.565+149346G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525668 | ||||||
| chrX:17525682
|
TG | T | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149363delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525682 | |||||
| chrX:17525734
|
GT | G | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149416delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525734 | |||||
| chrX:17525759
|
G | C | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149437G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525759 | ||||||
| chrX:17525760
|
C | G | 2 | a0001c0001t0002g0093a0001c0001t0002g0143 | 2 | HG01069.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.565+149438C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525760 | ||||||
| chrX:17525787
|
G | C | 2 | a0001c0001t0002g0164a0004c0005t0003g0100 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.565+149465G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525787 | ||||||
| chrX:17525794
|
TG | T | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149477delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525794 | |||||
| chrX:17525843
|
G | T | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149521G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525843 | ||||||
| chrX:17525845
|
T | G | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149523T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525845 | ||||||
| chrX:17525987
|
CT | C | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149668delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525987 | |||||
| chrX:17526010
|
TG | T | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149690delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17526010 | |||||
| chrX:17526069
|
CA | C | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149750delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17526069 | |||||
| chrX:17526080
|
C | CA | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+149763dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17526080 | |||||
| chrX:17526156
|
C | T | 5 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+149834C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17526156 | ||||||
| chrX:17526178
|
A | AC | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+149860dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17526178 | |||||
| chrX:17526178
|
AC | A | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149860delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17526178 | |||||
| chrX:17526239
|
G | T | 13 | a0001c0001t0002g0085a0001c0001t0002g0116a0001c0001t0002g0120others(10): Show | 13 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.565+149917G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17526239 | ||||||
| chrX:17526311
|
T | C | 28 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0061others(25): Show | 28 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.565+149989T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17526311 | ||||||
| chrX:17526377
|
C | G | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.565+150055C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17526377 | ||||||
| chrX:17526381
|
T | C | 1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.565+150059T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17526381 | ||||||
| chrX:17526414
|
G | T | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.565+150092G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17526414 | ||||||
| chrX:17526658
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.565+150336A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17526658 | ||||||
| chrX:17527225
|
T | C | 1 | a0001c0001t0017g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.565+150903T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17527225 | ||||||
| chrX:17527249
|
T | C | 29 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0061others(26): Show | 29 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.565+150927T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17527249 | ||||||
| chrX:17527413
|
A | G | 2 | a0001c0001t0002g0164a0004c0005t0003g0100 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.565+151091A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17527413 | ||||||
| chrX:17527776
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.565+151454T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17527776 | ||||||
| chrX:17527918
|
T | TG | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.565+151597dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17527918 | |||||
| chrX:17528367
|
A | G | 9 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.565+152045A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17528367 | ||||||
| chrX:17528503
|
G | A | 1 | a0002c0002t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.565+152181G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17528503 | ||||||
| chrX:17528673
|
C | T | 4 | a0001c0001t0002g0093a0001c0001t0002g0096a0001c0001t0002g0126others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+152351C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17528673 | ||||||
| chrX:17528675
|
CGCTGTGT others(9): Show |
C | 2 | a0001c0003t0002g0142a0001c0003t0002g0155 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.565+152354_565+152 others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17528675 | ||||||
| chrX:17528880
|
C | T | 1 | a0002c0002t0001g0024 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.565+152558C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17528880 | ||||||
| chrX:17528881
|
G | A | 19 | a0001c0001t0002g0085a0001c0001t0002g0106a0001c0001t0002g0107others(16): Show | 19 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.565+152559G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17528881 | ||||||
| chrX:17529262
|
C | T | 29 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0061others(26): Show | 29 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.565+152940C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17529262 | ||||||
| chrX:17529527
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+153205G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17529527 | ||||||
| chrX:17529621
|
A | G | 13 | a0001c0001t0002g0085a0001c0001t0002g0116a0001c0001t0002g0120others(10): Show | 13 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.565+153299A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17529621 | ||||||
| chrX:17529974
|
T | G | 1 | a0001c0001t0002g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.565+153652T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17529974 | ||||||
| chrX:17530192
|
A | G | 1 | a0002c0002t0001g0040 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.565+153870A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17530192 | ||||||
| chrX:17530709
|
T | C | 7 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(4): Show | 7 | HG02258.hp1 HG03098.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+154387T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17530709 | ||||||
| chrX:17530856
|
G | A | 13 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0057others(10): Show | 13 | HG00408.hp2 HG00609.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.565+154534G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17530856 | ||||||
| chrX:17530942
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.565+154620C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17530942 | ||||||
| chrX:17531112
|
A | G | 4 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0006g0112others(1): Show | 4 | HG03098.hp1 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+154790A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17531112 | ||||||
| chrX:17531144
|
C | G | 9 | a0001c0001t0002g0085a0001c0001t0005g0111a0001c0003t0002g0101others(6): Show | 9 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+154822C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17531144 | ||||||
| chrX:17531323
|
G | C | 71 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0036others(68): Show | 71 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.565+155001G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17531323 | ||||||
| chrX:17531817
|
A | G | 7 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(4): Show | 7 | HG02258.hp1 HG03098.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+155495A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17531817 | ||||||
| chrX:17532031
|
C | T | 16 | a0001c0001t0002g0085a0001c0001t0002g0106a0001c0001t0002g0107others(13): Show | 16 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.565+155709C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17532031 | ||||||
| chrX:17532343
|
C | T | 1 | a0004c0005t0003g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.566-155399C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17532343 | ||||||
| chrX:17532853
|
T | G | 54 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0036others(51): Show | 54 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.566-154889T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17532853 | ||||||
| chrX:17533006
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.566-154736G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17533006 | ||||||
| chrX:17533069
|
A | G | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.566-154673A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17533069 | ||||||
| chrX:17533210
|
G | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.566-154532G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17533210 | ||||||
| chrX:17533443
|
C | T | 1 | a0001c0001t0004g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.566-154299C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17533443 | ||||||
| chrX:17533445
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.566-154297C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17533445 | ||||||
| chrX:17533537
|
T | G | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.566-154205T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17533537 | ||||||
| chrX:17533543
|
T | C | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.566-154199T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17533543 | ||||||
| chrX:17533569
|
A | G | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.566-154173A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17533569 | ||||||
| chrX:17533576
|
G | C | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.566-154166G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17533576 | ||||||
| chrX:17533649
|
AC | A | 12 | a0001c0001t0002g0085a0001c0001t0002g0106a0001c0001t0002g0107others(9): Show | 12 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-154092delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17533649 | ||||||
| chrX:17533883
|
A | G | 16 | a0001c0001t0002g0085a0001c0001t0002g0106a0001c0001t0002g0107others(13): Show | 16 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.566-153859A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17533883 | ||||||
| chrX:17534096
|
T | TTG | 6 | a0001c0001t0002g0096a0002c0002t0001g0023a0002c0002t0001g0024others(3): Show | 6 | HG02015.hp1 HG02027.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-153621_566-153 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17534096 | |||||
| chrX:17534096
|
T | TTGTG | 25 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0057others(22): Show | 25 | HG00408.hp2 HG00609.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-153623_566-153 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17534096 | |||||
| chrX:17534096
|
T | TTGTGTG | 83 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0038others(80): Show | 83 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.566-153625_566-153 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17534096 | |||||
| chrX:17534096
|
T | TTGTGTGT others(1): Show |
9 | a0001c0001t0002g0099a0001c0001t0002g0143a0001c0001t0002g0146others(6): Show | 9 | HG01243.hp1 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.566-153627_566-153 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17534096 | |||||
| chrX:17534096
|
T | TTGTGTGT others(3): Show |
1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.566-153629_566-153 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17534096 | |||||
| chrX:17534527
|
G | A | 67 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0036others(64): Show | 67 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.566-153215G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17534527 | ||||||
| chrX:17534595
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.566-153147G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17534595 | ||||||
| chrX:17534845
|
T | A | 1 | a0001c0001t0009g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.566-152897T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17534845 | ||||||
| chrX:17534983
|
C | A | 1 | a0001c0001t0004g0058 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.566-152759C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17534983 | ||||||
| chrX:17535283
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0090 | 2 | NA18967.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.566-152459G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17535283 | ||||||
| chrX:17535659
|
A | G | 19 | a0001c0001t0002g0085a0001c0001t0002g0106a0001c0001t0002g0107others(16): Show | 19 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.566-152083A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17535659 | ||||||
| chrX:17535792
|
G | C | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.566-151950G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17535792 | ||||||
| chrX:17536179
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.566-151563C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536179 | ||||||
| chrX:17536215
|
C | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0074 | 2 | HG01358.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.566-151527C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536215 | ||||||
| chrX:17536256
|
G | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.566-151486G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536256 | ||||||
| chrX:17536260
|
C | A | 12 | a0001c0001t0002g0085a0001c0001t0002g0106a0001c0001t0002g0107others(9): Show | 12 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-151482C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536260 | ||||||
| chrX:17536310
|
G | A | 9 | a0001c0001t0002g0085a0001c0001t0005g0111a0001c0003t0002g0101others(6): Show | 9 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.566-151432G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536310 | ||||||
| chrX:17536354
|
C | CA | 6 | a0001c0001t0001g0026a0002c0002t0001g0001a0002c0002t0001g0015others(3): Show | 6 | HG02083.hp1 NA18747.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-151381dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17536354 | |||||
| chrX:17536358
|
AAAAC | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0090 | 2 | NA18967.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.566-151372_566-151 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17536358 | |||||
| chrX:17536373
|
AAAACAAA others(1): Show |
A | 1 | a0002c0002t0001g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.566-151357_566-151 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17536373 | |||||
| chrX:17536474
|
C | T | 13 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0057others(10): Show | 13 | HG00408.hp2 HG00609.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.566-151268C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536474 | ||||||
| chrX:17536481
|
C | G | 1 | a0002c0002t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.566-151261C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536481 | ||||||
| chrX:17536502
|
T | C | 1 | a0004c0005t0003g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.566-151240T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536502 | ||||||
| chrX:17536521
|
A | G | 3 | a0002c0002t0001g0025a0003c0004t0001g0149a0010c0012t0001g0150 | 3 | NA18948.hp1 NA18990.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.566-151221A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536521 | ||||||
| chrX:17536564
|
G | T | 1 | a0002c0002t0001g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.566-151178G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536564 | ||||||
| chrX:17536746
|
C | G | 3 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110 | 3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.566-150996C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536746 | ||||||
| chrX:17536749
|
C | T | 3 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110 | 3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.566-150993C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536749 | ||||||
| chrX:17536799
|
C | A | 1 | a0001c0001t0001g0135 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.566-150943C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536799 | ||||||
| chrX:17537036
|
C | G | 1 | a0003c0004t0001g0013 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.566-150706C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17537036 | ||||||
| chrX:17537109
|
A | G | 2 | a0001c0001t0001g0137a0001c0001t0012g0044 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.566-150633A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17537109 | ||||||
| chrX:17537167
|
C | T | 16 | a0001c0001t0001g0068a0001c0001t0002g0085a0001c0001t0002g0106others(13): Show | 16 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.566-150575C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17537167 | ||||||
| chrX:17537249
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.566-150493G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17537249 | ||||||
| chrX:17537869
|
C | T | 1 | a0002c0002t0001g0008 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.566-149873C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17537869 | ||||||
| chrX:17537966
|
A | G | 2 | a0001c0001t0006g0112a0009c0011t0002g0147 | 2 | HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.566-149776A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17537966 | ||||||
| chrX:17538176
|
G | C | 1 | a0001c0001t0005g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.566-149566G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17538176 | ||||||
| chrX:17538492
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.566-149250T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17538492 | ||||||
| chrX:17538751
|
C | T | 1 | a0002c0002t0001g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.566-148991C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17538751 | ||||||
| chrX:17538754
|
G | GA | 1 | a0002c0002t0001g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.566-148985dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17538754 | |||||
| chrX:17538851
|
G | A | 11 | a0001c0001t0002g0099a0001c0001t0002g0116a0001c0001t0002g0120others(8): Show | 11 | HG01243.hp1 HG02257.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-148891G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17538851 | ||||||
| chrX:17538906
|
T | C | 2 | a0002c0002t0001g0037a0002c0002t0001g0075 | 2 | HG04228.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.566-148836T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17538906 | ||||||
| chrX:17539017
|
G | A | 1 | a0013c0016t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.566-148725G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17539017 | ||||||
| chrX:17539315
|
T | G | 1 | a0002c0002t0001g0007 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.566-148427T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17539315 | ||||||
| chrX:17539548
|
A | C | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.566-148194A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17539548 | ||||||
| chrX:17539549
|
C | A | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.566-148193C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17539549 | ||||||
| chrX:17539964
|
G | C | 2 | a0001c0001t0002g0002a0001c0001t0002g0164 | 2 | HG02293.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.566-147778G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17539964 | ||||||
| chrX:17540368
|
TG | T | 1 | a0001c0001t0001g0050 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.566-147371delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17540368 | |||||
| chrX:17540601
|
G | A | 2 | a0001c0001t0002g0002a0001c0001t0002g0164 | 2 | HG02293.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.566-147141G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17540601 | ||||||
| chrX:17540656
|
AC | A | 1 | a0001c0001t0001g0050 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.566-147083delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17540656 | |||||
| chrX:17540778
|
G | A | 2 | a0005c0006t0001g0162a0005c0006t0008g0161 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.566-146964G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17540778 | ||||||
| chrX:17540850
|
C | T | 1 | a0013c0016t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.566-146892C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17540850 | ||||||
| chrX:17540889
|
G | A | 3 | a0001c0001t0001g0052a0002c0002t0001g0051a0002c0002t0016g0005 | 3 | HG00621.hp1 NA18612.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.566-146853G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17540889 | ||||||
| chrX:17541082
|
TA | T | 5 | a0001c0003t0002g0128a0001c0003t0002g0142a0001c0003t0002g0155others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-146650delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541082 | |||||
| chrX:17541093
|
T | A | 3 | a0005c0006t0001g0157a0006c0008t0001g0114a0013c0016t0002g0119 | 3 | HG01106.hp1 HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.566-146649T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17541093 | ||||||
| chrX:17541187
|
T | C | 115 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(112): Show | 115 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.566-146555T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17541187 | ||||||
| chrX:17541462
|
G | T | 5 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0009g0122others(2): Show | 5 | HG02257.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-146280G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17541462 | ||||||
| chrX:17541561
|
A | G | 1 | a0001c0003t0002g0019 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.566-146181A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17541561 | ||||||
| chrX:17541767
|
A | AAC | 11 | a0001c0001t0001g0050a0001c0001t0001g0083a0001c0001t0001g0129others(8): Show | 11 | HG01099.hp1 HG01255.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.566-145928_566-145 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | |||||
| chrX:17541767
|
A | AACAC | 12 | a0001c0001t0001g0026a0001c0001t0002g0116a0001c0001t0004g0058others(9): Show | 12 | HG00140.hp1 HG02027.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-145930_566-145 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | |||||
| chrX:17541767
|
A | AACACAC | 3 | a0001c0001t0001g0068a0002c0002t0001g0033a0008c0010t0003g0158 | 3 | HG01192.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.566-145932_566-145 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | |||||
| chrX:17541767
|
A | AACACACA others(1): Show |
8 | a0001c0001t0002g0110a0001c0001t0002g0120a0001c0001t0002g0146others(5): Show | 8 | HG02630.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-145934_566-145 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | |||||
| chrX:17541767
|
A | AACACACA others(3): Show |
8 | a0001c0001t0001g0022a0001c0001t0002g0106a0001c0001t0002g0107others(5): Show | 8 | HG02135.hp1 HG02258.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-145936_566-145 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | |||||
| chrX:17541767
|
A | AACACACA others(5): Show |
13 | a0001c0001t0001g0048a0001c0001t0001g0057a0001c0001t0001g0145others(10): Show | 13 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.566-145938_566-145 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | |||||
| chrX:17541767
|
A | AACACACA others(7): Show |
20 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0002g0121others(17): Show | 20 | HG00673.hp1 HG01167.hp1 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.566-145940_566-145 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | |||||
| chrX:17541767
|
A | AACACACA others(9): Show |
18 | a0001c0001t0002g0004a0001c0001t0002g0096a0001c0001t0004g0163others(15): Show | 18 | HG01261.hp1 HG01515.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.566-145942_566-145 others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | |||||
| chrX:17541767
|
A | AACACACA others(11): Show |
15 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0081others(12): Show | 15 | HG01258.hp1 HG02015.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-145944_566-145 others(24): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | |||||
| chrX:17541767
|
A | AACACACA others(13): Show |
11 | a0001c0001t0001g0029a0001c0001t0001g0137a0001c0001t0001g0144others(8): Show | 11 | HG01069.hp1 HG01071.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.566-145946_566-145 others(26): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | |||||
| chrX:17541767
|
A | AACACACA others(15): Show |
3 | a0001c0001t0001g0095a0002c0015t0001g0046a0005c0006t0001g0157 | 3 | HG01106.hp1 NA18522.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.566-145948_566-145 others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | |||||
| chrX:17541767
|
A | AACACACA others(17): Show |
1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.566-145950_566-145 others(30): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | |||||
| chrX:17541767
|
AAC | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0056a0001c0001t0002g0043others(1): Show | 4 | HG01074.hp1 HG01109.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-145928_566-145 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | |||||
| chrX:17541767
|
AACAC | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0049others(1): Show | 4 | HG02071.hp1 NA18961.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-145930_566-145 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | |||||
| chrX:17541767
|
AACACACA others(1): Show |
A | 1 | a0001c0001t0001g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.566-145934_566-145 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | |||||
| chrX:17541814
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0002g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.566-145927_566-145 others(17): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541814 | |||||
| chrX:17541847
|
A | G | 7 | a0001c0001t0002g0002a0001c0001t0002g0164a0001c0003t0002g0128others(4): Show | 7 | HG02280.hp2 HG02293.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-145895A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17541847 | ||||||
| chrX:17541930
|
T | C | 105 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(102): Show | 105 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.566-145812T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17541930 | ||||||
| chrX:17542246
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.566-145496C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17542246 | ||||||
| chrX:17542276
|
T | C | 10 | a0001c0001t0002g0002a0001c0001t0002g0164a0001c0003t0002g0128others(7): Show | 10 | HG01106.hp1 HG02280.hp2 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.566-145466T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17542276 | ||||||
| chrX:17542278
|
C | T | 2 | a0001c0001t0012g0044a0004c0005t0010g0086 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.566-145464C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17542278 | ||||||
| chrX:17542329
|
G | A | 2 | a0005c0006t0001g0157a0006c0008t0001g0114 | 2 | HG01106.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.566-145413G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17542329 | ||||||
| chrX:17542689
|
C | CAG | 14 | a0001c0001t0002g0002a0001c0001t0002g0085a0001c0001t0002g0164others(11): Show | 14 | HG01106.hp1 HG02293.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.566-145029_566-145 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17542689 | |||||
| chrX:17542689
|
C | CAGAG | 2 | a0001c0001t0001g0041a0001c0003t0002g0128 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.566-145031_566-145 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17542689 | |||||
| chrX:17542719
|
G | A | 1 | a0004c0005t0010g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.566-145023G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17542719 | ||||||
| chrX:17542854
|
C | T | 100 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(97): Show | 100 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.566-144888C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17542854 | ||||||
| chrX:17543182
|
C | T | 8 | a0001c0003t0002g0128a0001c0003t0002g0142a0001c0003t0002g0155others(5): Show | 8 | HG01106.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-144560C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17543182 | ||||||
| chrX:17543238
|
C | G | 2 | a0005c0006t0001g0157a0013c0016t0002g0119 | 2 | HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.566-144504C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17543238 | ||||||
| chrX:17543279
|
A | G | 10 | a0001c0001t0002g0002a0001c0001t0002g0164a0001c0003t0002g0128others(7): Show | 10 | HG01106.hp1 HG02280.hp2 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.566-144463A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17543279 | ||||||
| chrX:17543356
|
A | G | 2 | a0002c0002t0001g0021a0002c0002t0001g0034 | 2 | HG00280.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.566-144386A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17543356 | ||||||
| chrX:17543638
|
GT | G | 2 | a0005c0006t0001g0157a0013c0016t0002g0119 | 2 | HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.566-144096delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17543638 | |||||
| chrX:17543791
|
G | A | 1 | a0001c0001t0013g0059 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.566-143951G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17543791 | ||||||
| chrX:17543832
|
C | T | 1 | a0002c0002t0001g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.566-143910C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17543832 | ||||||
| chrX:17543877
|
G | T | 2 | a0005c0006t0001g0157a0013c0016t0002g0119 | 2 | HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.566-143865G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17543877 | ||||||
| chrX:17544634
|
T | C | 2 | a0001c0001t0002g0002a0001c0001t0002g0164 | 2 | HG02293.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.566-143108T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17544634 | ||||||
| chrX:17545297
|
T | C | 6 | a0001c0003t0002g0128a0001c0003t0002g0142a0001c0003t0002g0155others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-142445T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545297 | ||||||
| chrX:17545311
|
G | A | 8 | a0001c0001t0001g0127a0001c0001t0002g0106a0001c0001t0002g0107others(5): Show | 8 | HG01071.hp2 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-142431G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545311 | ||||||
| chrX:17545374
|
G | A | 10 | a0001c0001t0002g0002a0001c0001t0002g0164a0001c0003t0002g0128others(7): Show | 10 | HG01106.hp1 HG02280.hp2 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.566-142368G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545374 | ||||||
| chrX:17545453
|
G | A | 2 | a0001c0001t0001g0050a0002c0002t0001g0156 | 2 | NA18974.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.566-142289G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545453 | ||||||
| chrX:17545496
|
A | G | 8 | a0001c0001t0002g0002a0001c0001t0002g0164a0001c0003t0002g0128others(5): Show | 8 | HG02280.hp2 HG02293.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-142246A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545496 | ||||||
| chrX:17545513
|
T | A | 2 | a0005c0006t0001g0157a0013c0016t0002g0119 | 2 | HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.566-142229T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545513 | ||||||
| chrX:17545627
|
T | C | 2 | a0001c0001t0002g0002a0001c0001t0002g0164 | 2 | HG02293.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.566-142115T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545627 | ||||||
| chrX:17545646
|
G | A | 2 | a0005c0006t0001g0157a0013c0016t0002g0119 | 2 | HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.566-142096G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545646 | ||||||
| chrX:17545881
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.566-141861A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545881 | ||||||
| chrX:17545915
|
C | A | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.566-141827C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545915 | ||||||
| chrX:17546126
|
G | C | 6 | a0001c0003t0002g0128a0001c0003t0002g0142a0001c0003t0002g0155others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-141616G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17546126 | ||||||
| chrX:17546207
|
C | T | 1 | a0001c0001t0006g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.566-141535C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17546207 | ||||||
| chrX:17546308
|
G | A | 2 | a0002c0002t0001g0016a0002c0002t0001g0064 | 2 | HG03492.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.566-141434G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17546308 | ||||||
| chrX:17546346
|
G | A | 1 | a0002c0002t0001g0007 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.566-141396G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17546346 | ||||||
| chrX:17546382
|
A | T | 2 | a0002c0002t0001g0076a0002c0002t0001g0078 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.566-141360A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17546382 | ||||||
| chrX:17546594
|
A | T | 8 | a0001c0001t0002g0002a0001c0001t0002g0164a0001c0003t0002g0128others(5): Show | 8 | HG02280.hp2 HG02293.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-141148A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17546594 | ||||||
| chrX:17546690
|
G | A | 1 | a0001c0001t0017g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.566-141052G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17546690 | ||||||
| chrX:17546787
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.566-140955G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17546787 | ||||||
| chrX:17546985
|
T | G | 1 | a0001c0001t0001g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.566-140757T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17546985 | ||||||
| chrX:17547119
|
A | G | 8 | a0001c0001t0002g0002a0001c0001t0002g0164a0001c0003t0002g0128others(5): Show | 8 | HG02280.hp2 HG02293.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-140623A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17547119 | ||||||
| chrX:17547276
|
A | G | 1 | a0002c0015t0001g0046 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.566-140466A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17547276 | ||||||
| chrX:17547821
|
C | T | 2 | a0001c0001t0001g0137a0004c0005t0003g0117 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.566-139921C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17547821 | ||||||
| chrX:17547856
|
T | C | 3 | a0005c0006t0001g0157a0006c0008t0001g0114a0013c0016t0002g0119 | 3 | HG01106.hp1 HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.566-139886T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17547856 | ||||||
| chrX:17547878
|
C | T | 2 | a0001c0001t0002g0002a0001c0001t0002g0164 | 2 | HG02293.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.566-139864C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17547878 | ||||||
| chrX:17548055
|
A | G | 1 | a0002c0002t0001g0031 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.566-139687A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17548055 | ||||||
| chrX:17548160
|
C | T | 7 | a0001c0001t0002g0002a0001c0001t0002g0164a0001c0003t0002g0128others(4): Show | 7 | HG02280.hp2 HG02293.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-139582C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17548160 | ||||||
| chrX:17548302
|
GT | G | 3 | a0001c0001t0001g0048a0002c0002t0001g0138a0002c0002t0001g0139 | 3 | HG00673.hp1 HG02074.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.566-139429delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17548302 | |||||
| chrX:17548586
|
G | A | 5 | a0001c0003t0002g0128a0001c0003t0002g0142a0001c0003t0002g0155others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-139156G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17548586 | ||||||
| chrX:17548837
|
G | A | 1 | a0002c0015t0001g0046 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.566-138905G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17548837 | ||||||
| chrX:17548859
|
C | A | 17 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0057others(14): Show | 17 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.566-138883C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17548859 | ||||||
| chrX:17549134
|
T | TA | 33 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0070others(30): Show | 33 | HG01071.hp2 HG01074.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.566-138592dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17549134 | |||||
| chrX:17549134
|
T | TAA | 3 | a0001c0001t0002g0004a0001c0001t0002g0096a0004c0005t0010g0097 | 3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.566-138593_566-138 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17549134 | |||||
| chrX:17549134
|
TA | T | 6 | a0001c0001t0001g0151a0001c0001t0002g0002a0001c0001t0004g0069others(3): Show | 6 | HG00408.hp1 HG01515.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-138592delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17549134 | |||||
| chrX:17549210
|
TGCCAGGC others(3): Show |
T | 44 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0048others(41): Show | 44 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-138525_566-138 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17549210 | |||||
| chrX:17549214
|
A | AG | 119 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(116): Show | 119 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.566-138526dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17549214 | |||||
| chrX:17549214
|
A | AGGGCCAG | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.566-138526_566-138 others(13): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17549214 | |||||
| chrX:17549219
|
A | AG | 120 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(117): Show | 120 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.566-138521dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17549219 | |||||
| chrX:17549484
|
T | C | 28 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0137others(25): Show | 28 | HG00408.hp2 HG01109.hp1 HG01258.hp1 others(25): Show |
intron_variant | MODIFIER | c.566-138258T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17549484 | ||||||
| chrX:17549515
|
G | A | 3 | a0001c0001t0001g0137a0001c0001t0002g0002a0004c0005t0003g0117 | 3 | HG02293.hp2 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.566-138227G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17549515 | ||||||
| chrX:17549558
|
GC | G | 1 | a0002c0002t0001g0007 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.566-138182delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17549558 | |||||
| chrX:17549577
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0049others(1): Show | 4 | HG02071.hp1 NA18961.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-138165G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17549577 | ||||||
| chrX:17549609
|
G | A | 2 | a0001c0001t0002g0099a0001c0001t0002g0143 | 2 | HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.566-138133G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17549609 | ||||||
| chrX:17549936
|
C | T | 85 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(82): Show | 85 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.566-137806C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17549936 | ||||||
| chrX:17550177
|
G | A | 12 | a0001c0001t0001g0127a0001c0001t0001g0137a0001c0001t0002g0002others(9): Show | 12 | HG01071.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-137565G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17550177 | ||||||
| chrX:17550288
|
A | G | 16 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(13): Show | 16 | HG01106.hp1 HG01109.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.566-137454A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17550288 | ||||||
| chrX:17550395
|
A | T | 85 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(82): Show | 85 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.566-137347A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17550395 | ||||||
| chrX:17550531
|
G | C | 3 | a0002c0002t0001g0076a0002c0002t0001g0131a0002c0002t0014g0063 | 3 | HG02602.hp1 HG03654.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.566-137211G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17550531 | ||||||
| chrX:17550897
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.566-136845C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17550897 | ||||||
| chrX:17551378
|
T | G | 5 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(2): Show | 5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-136364T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17551378 | ||||||
| chrX:17551763
|
C | T | 1 | a0008c0010t0003g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.566-135979C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17551763 | ||||||
| chrX:17551821
|
C | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.566-135921C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17551821 | ||||||
| chrX:17552008
|
G | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.566-135734G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552008 | ||||||
| chrX:17552031
|
GA | G | 46 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0048others(43): Show | 46 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.566-135710delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552031 | ||||||
| chrX:17552032
|
A | G | 44 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0057others(41): Show | 44 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-135710A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552032 | ||||||
| chrX:17552035
|
A | G | 46 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0048others(43): Show | 46 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.566-135707A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552035 | ||||||
| chrX:17552063
|
G | C | 6 | a0001c0001t0001g0041a0001c0001t0001g0068a0004c0005t0003g0117others(3): Show | 6 | HG01106.hp1 HG02145.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-135679G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552063 | ||||||
| chrX:17552079
|
G | C | 1 | a0002c0002t0001g0028 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.566-135663G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552079 | ||||||
| chrX:17552261
|
G | A | 73 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(70): Show | 73 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.566-135481G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552261 | ||||||
| chrX:17552710
|
G | A | 24 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(21): Show | 24 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.566-135032G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552710 | ||||||
| chrX:17552722
|
G | A | 14 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0099others(11): Show | 14 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.566-135020G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552722 | ||||||
| chrX:17552769
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.566-134973A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552769 | ||||||
| chrX:17552795
|
G | A | 86 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(83): Show | 86 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.566-134947G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552795 | ||||||
| chrX:17552864
|
T | G | 80 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(77): Show | 80 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.566-134878T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552864 | ||||||
| chrX:17553002
|
C | A | 1 | a0002c0002t0001g0014 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.566-134740C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17553002 | ||||||
| chrX:17553036
|
T | A | 90 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(87): Show | 90 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.566-134706T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17553036 | ||||||
| chrX:17553072
|
G | A | 1 | a0006c0007t0002g0118 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.566-134670G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17553072 | ||||||
| chrX:17553118
|
C | T | 1 | a0001c0001t0006g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.566-134624C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17553118 | ||||||
| chrX:17553174
|
C | T | 2 | a0001c0003t0002g0142a0006c0007t0002g0115 | 2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.566-134568C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17553174 | ||||||
| chrX:17553259
|
AAG | A | 7 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0002g0043others(4): Show | 7 | HG01106.hp1 HG01109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-134481_566-134 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17553259 | |||||
| chrX:17553320
|
T | C | 1 | a0002c0002t0011g0020 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.566-134422T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17553320 | ||||||
| chrX:17553628
|
G | GA | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.566-134106dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17553628 | |||||
| chrX:17553759
|
C | T | 6 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-133983C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17553759 | ||||||
| chrX:17553795
|
C | G | 25 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(22): Show | 25 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-133947C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17553795 | ||||||
| chrX:17553957
|
G | C | 91 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(88): Show | 91 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.566-133785G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17553957 | ||||||
| chrX:17554269
|
G | A | 6 | a0001c0001t0001g0041a0001c0001t0001g0068a0004c0005t0003g0117others(3): Show | 6 | HG01106.hp1 HG02145.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-133473G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17554269 | ||||||
| chrX:17554405
|
G | A | 11 | a0001c0001t0001g0127a0001c0001t0001g0137a0001c0001t0002g0002others(8): Show | 11 | HG01928.hp1 HG01952.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-133337G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17554405 | ||||||
| chrX:17554407
|
AG | A | 11 | a0001c0001t0001g0127a0001c0001t0001g0137a0001c0001t0002g0002others(8): Show | 11 | HG01928.hp1 HG01952.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-133329delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17554407 | |||||
| chrX:17554843
|
C | CT | 25 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(22): Show | 25 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-132890dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17554843 | |||||
| chrX:17555118
|
C | T | 2 | a0002c0002t0001g0008a0002c0002t0001g0040 | 2 | HG01167.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.566-132624C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17555118 | ||||||
| chrX:17555228
|
AT | A | 12 | a0001c0001t0001g0081a0001c0001t0002g0096a0001c0001t0002g0106others(9): Show | 12 | HG01071.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-132498delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17555228 | |||||
| chrX:17555296
|
CT | C | 1 | a0008c0010t0003g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.566-132445delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17555296 | ||||||
| chrX:17555306
|
G | A | 25 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(22): Show | 25 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-132436G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17555306 | ||||||
| chrX:17555308
|
G | A | 4 | a0001c0001t0012g0044a0001c0001t0017g0154a0004c0005t0010g0086others(1): Show | 4 | HG01975.hp1 HG02257.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-132434G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17555308 | ||||||
| chrX:17555328
|
T | C | 116 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(113): Show | 116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.566-132414T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17555328 | ||||||
| chrX:17555638
|
T | C | 1 | a0013c0016t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.566-132104T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17555638 | ||||||
| chrX:17555782
|
C | T | 80 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(77): Show | 80 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.566-131960C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17555782 | ||||||
| chrX:17555900
|
A | AG | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.566-131841dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17555900 | |||||
| chrX:17555961
|
A | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.566-131781A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17555961 | ||||||
| chrX:17556162
|
C | T | 18 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(15): Show | 18 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.566-131580C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17556162 | ||||||
| chrX:17556470
|
TA | T | 34 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(31): Show | 34 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.566-131269delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17556470 | |||||
| chrX:17556650
|
G | C | 35 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(32): Show | 35 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.566-131092G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17556650 | ||||||
| chrX:17556740
|
A | G | 5 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(2): Show | 5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-131002A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17556740 | ||||||
| chrX:17556772
|
G | A | 163 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(160): Show | 163 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.566-130970G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17556772 | ||||||
| chrX:17556973
|
G | GAT | 37 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(34): Show | 37 | HG00408.hp2 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.566-130756_566-130 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17556973 | |||||
| chrX:17557108
|
TTTGTGTG others(2): Show |
T | 1 | a0001c0001t0002g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.566-130632_566-130 others(15): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557108 | |||||
| chrX:17557109
|
T | TTG | 21 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0002g0121others(18): Show | 21 | HG00280.hp1 HG00408.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.566-130591_566-130 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | |||||
| chrX:17557109
|
T | TTGTG | 3 | a0001c0001t0004g0163a0002c0002t0001g0018a0002c0002t0001g0080 | 3 | HG01074.hp1 HG01261.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.566-130593_566-130 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | |||||
| chrX:17557109
|
T | TTGTGTG | 6 | a0001c0001t0002g0043a0002c0002t0001g0024a0002c0002t0001g0087others(3): Show | 6 | HG01109.hp1 HG02922.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-130595_566-130 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | |||||
| chrX:17557109
|
T | TTGTGTGT others(1): Show |
1 | a0001c0001t0001g0127 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.566-130597_566-130 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | |||||
| chrX:17557109
|
TTG | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0001g0068others(7): Show | 10 | HG01358.hp1 HG01515.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-130591_566-130 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | |||||
| chrX:17557109
|
TTGTG | T | 6 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0003t0002g0128others(3): Show | 6 | HG01106.hp1 HG01256.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-130593_566-130 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | |||||
| chrX:17557109
|
TTGTGTG | T | 20 | a0001c0001t0002g0085a0001c0001t0002g0096a0001c0001t0002g0106others(17): Show | 20 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.566-130595_566-130 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | |||||
| chrX:17557109
|
TTGTGTGT others(1): Show |
T | 4 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0009g0122others(1): Show | 4 | HG02615.hp2 HG02723.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-130597_566-130 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | |||||
| chrX:17557109
|
TTGTGTGT others(3): Show |
T | 6 | a0001c0001t0002g0099a0001c0001t0002g0146a0001c0001t0012g0044others(3): Show | 6 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-130599_566-130 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | |||||
| chrX:17557109
|
TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.566-130603_566-130 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | |||||
| chrX:17557109
|
TTGTGTGT others(13): Show |
T | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.566-130609_566-130 others(26): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | |||||
| chrX:17557196
|
A | C | 108 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0041others(105): Show | 108 | HG00280.hp1 HG00408.hp2 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.566-130546A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17557196 | ||||||
| chrX:17557326
|
G | GAT | 11 | a0001c0001t0002g0085a0001c0001t0002g0121a0001c0001t0005g0103others(8): Show | 11 | HG00738.hp1 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-130395_566-130 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557326 | |||||
| chrX:17557326
|
G | GATAT | 9 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(6): Show | 9 | HG00639.hp1 HG01106.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-130397_566-130 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557326 | |||||
| chrX:17557326
|
G | GATATAT | 14 | a0001c0001t0002g0096a0001c0001t0002g0106a0001c0001t0002g0107others(11): Show | 14 | HG00408.hp2 HG01071.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.566-130399_566-130 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557326 | |||||
| chrX:17557326
|
G | GATATATA others(1): Show |
5 | a0001c0001t0009g0125a0002c0002t0001g0072a0003c0004t0001g0132others(2): Show | 5 | HG01952.hp1 HG02055.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-130401_566-130 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557326 | |||||
| chrX:17557326
|
G | GATATATA others(3): Show |
2 | a0001c0001t0001g0127a0005c0006t0001g0162 | 2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.566-130403_566-130 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557326 | |||||
| chrX:17557326
|
GAT | G | 5 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0099others(2): Show | 5 | HG01243.hp1 HG02293.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-130395_566-130 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557326 | |||||
| chrX:17557347
|
A | ATATATG | 1 | a0001c0001t0002g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.566-130394_566-130 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557347 | |||||
| chrX:17557349
|
C | G | 35 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(32): Show | 35 | HG00408.hp2 HG01071.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.566-130393C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17557349 | ||||||
| chrX:17557711
|
T | TG | 49 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(46): Show | 49 | HG00408.hp2 HG01071.hp2 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.566-130027dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557711 | |||||
| chrX:17557774
|
G | C | 12 | a0001c0001t0001g0127a0001c0001t0002g0004a0002c0002t0001g0014others(9): Show | 12 | HG00408.hp2 HG01928.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-129968G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17557774 | ||||||
| chrX:17558106
|
T | C | 12 | a0001c0001t0001g0127a0001c0001t0002g0004a0002c0002t0001g0014others(9): Show | 12 | HG00408.hp2 HG01928.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-129636T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17558106 | ||||||
| chrX:17558469
|
C | T | 25 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(22): Show | 25 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-129273C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17558469 | ||||||
| chrX:17558619
|
G | C | 56 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(53): Show | 56 | HG00408.hp2 HG01071.hp2 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.566-129123G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17558619 | ||||||
| chrX:17558730
|
A | G | 29 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(26): Show | 29 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.566-129012A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17558730 | ||||||
| chrX:17558780
|
T | C | 3 | a0002c0002t0001g0006a0002c0002t0001g0053a0002c0002t0001g0062 | 3 | NA18953.hp1 NA18966.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.566-128962T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17558780 | ||||||
| chrX:17559799
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.566-127943C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17559799 | ||||||
| chrX:17559800
|
C | A | 73 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(70): Show | 73 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.566-127942C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17559800 | ||||||
| chrX:17559845
|
T | C | 6 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-127897T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17559845 | ||||||
| chrX:17559926
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.566-127816C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17559926 | ||||||
| chrX:17559937
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.566-127805G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17559937 | ||||||
| chrX:17559967
|
A | AC | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.566-127772dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17559967 | |||||
| chrX:17560716
|
T | C | 6 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-127026T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17560716 | ||||||
| chrX:17561003
|
A | C | 2 | a0001c0001t0001g0026a0011c0013t0001g0039 | 2 | NA18747.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.566-126739A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561003 | ||||||
| chrX:17561189
|
C | T | 9 | a0001c0001t0002g0096a0001c0001t0002g0106a0001c0001t0002g0107others(6): Show | 9 | HG01071.hp2 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-126553C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561189 | ||||||
| chrX:17561381
|
A | G | 11 | a0001c0001t0001g0127a0001c0001t0002g0004a0002c0002t0001g0014others(8): Show | 11 | HG00408.hp2 HG01928.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.566-126361A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561381 | ||||||
| chrX:17561395
|
G | A | 1 | a0002c0002t0001g0082 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.566-126347G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561395 | ||||||
| chrX:17561408
|
A | AAG | 1 | a0001c0001t0001g0050 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.566-126331_566-126 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561408 | |||||
| chrX:17561450
|
G | C | 49 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(46): Show | 49 | HG00408.hp2 HG01071.hp2 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.566-126292G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561450 | ||||||
| chrX:17561468
|
G | T | 15 | a0001c0001t0002g0096a0001c0001t0002g0106a0001c0001t0002g0107others(12): Show | 15 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-126274G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561468 | ||||||
| chrX:17561557
|
T | TGC | 3 | a0002c0002t0001g0045a0002c0002t0001g0054a0002c0002t0001g0130 | 3 | HG00140.hp1 HG00738.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.566-126168_566-126 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561557 | |||||
| chrX:17561557
|
TGC | T | 5 | a0001c0001t0001g0041a0001c0001t0002g0043a0003c0004t0001g0149others(2): Show | 5 | HG01109.hp1 HG02451.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-126168_566-126 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561557 | |||||
| chrX:17561557
|
TGCGC | T | 4 | a0001c0001t0002g0004a0001c0001t0002g0107a0001c0001t0002g0110others(1): Show | 4 | HG02055.hp1 HG02809.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-126170_566-126 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561557 | |||||
| chrX:17561557
|
TGCGCGC | T | 5 | a0001c0001t0002g0106a0001c0001t0009g0125a0004c0005t0003g0136others(2): Show | 5 | HG01071.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-126172_566-126 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561557 | |||||
| chrX:17561564
|
GCGCGCGC others(5): Show |
G | 2 | a0001c0003t0002g0142a0006c0007t0002g0115 | 2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.566-126176_566-126 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561564 | |||||
| chrX:17561564
|
GCGCGCGC others(7): Show |
G | 4 | a0001c0003t0002g0019a0001c0003t0002g0128a0001c0003t0002g0155others(1): Show | 4 | HG01258.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-126176_566-126 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561564 | |||||
| chrX:17561564
|
GCGCGCGC others(9): Show |
G | 2 | a0001c0001t0001g0151a0002c0002t0006g0060 | 2 | HG00408.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.566-126176_566-126 others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561564 | |||||
| chrX:17561565
|
C | CGCT | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.566-126175_566-126 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561565 | |||||
| chrX:17561568
|
G | A | 1 | a0001c0001t0002g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.566-126174G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561568 | ||||||
| chrX:17561568
|
G | GCACA | 3 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0003t0002g0101 | 3 | HG02922.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.566-126173_566-126 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561568 | |||||
| chrX:17561568
|
G | GCACACAC others(1): Show |
2 | a0001c0001t0005g0111a0005c0006t0005g0159 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.566-126173_566-126 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561568 | |||||
| chrX:17561568
|
GCGCGCGC others(5): Show |
G | 1 | a0005c0006t0001g0162 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.566-126172_566-126 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561568 | |||||
| chrX:17561570
|
G | A | 11 | a0001c0001t0001g0127a0001c0001t0002g0085a0001c0001t0002g0096others(8): Show | 11 | HG01928.hp1 HG01952.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-126172G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561570 | ||||||
| chrX:17561570
|
G | GCA | 2 | a0001c0001t0017g0154a0004c0005t0010g0086 | 2 | HG01975.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.566-126171_566-126 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561570 | |||||
| chrX:17561570
|
G | GCACACA | 3 | a0004c0005t0003g0117a0006c0008t0008g0113a0007c0009t0002g0160 | 3 | HG02145.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.566-126171_566-126 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561570 | |||||
| chrX:17561570
|
G | GCACACAC others(1): Show |
2 | a0001c0001t0012g0044a0009c0011t0002g0147 | 2 | HG02257.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.566-126171_566-126 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561570 | |||||
| chrX:17561570
|
G | GCACACAC others(3): Show |
3 | a0001c0001t0002g0143a0001c0001t0002g0146a0005c0006t0001g0157 | 3 | HG01106.hp1 HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.566-126171_566-126 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561570 | |||||
| chrX:17561570
|
G | GCACACAC others(5): Show |
1 | a0001c0001t0002g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.566-126171_566-126 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561570 | |||||
| chrX:17561570
|
GCGCGCAC others(1): Show |
G | 1 | a0013c0016t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.566-126170_566-126 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561570 | |||||
| chrX:17561572
|
G | A | 28 | a0001c0001t0001g0127a0001c0001t0002g0085a0001c0001t0002g0096others(25): Show | 28 | HG01106.hp1 HG01243.hp1 HG01928.hp1 others(25): Show |
intron_variant | MODIFIER | c.566-126170G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561572 | ||||||
| chrX:17561572
|
G | GCA | 1 | a0002c0002t0001g0021 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.566-126169_566-126 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561572 | |||||
| chrX:17561572
|
G | GCACA | 4 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0002g0120others(1): Show | 4 | HG03041.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-126169_566-126 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561572 | |||||
| chrX:17561572
|
G | GCACACA | 2 | a0001c0001t0001g0068a0001c0001t0002g0116 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.566-126169_566-126 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561572 | |||||
| chrX:17561572
|
G | GCACACAC others(1): Show |
1 | a0001c0001t0009g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.566-126169_566-126 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561572 | |||||
| chrX:17561572
|
G | GCACACAC others(3): Show |
1 | a0008c0010t0003g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.566-126169_566-126 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561572 | |||||
| chrX:17561572
|
GCGCACA | G | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.566-126168_566-126 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561572 | |||||
| chrX:17561574
|
G | A | 46 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0090others(43): Show | 46 | HG00280.hp1 HG01071.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.566-126168G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561574 | ||||||
| chrX:17561574
|
G | GCA | 8 | a0001c0001t0001g0012a0001c0001t0001g0049a0001c0001t0001g0061others(5): Show | 8 | HG02071.hp1 HG02293.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-126123_566-126 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
G | GCACA | 4 | a0001c0001t0002g0002a0002c0002t0001g0023a0002c0002t0001g0051others(1): Show | 4 | HG02027.hp1 HG02293.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-126125_566-126 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
G | GCACACA | 8 | a0001c0001t0001g0070a0002c0002t0001g0011a0002c0002t0001g0014others(5): Show | 8 | HG00408.hp2 HG02698.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-126127_566-126 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
G | GCACACAC others(1): Show |
6 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0030others(3): Show | 6 | HG01975.hp2 HG02735.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-126129_566-126 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
G | GCACACAC others(3): Show |
5 | a0001c0001t0001g0026a0001c0001t0001g0029a0002c0002t0001g0016others(2): Show | 5 | HG02129.hp1 NA18747.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-126131_566-126 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
G | GCACACAC others(5): Show |
3 | a0001c0001t0002g0093a0001c0001t0002g0126a0002c0002t0001g0108 | 3 | HG01069.hp1 HG01071.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.566-126133_566-126 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
G | GCACACAC others(7): Show |
1 | a0002c0002t0001g0065 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.566-126135_566-126 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
G | GCACACAC others(11): Show |
1 | a0002c0002t0001g0148 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.566-126139_566-126 others(24): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
G | GCGCA | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.566-126167_566-126 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
G | GCGCACA | 1 | a0002c0002t0001g0075 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.566-126167_566-126 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
G | GCGCACAC others(1): Show |
3 | a0001c0001t0001g0145a0001c0001t0002g0121a0002c0002t0001g0091 | 3 | HG00639.hp2 HG02280.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.566-126167_566-126 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
G | GCGCACAC others(3): Show |
2 | a0002c0002t0001g0015a0002c0002t0001g0141 | 2 | HG02083.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.566-126167_566-126 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
G | GCGCACAC others(5): Show |
1 | a0002c0002t0001g0078 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.566-126167_566-126 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
G | GCGCACAC others(7): Show |
1 | a0002c0002t0001g0062 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.566-126167_566-126 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
G | GCGCGCAC others(1): Show |
1 | a0002c0002t0014g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.566-126167_566-126 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
G | GCGCGCAC others(3): Show |
2 | a0002c0002t0001g0053a0002c0002t0001g0084 | 2 | HG02015.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.566-126167_566-126 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
G | GCGCGCAC others(5): Show |
2 | a0002c0002t0001g0006a0002c0002t0001g0035 | 2 | HG04115.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.566-126167_566-126 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
G | GCGCGCAC others(7): Show |
1 | a0001c0001t0001g0048 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.566-126167_566-126 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
GCA | G | 15 | a0001c0001t0001g0036a0001c0001t0001g0050a0001c0001t0001g0056others(12): Show | 15 | HG00639.hp1 HG01074.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-126123_566-126 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
GCACA | G | 10 | a0001c0001t0001g0022a0001c0001t0001g0129a0001c0001t0001g0140others(7): Show | 10 | HG00642.hp1 HG00673.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-126125_566-126 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
GCACACA | G | 10 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0124others(7): Show | 10 | HG00609.hp1 HG01167.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-126127_566-126 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
GCACACAC others(1): Show |
G | 2 | a0001c0001t0001g0052a0001c0001t0013g0059 | 2 | NA18965.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.566-126129_566-126 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
GCACACAC others(3): Show |
G | 2 | a0001c0001t0015g0079a0002c0002t0016g0005 | 2 | HG00621.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.566-126131_566-126 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561574
|
GCACACAC others(9): Show |
G | 2 | a0001c0001t0007g0073a0001c0001t0007g0102 | 2 | NA18955.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.566-126137_566-126 others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | |||||
| chrX:17561576
|
A | G | 6 | a0001c0001t0001g0081a0002c0002t0001g0010a0002c0002t0001g0027others(3): Show | 6 | HG00140.hp1 HG01192.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-126166A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561576 | ||||||
| chrX:17561578
|
A | G | 6 | a0001c0001t0004g0163a0002c0002t0001g0018a0002c0002t0001g0027others(3): Show | 6 | HG00140.hp1 HG01074.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-126164A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561578 | ||||||
| chrX:17561580
|
A | G | 6 | a0001c0001t0001g0129a0001c0001t0001g0140a0001c0001t0004g0058others(3): Show | 6 | HG00642.hp1 HG01099.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-126162A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561580 | ||||||
| chrX:17561582
|
A | G | 1 | a0002c0015t0001g0046 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.566-126160A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561582 | ||||||
| chrX:17561584
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.566-126158A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561584 | ||||||
| chrX:17561801
|
A | C | 1 | a0002c0002t0001g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.566-125941A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561801 | ||||||
| chrX:17562070
|
T | C | 12 | a0001c0001t0001g0127a0001c0001t0002g0004a0002c0002t0001g0014others(9): Show | 12 | HG00408.hp2 HG01928.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-125672T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17562070 | ||||||
| chrX:17562530
|
T | C | 1 | a0004c0005t0010g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.566-125212T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17562530 | ||||||
| chrX:17562559
|
C | A | 1 | a0001c0001t0001g0050 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.566-125183C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17562559 | ||||||
| chrX:17562687
|
TAAAC | T | 1 | a0002c0002t0001g0008 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.566-125051_566-125 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17562687 | |||||
| chrX:17562880
|
A | AT | 157 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(154): Show | 157 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.566-124860dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17562880 | |||||
| chrX:17562914
|
G | A | 6 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-124828G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17562914 | ||||||
| chrX:17563124
|
A | G | 12 | a0001c0001t0001g0127a0001c0001t0002g0004a0002c0002t0001g0014others(9): Show | 12 | HG00408.hp2 HG01928.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-124618A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17563124 | ||||||
| chrX:17563143
|
C | T | 1 | a0002c0002t0001g0015 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.566-124599C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17563143 | ||||||
| chrX:17563682
|
C | T | 73 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(70): Show | 73 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.566-124060C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17563682 | ||||||
| chrX:17563683
|
G | C | 15 | a0001c0001t0002g0096a0001c0001t0002g0106a0001c0001t0002g0107others(12): Show | 15 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-124059G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17563683 | ||||||
| chrX:17563782
|
C | T | 10 | a0001c0001t0001g0127a0001c0001t0002g0004a0002c0002t0001g0014others(7): Show | 10 | HG00408.hp2 HG01952.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-123960C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17563782 | ||||||
| chrX:17564331
|
A | G | 1 | a0002c0002t0001g0077 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.566-123411A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17564331 | ||||||
| chrX:17564577
|
A | G | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0127others(18): Show | 21 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.566-123165A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17564577 | ||||||
| chrX:17564622
|
C | G | 1 | a0002c0002t0001g0156 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.566-123120C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17564622 | ||||||
| chrX:17564969
|
A | AT | 5 | a0001c0001t0001g0127a0002c0002t0001g0072a0002c0002t0001g0080others(2): Show | 5 | HG01952.hp1 HG02922.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-122764dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17564969 | |||||
| chrX:17564975
|
TTTTA | T | 5 | a0001c0003t0002g0019a0001c0003t0002g0128a0001c0003t0002g0142others(2): Show | 5 | HG01258.hp1 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-122759_566-122 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17564975 | |||||
| chrX:17564976
|
TTTA | T | 13 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0002g0096others(10): Show | 13 | HG01106.hp1 HG02055.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.566-122763_566-122 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17564976 | |||||
| chrX:17564977
|
TTA | T | 5 | a0001c0001t0002g0043a0001c0001t0009g0125a0004c0005t0003g0136others(2): Show | 5 | HG01071.hp2 HG01109.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-122763_566-122 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17564977 | |||||
| chrX:17564978
|
TA | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-122763delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17564978 | ||||||
| chrX:17564979
|
A | T | 9 | a0001c0001t0001g0127a0001c0001t0002g0004a0002c0002t0001g0072others(6): Show | 9 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-122763A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17564979 | ||||||
| chrX:17564983
|
A | T | 34 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(31): Show | 34 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.566-122759A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17564983 | ||||||
| chrX:17565051
|
CTGACTTT others(1): Show |
C | 9 | a0001c0001t0001g0127a0001c0001t0002g0004a0002c0002t0001g0072others(6): Show | 9 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-122684_566-122 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17565051 | |||||
| chrX:17565139
|
G | A | 1 | a0002c0002t0001g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.566-122603G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17565139 | ||||||
| chrX:17565320
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0144 | 2 | NA18943.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.566-122422C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17565320 | ||||||
| chrX:17565399
|
A | C | 1 | a0002c0002t0001g0074 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.566-122343A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17565399 | ||||||
| chrX:17565983
|
C | CT | 6 | a0001c0001t0001g0036a0001c0001t0002g0043a0001c0001t0002g0099others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-121743dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17565983 | |||||
| chrX:17565983
|
CT | C | 19 | a0001c0001t0001g0012a0001c0001t0001g0049a0001c0001t0001g0127others(16): Show | 19 | HG01952.hp1 HG02071.hp1 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.566-121743delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17565983 | |||||
| chrX:17566068
|
A | C | 9 | a0001c0001t0001g0127a0001c0001t0002g0004a0002c0002t0001g0072others(6): Show | 9 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-121674A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566068 | ||||||
| chrX:17566241
|
C | T | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.566-121501C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566241 | ||||||
| chrX:17566258
|
C | T | 9 | a0001c0001t0001g0127a0001c0001t0002g0004a0002c0002t0001g0072others(6): Show | 9 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-121484C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566258 | ||||||
| chrX:17566286
|
G | C | 9 | a0001c0001t0001g0127a0001c0001t0002g0004a0002c0002t0001g0072others(6): Show | 9 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-121456G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566286 | ||||||
| chrX:17566459
|
G | A | 5 | a0002c0002t0001g0072a0002c0002t0001g0080a0003c0004t0001g0132others(2): Show | 5 | HG01952.hp1 HG03017.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-121283G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566459 | ||||||
| chrX:17566537
|
C | T | 1 | a0002c0002t0001g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.566-121205C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566537 | ||||||
| chrX:17566544
|
A | G | 9 | a0001c0001t0001g0127a0001c0001t0002g0004a0002c0002t0001g0072others(6): Show | 9 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-121198A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566544 | ||||||
| chrX:17566600
|
G | A | 81 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.566-121142G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566600 | ||||||
| chrX:17566612
|
G | A | 117 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(114): Show | 117 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.566-121130G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566612 | ||||||
| chrX:17566693
|
T | G | 115 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(112): Show | 115 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.566-121049T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566693 | ||||||
| chrX:17566697
|
T | G | 81 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.566-121045T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566697 | ||||||
| chrX:17566754
|
T | C | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.566-120988T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566754 | ||||||
| chrX:17566755
|
G | T | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.566-120987G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566755 | ||||||
| chrX:17567020
|
G | A | 10 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0050others(7): Show | 10 | HG02040.hp1 NA18960.hp1 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-120722G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17567020 | ||||||
| chrX:17567782
|
G | A | 6 | a0001c0003t0002g0019a0001c0003t0002g0128a0001c0003t0002g0142others(3): Show | 6 | HG01258.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-119960G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17567782 | ||||||
| chrX:17567814
|
G | A | 31 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(28): Show | 31 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.566-119928G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17567814 | ||||||
| chrX:17567874
|
A | G | 3 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0009g0122 | 3 | HG02615.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.566-119868A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17567874 | ||||||
| chrX:17568227
|
C | A | 115 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(112): Show | 115 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.566-119515C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17568227 | ||||||
| chrX:17568520
|
C | CT | 2 | a0001c0001t0002g0121a0008c0010t0003g0158 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.566-119208dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17568520 | |||||
| chrX:17568520
|
C | CTT | 10 | a0001c0001t0001g0127a0002c0002t0001g0014a0002c0002t0001g0072others(7): Show | 10 | HG00408.hp2 HG01952.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-119209_566-119 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17568520 | |||||
| chrX:17568647
|
G | GTTA | 111 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0029others(108): Show | 111 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.566-119060_566-119 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17568647 | |||||
| chrX:17568647
|
G | GTTATTA | 24 | a0001c0001t0001g0026a0001c0001t0001g0048a0001c0001t0001g0124others(21): Show | 24 | HG01943.hp1 HG01952.hp1 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.566-119063_566-119 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17568647 | |||||
| chrX:17568647
|
G | GTTATTAT others(2): Show |
2 | a0003c0004t0001g0149a0010c0012t0001g0150 | 2 | NA18948.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.566-119066_566-119 others(15): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17568647 | |||||
| chrX:17568647
|
G | GTTGTTA | 1 | a0001c0001t0001g0057 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.566-119093_566-119 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17568647 | |||||
| chrX:17568647
|
G | GTTGTTAT others(5): Show |
1 | a0001c0001t0001g0022 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.566-119093_566-119 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17568647 | |||||
| chrX:17568647
|
GTTA | G | 6 | a0001c0001t0001g0068a0001c0001t0001g0081a0001c0001t0002g0043others(3): Show | 6 | HG01106.hp1 HG01109.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-119060_566-119 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17568647 | |||||
| chrX:17568647
|
GTTATTA | G | 2 | a0001c0001t0001g0041a0004c0005t0003g0117 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.566-119063_566-119 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17568647 | |||||
| chrX:17568647
|
GTTATTAT others(5): Show |
G | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-119069_566-119 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17568647 | |||||
| chrX:17568973
|
T | C | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.566-118769T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17568973 | ||||||
| chrX:17569113
|
C | T | 1 | a0004c0005t0010g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.566-118629C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569113 | ||||||
| chrX:17569178
|
C | A | 6 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-118564C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569178 | ||||||
| chrX:17569192
|
T | G | 13 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0099others(10): Show | 13 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.566-118550T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569192 | ||||||
| chrX:17569351
|
C | T | 46 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(43): Show | 46 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.566-118391C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569351 | ||||||
| chrX:17569359
|
TAA | T | 46 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(43): Show | 46 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.566-118380_566-118 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17569359 | |||||
| chrX:17569386
|
T | A | 13 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0099others(10): Show | 13 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.566-118356T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569386 | ||||||
| chrX:17569521
|
T | G | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.566-118221T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569521 | ||||||
| chrX:17569638
|
A | C | 13 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0099others(10): Show | 13 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.566-118104A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569638 | ||||||
| chrX:17569639
|
G | A | 13 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0099others(10): Show | 13 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.566-118103G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569639 | ||||||
| chrX:17569652
|
G | T | 21 | a0001c0001t0001g0127a0001c0001t0001g0137a0001c0001t0002g0002others(18): Show | 21 | HG01243.hp1 HG01952.hp1 HG01975.hp1 others(18): Show |
intron_variant | MODIFIER | c.566-118090G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569652 | ||||||
| chrX:17569672
|
A | C | 1 | a0004c0005t0003g0136 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.566-118070A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569672 | ||||||
| chrX:17569730
|
T | C | 13 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0099others(10): Show | 13 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.566-118012T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569730 | ||||||
| chrX:17569939
|
T | G | 9 | a0001c0001t0001g0127a0002c0002t0001g0014a0002c0002t0001g0072others(6): Show | 9 | HG00408.hp2 HG01952.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-117803T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569939 | ||||||
| chrX:17570148
|
G | A | 1 | a0001c0003t0002g0142 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.566-117594G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17570148 | ||||||
| chrX:17570185
|
G | GT | 1 | a0001c0001t0002g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.566-117550dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17570185 | |||||
| chrX:17570481
|
G | T | 8 | a0001c0001t0001g0127a0002c0002t0001g0072a0002c0002t0001g0080others(5): Show | 8 | HG01952.hp1 HG02922.hp1 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-117261G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17570481 | ||||||
| chrX:17570718
|
C | T | 29 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(26): Show | 29 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.566-117024C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17570718 | ||||||
| chrX:17570864
|
G | A | 15 | a0001c0001t0002g0096a0001c0001t0002g0106a0001c0001t0002g0107others(12): Show | 15 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-116878G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17570864 | ||||||
| chrX:17570963
|
G | A | 1 | a0002c0002t0001g0152 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.566-116779G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17570963 | ||||||
| chrX:17571052
|
C | T | 116 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(113): Show | 116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.566-116690C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571052 | ||||||
| chrX:17571109
|
G | A | 115 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(112): Show | 115 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.566-116633G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571109 | ||||||
| chrX:17571255
|
T | G | 1 | a0002c0002t0001g0017 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.566-116487T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571255 | ||||||
| chrX:17571303
|
T | C | 116 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(113): Show | 116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.566-116439T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571303 | ||||||
| chrX:17571397
|
A | G | 125 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(122): Show | 125 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.566-116345A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571397 | ||||||
| chrX:17571539
|
A | G | 116 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(113): Show | 116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.566-116203A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571539 | ||||||
| chrX:17571572
|
T | C | 9 | a0001c0001t0001g0127a0002c0002t0001g0014a0002c0002t0001g0072others(6): Show | 9 | HG00408.hp2 HG01952.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-116170T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571572 | ||||||
| chrX:17571609
|
A | G | 1 | a0002c0002t0011g0020 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.566-116133A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571609 | ||||||
| chrX:17571756
|
G | A | 1 | a0002c0002t0001g0014 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.566-115986G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571756 | ||||||
| chrX:17571778
|
A | T | 116 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(113): Show | 116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.566-115964A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571778 | ||||||
| chrX:17572135
|
G | A | 47 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(44): Show | 47 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.566-115607G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17572135 | ||||||
| chrX:17572181
|
T | C | 1 | a0001c0001t0006g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.566-115561T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17572181 | ||||||
| chrX:17572446
|
T | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.566-115296T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17572446 | ||||||
| chrX:17572491
|
C | CCTT | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-115251_566-115 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17572491 | ||||||
| chrX:17572491
|
C | CT | 56 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0029others(53): Show | 56 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.566-115229dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | |||||
| chrX:17572491
|
C | CTT | 24 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0144others(21): Show | 24 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.566-115230_566-115 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | |||||
| chrX:17572491
|
C | CTTT | 3 | a0001c0001t0002g0043a0001c0001t0002g0106a0005c0006t0001g0157 | 3 | HG01106.hp1 HG01109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.566-115231_566-115 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | |||||
| chrX:17572491
|
C | CTTTT | 6 | a0001c0001t0001g0137a0001c0001t0002g0085a0001c0001t0005g0103others(3): Show | 6 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-115232_566-115 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | |||||
| chrX:17572491
|
C | CTTTTT | 1 | a0001c0003t0002g0101 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.566-115233_566-115 others(11): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | |||||
| chrX:17572491
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0002g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.566-115242_566-115 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | |||||
| chrX:17572491
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0002g0099a0001c0001t0002g0146 | 2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.566-115243_566-115 others(21): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | |||||
| chrX:17572491
|
C | CTTTTTTT others(9): Show |
2 | a0001c0001t0002g0116a0001c0001t0017g0154 | 2 | HG01975.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.566-115244_566-115 others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | |||||
| chrX:17572491
|
C | CTTTTTTT others(10): Show |
3 | a0001c0001t0002g0002a0001c0001t0009g0122a0008c0010t0003g0158 | 3 | HG02293.hp2 HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.566-115245_566-115 others(23): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | |||||
| chrX:17572491
|
C | CTTTTTTT others(11): Show |
2 | a0001c0001t0012g0044a0004c0005t0010g0086 | 2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.566-115246_566-115 others(24): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | |||||
| chrX:17572491
|
C | CTTTTTTT others(12): Show |
1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.566-115247_566-115 others(25): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | |||||
| chrX:17572491
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0002g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.566-115250_566-115 others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | |||||
| chrX:17572491
|
CT | C | 1 | a0001c0001t0001g0009 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.566-115229delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | |||||
| chrX:17572491
|
CTTTTTTT others(2): Show |
C | 9 | a0001c0001t0001g0127a0001c0001t0002g0004a0002c0002t0001g0072others(6): Show | 9 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-115237_566-115 others(15): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | |||||
| chrX:17572576
|
C | A | 15 | a0001c0001t0002g0096a0001c0001t0002g0106a0001c0001t0002g0107others(12): Show | 15 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-115166C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17572576 | ||||||
| chrX:17572719
|
C | T | 1 | a0002c0002t0001g0078 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.566-115023C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17572719 | ||||||
| chrX:17572927
|
G | T | 22 | a0001c0001t0001g0127a0001c0001t0001g0137a0001c0001t0002g0002others(19): Show | 22 | HG01243.hp1 HG01952.hp1 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.566-114815G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17572927 | ||||||
| chrX:17572935
|
T | A | 9 | a0001c0001t0001g0127a0001c0001t0002g0004a0002c0002t0001g0072others(6): Show | 9 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-114807T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17572935 | ||||||
| chrX:17572958
|
G | T | 116 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(113): Show | 116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.566-114784G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17572958 | ||||||
| chrX:17573188
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0002g0002 | 2 | HG02293.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.566-114554G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17573188 | ||||||
| chrX:17573518
|
T | G | 6 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-114224T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17573518 | ||||||
| chrX:17573525
|
C | T | 6 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-114217C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17573525 | ||||||
| chrX:17573669
|
C | T | 2 | a0002c0002t0001g0018a0002c0002t0001g0123 | 2 | HG00639.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.566-114073C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17573669 | ||||||
| chrX:17573725
|
G | A | 2 | a0002c0002t0001g0033a0003c0004t0001g0013 | 2 | HG01192.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.566-114017G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17573725 | ||||||
| chrX:17574503
|
G | A | 79 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(76): Show | 79 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.566-113239G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17574503 | ||||||
| chrX:17574591
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.566-113151A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17574591 | ||||||
| chrX:17574639
|
G | A | 2 | a0002c0002t0001g0087a0002c0002t0001g0088 | 2 | NA18945.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.566-113103G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17574639 | ||||||
| chrX:17574643
|
C | T | 1 | a0001c0001t0001g0009 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.566-113099C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17574643 | ||||||
| chrX:17574718
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.566-113024C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17574718 | ||||||
| chrX:17574918
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.566-112824G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17574918 | ||||||
| chrX:17575050
|
C | CT | 1 | a0001c0001t0001g0049 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.566-112691dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17575050 | |||||
| chrX:17575124
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.566-112618G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17575124 | ||||||
| chrX:17575219
|
C | T | 115 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(112): Show | 115 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.566-112523C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17575219 | ||||||
| chrX:17575351
|
C | CCATCACC others(13): Show |
1 | a0006c0008t0008g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.566-112347_566-112 others(26): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17575351 | |||||
| chrX:17575351
|
CCATCACC others(13): Show |
C | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.566-112347_566-112 others(26): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17575351 | |||||
| chrX:17575360
|
G | GT | 1 | a0001c0001t0001g0049 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.566-112377dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17575360 | |||||
| chrX:17575457
|
C | T | 80 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(77): Show | 80 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.566-112285C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17575457 | ||||||
| chrX:17575582
|
A | G | 1 | a0001c0003t0002g0155 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.566-112160A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17575582 | ||||||
| chrX:17575783
|
A | G | 127 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(124): Show | 127 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.566-111959A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17575783 | ||||||
| chrX:17575937
|
A | G | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.566-111805A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17575937 | ||||||
| chrX:17576160
|
C | T | 104 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(101): Show | 104 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.566-111582C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17576160 | ||||||
| chrX:17576347
|
T | C | 10 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(7): Show | 10 | HG01106.hp1 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-111395T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17576347 | ||||||
| chrX:17576691
|
G | A | 1 | a0002c0002t0001g0075 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.566-111051G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17576691 | ||||||
| chrX:17577107
|
C | T | 1 | a0002c0002t0001g0015 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.566-110635C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17577107 | ||||||
| chrX:17577201
|
G | A | 115 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(112): Show | 115 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.566-110541G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17577201 | ||||||
| chrX:17577826
|
T | G | 9 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0003t0002g0019others(6): Show | 9 | HG01258.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-109916T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17577826 | ||||||
| chrX:17578097
|
A | G | 12 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0099others(9): Show | 12 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-109645A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17578097 | ||||||
| chrX:17578156
|
G | C | 12 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0099others(9): Show | 12 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-109586G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17578156 | ||||||
| chrX:17578417
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.566-109325C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17578417 | ||||||
| chrX:17578590
|
C | T | 1 | a0002c0002t0001g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.566-109152C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17578590 | ||||||
| chrX:17578644
|
A | C | 1 | a0001c0001t0002g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.566-109098A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17578644 | ||||||
| chrX:17578848
|
G | T | 51 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(48): Show | 51 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.566-108894G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17578848 | ||||||
| chrX:17579152
|
TATC | T | 1 | a0002c0002t0001g0024 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.566-108587_566-108 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17579152 | |||||
| chrX:17579154
|
T | A | 13 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0099others(10): Show | 13 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.566-108588T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17579154 | ||||||
| chrX:17579165
|
G | A | 2 | a0002c0002t0001g0138a0002c0002t0001g0139 | 2 | HG00673.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.566-108577G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17579165 | ||||||
| chrX:17579469
|
T | C | 13 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0099others(10): Show | 13 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.566-108273T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17579469 | ||||||
| chrX:17579688
|
G | A | 50 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(47): Show | 50 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.566-108054G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17579688 | ||||||
| chrX:17579760
|
C | T | 1 | a0001c0001t0009g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.566-107982C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17579760 | ||||||
| chrX:17579876
|
A | G | 12 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0099others(9): Show | 12 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-107866A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17579876 | ||||||
| chrX:17580181
|
GA | G | 24 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(21): Show | 24 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.566-107549delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17580181 | |||||
| chrX:17580181
|
GAA | G | 12 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0099others(9): Show | 12 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-107550_566-107 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17580181 | |||||
| chrX:17580810
|
C | T | 8 | a0001c0001t0001g0127a0002c0002t0001g0072a0002c0002t0001g0080others(5): Show | 8 | HG01952.hp1 HG02922.hp1 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-106932C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17580810 | ||||||
| chrX:17581021
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.566-106721A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17581021 | ||||||
| chrX:17581054
|
G | A | 24 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0094others(21): Show | 24 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.566-106688G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17581054 | ||||||
| chrX:17581402
|
G | T | 8 | a0001c0001t0001g0127a0002c0002t0001g0072a0002c0002t0001g0080others(5): Show | 8 | HG01952.hp1 HG02922.hp1 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-106340G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17581402 | ||||||
| chrX:17581796
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-105946C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17581796 | ||||||
| chrX:17582740
|
C | T | 48 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0048others(45): Show | 48 | HG00280.hp1 HG00639.hp2 HG01261.hp1 others(45): Show |
intron_variant | MODIFIER | c.566-105002C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17582740 | ||||||
| chrX:17583407
|
C | T | 6 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0002g0043others(3): Show | 6 | HG01106.hp1 HG01109.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-104335C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17583407 | ||||||
| chrX:17583471
|
AG | A | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.566-104268delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17583471 | |||||
| chrX:17583535
|
G | C | 9 | a0001c0001t0001g0127a0001c0001t0002g0004a0002c0002t0001g0072others(6): Show | 9 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-104207G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17583535 | ||||||
| chrX:17583887
|
C | A | 1 | a0001c0001t0004g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.566-103855C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17583887 | ||||||
| chrX:17584195
|
T | C | 6 | a0001c0003t0002g0019a0001c0003t0002g0128a0001c0003t0002g0142others(3): Show | 6 | HG01258.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-103547T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584195 | ||||||
| chrX:17584334
|
A | C | 116 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(113): Show | 116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.566-103408A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584334 | ||||||
| chrX:17584340
|
C | T | 4 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0009g0122others(1): Show | 4 | HG02615.hp2 HG02723.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-103402C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584340 | ||||||
| chrX:17584408
|
T | C | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.566-103334T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584408 | ||||||
| chrX:17584434
|
A | G | 1 | a0002c0002t0001g0021 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.566-103308A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584434 | ||||||
| chrX:17584461
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.566-103281C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584461 | ||||||
| chrX:17584734
|
T | C | 16 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0002g0106others(13): Show | 16 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.566-103008T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584734 | ||||||
| chrX:17584847
|
T | C | 128 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(125): Show | 128 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.566-102895T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584847 | ||||||
| chrX:17584913
|
C | G | 1 | a0001c0003t0002g0019 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.566-102829C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584913 | ||||||
| chrX:17584997
|
C | T | 106 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0029others(103): Show | 106 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.566-102745C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584997 | ||||||
| chrX:17585418
|
G | A | 12 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0099others(9): Show | 12 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-102324G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17585418 | ||||||
| chrX:17585458
|
A | AT | 1 | a0001c0001t0001g0050 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.566-102280dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17585458 | |||||
| chrX:17585555
|
A | G | 12 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0099others(9): Show | 12 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-102187A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17585555 | ||||||
| chrX:17585658
|
A | G | 28 | a0001c0001t0001g0127a0001c0001t0001g0137a0001c0001t0002g0002others(25): Show | 28 | HG00408.hp2 HG01071.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.566-102084A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17585658 | ||||||
| chrX:17585738
|
G | GTAA | 9 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0049others(6): Show | 9 | HG00673.hp1 HG01109.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-101976_566-101 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17585738 | |||||
| chrX:17585738
|
G | GTAATAAT others(2): Show |
5 | a0002c0002t0001g0014a0002c0002t0001g0072a0002c0002t0001g0075others(2): Show | 5 | HG00408.hp2 HG01952.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-101982_566-101 others(15): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17585738 | |||||
| chrX:17585738
|
G | GTAATAAT others(5): Show |
4 | a0003c0004t0001g0149a0005c0006t0001g0162a0005c0006t0008g0161others(1): Show | 4 | HG02922.hp1 HG03471.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-101985_566-101 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17585738 | |||||
| chrX:17585738
|
G | GTAATAAT others(8): Show |
1 | a0001c0001t0001g0127 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.566-101988_566-101 others(21): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17585738 | |||||
| chrX:17585738
|
GTAA | G | 11 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0116others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-101976_566-101 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17585738 | |||||
| chrX:17585753
|
A | T | 3 | a0001c0001t0012g0044a0004c0005t0010g0086a0009c0011t0002g0147 | 3 | HG02257.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.566-101989A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17585753 | ||||||
| chrX:17585836
|
G | GT | 23 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0095others(20): Show | 23 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.566-101898dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17585836 | |||||
| chrX:17585837
|
T | G | 22 | a0001c0001t0001g0127a0001c0001t0001g0137a0001c0001t0002g0002others(19): Show | 22 | HG00408.hp2 HG01243.hp1 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.566-101905T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17585837 | ||||||
| chrX:17585977
|
G | A | 1 | a0002c0002t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.566-101765G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17585977 | ||||||
| chrX:17586107
|
C | T | 5 | a0001c0001t0001g0041a0001c0001t0002g0121a0004c0005t0003g0117others(2): Show | 5 | HG01106.hp1 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-101635C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17586107 | ||||||
| chrX:17586676
|
C | T | 12 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0099others(9): Show | 12 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-101066C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17586676 | ||||||
| chrX:17587181
|
C | CA | 1 | a0001c0001t0001g0050 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.566-100556dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17587181 | |||||
| chrX:17587208
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.566-100534G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17587208 | ||||||
| chrX:17587419
|
T | C | 4 | a0001c0001t0009g0125a0004c0005t0003g0100a0004c0005t0003g0136others(1): Show | 4 | HG01071.hp2 HG02055.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-100323T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17587419 | ||||||
| chrX:17587688
|
G | A | 6 | a0001c0003t0002g0019a0001c0003t0002g0128a0001c0003t0002g0142others(3): Show | 6 | HG01258.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-100054G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17587688 | ||||||
| chrX:17588256
|
A | G | 101 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0041others(98): Show | 101 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.566-99486A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17588256 | ||||||
| chrX:17588590
|
G | A | 1 | a0012c0014t0003g0092 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.566-99152G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17588590 | ||||||
| chrX:17588591
|
AT | A | 89 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0048others(86): Show | 89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.566-99139delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17588591 | |||||
| chrX:17588611
|
T | TC | 1 | a0002c0002t0001g0011 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.566-99131_566-9913 others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17588611 | ||||||
| chrX:17588703
|
C | G | 75 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0048others(72): Show | 75 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.566-99039C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17588703 | ||||||
| chrX:17588970
|
C | T | 10 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0095others(7): Show | 10 | HG01106.hp1 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-98772C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17588970 | ||||||
| chrX:17589023
|
C | T | 10 | a0001c0001t0009g0125a0001c0003t0002g0019a0001c0003t0002g0128others(7): Show | 10 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-98719C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17589023 | ||||||
| chrX:17589156
|
TATTTTTT others(1): Show |
T | 4 | a0001c0001t0001g0068a0001c0001t0002g0096a0001c0001t0006g0112others(1): Show | 4 | HG02486.hp1 HG02723.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-98577_566-9857 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17589156 | |||||
| chrX:17589201
|
C | T | 89 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0048others(86): Show | 89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.566-98541C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17589201 | ||||||
| chrX:17589319
|
T | C | 109 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0041others(106): Show | 109 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.566-98423T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17589319 | ||||||
| chrX:17589571
|
C | A | 89 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0048others(86): Show | 89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.566-98171C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17589571 | ||||||
| chrX:17589650
|
A | AGTGAGTA others(213): Show |
1 | a0003c0004t0001g0132 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.566-98077_566-9807 others(224): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17589650 | |||||
| chrX:17589650
|
A | AGTGAGTA others(212): Show |
1 | a0005c0006t0001g0162 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.566-98077_566-9807 others(223): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17589650 | |||||
| chrX:17589650
|
A | AGTGAGTA others(213): Show |
5 | a0001c0001t0001g0127a0002c0002t0001g0072a0002c0002t0001g0080others(2): Show | 5 | HG03017.hp1 HG03453.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-98077_566-9807 others(224): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17589650 | |||||
| chrX:17589650
|
A | AGTGAGTA others(214): Show |
2 | a0002c0002t0001g0075a0010c0012t0001g0150 | 2 | HG04228.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.566-98077_566-9807 others(225): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17589650 | |||||
| chrX:17589677
|
T | C | 2 | a0001c0001t0004g0069a0001c0001t0004g0163 | 2 | HG01261.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.566-98065T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17589677 | ||||||
| chrX:17589934
|
G | C | 6 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-97808G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17589934 | ||||||
| chrX:17589958
|
T | C | 1 | a0001c0003t0002g0101 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.566-97784T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17589958 | ||||||
| chrX:17589988
|
G | A | 1 | a0003c0004t0001g0013 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.566-97754G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17589988 | ||||||
| chrX:17590235
|
C | T | 9 | a0001c0001t0001g0127a0002c0002t0001g0072a0002c0002t0001g0075others(6): Show | 9 | HG01952.hp1 HG02922.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-97507C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17590235 | ||||||
| chrX:17590814
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.566-96928C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17590814 | ||||||
| chrX:17590818
|
C | A | 5 | a0002c0002t0001g0015a0002c0002t0001g0023a0002c0002t0001g0087others(2): Show | 5 | HG02027.hp1 HG02083.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-96924C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17590818 | ||||||
| chrX:17590837
|
A | G | 1 | a0002c0002t0001g0064 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.566-96905A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17590837 | ||||||
| chrX:17590855
|
A | G | 32 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0095others(29): Show | 32 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.566-96887A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17590855 | ||||||
| chrX:17591075
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.566-96667C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17591075 | ||||||
| chrX:17591284
|
T | G | 7 | a0002c0002t0001g0015a0002c0002t0001g0023a0002c0002t0001g0024others(4): Show | 7 | HG02027.hp1 HG02083.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-96458T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17591284 | ||||||
| chrX:17591303
|
C | T | 7 | a0002c0002t0001g0015a0002c0002t0001g0023a0002c0002t0001g0024others(4): Show | 7 | HG02027.hp1 HG02083.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-96439C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17591303 | ||||||
| chrX:17591659
|
C | T | 1 | a0002c0002t0001g0084 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.566-96083C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17591659 | ||||||
| chrX:17591677
|
A | T | 20 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0095others(17): Show | 20 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.566-96065A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17591677 | ||||||
| chrX:17591815
|
G | A | 4 | a0001c0001t0009g0125a0004c0005t0003g0100a0004c0005t0003g0136others(1): Show | 4 | HG01071.hp2 HG02055.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-95927G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17591815 | ||||||
| chrX:17592010
|
A | ATG | 14 | a0001c0001t0001g0041a0001c0001t0001g0145a0001c0001t0002g0121others(11): Show | 14 | HG00280.hp1 HG00639.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.566-95706_566-9570 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17592010 | |||||
| chrX:17592010
|
A | ATGTG | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-95708_566-9570 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17592010 | |||||
| chrX:17592010
|
ATG | A | 12 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0099others(9): Show | 12 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-95706_566-9570 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17592010 | |||||
| chrX:17592010
|
ATGTG | A | 11 | a0001c0001t0002g0043a0001c0001t0002g0085a0001c0001t0005g0103others(8): Show | 11 | HG01071.hp2 HG01109.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.566-95708_566-9570 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17592010 | |||||
| chrX:17592023
|
T | TC | 1 | a0002c0002t0001g0037 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.566-95719_566-9571 others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17592023 | ||||||
| chrX:17592119
|
T | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.566-95623T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17592119 | ||||||
| chrX:17592176
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-95566C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17592176 | ||||||
| chrX:17592178
|
G | A | 41 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0095others(38): Show | 41 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.566-95564G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17592178 | ||||||
| chrX:17592411
|
C | T | 32 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0095others(29): Show | 32 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.566-95331C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17592411 | ||||||
| chrX:17592979
|
G | A | 109 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0041others(106): Show | 109 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.566-94763G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17592979 | ||||||
| chrX:17593263
|
C | G | 89 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0048others(86): Show | 89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.566-94479C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17593263 | ||||||
| chrX:17593556
|
T | C | 89 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0048others(86): Show | 89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.566-94186T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17593556 | ||||||
| chrX:17593746
|
C | CATGTCT | 1 | a0004c0005t0003g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.566-93983_566-9397 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17593746 | |||||
| chrX:17594076
|
T | C | 1 | a0002c0002t0001g0030 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.566-93666T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17594076 | ||||||
| chrX:17594183
|
G | A | 41 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0095others(38): Show | 41 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.566-93559G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17594183 | ||||||
| chrX:17594376
|
G | A | 80 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0048others(77): Show | 80 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.566-93366G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17594376 | ||||||
| chrX:17594732
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0056 | 2 | NA18988.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.566-93010C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17594732 | ||||||
| chrX:17595340
|
C | T | 118 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0041others(115): Show | 118 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.566-92402C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17595340 | ||||||
| chrX:17595354
|
G | A | 1 | a0001c0001t0015g0079 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.566-92388G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17595354 | ||||||
| chrX:17595560
|
G | T | 2 | a0001c0001t0007g0073a0001c0001t0007g0102 | 2 | NA18955.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.566-92182G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17595560 | ||||||
| chrX:17596041
|
CA | C | 89 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0048others(86): Show | 89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.566-91690delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17596041 | |||||
| chrX:17596196
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.566-91546A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17596196 | ||||||
| chrX:17596348
|
G | C | 6 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-91394G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17596348 | ||||||
| chrX:17596399
|
C | T | 80 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0048others(77): Show | 80 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.566-91343C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17596399 | ||||||
| chrX:17596697
|
A | G | 6 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-91045A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17596697 | ||||||
| chrX:17597116
|
G | GT | 23 | a0001c0001t0001g0029a0001c0001t0001g0090a0001c0001t0001g0127others(20): Show | 23 | HG00639.hp2 HG01952.hp1 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.566-90605dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17597116 | |||||
| chrX:17597116
|
G | GTT | 2 | a0002c0002t0001g0021a0002c0002t0001g0075 | 2 | HG00280.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.566-90606_566-9060 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17597116 | |||||
| chrX:17597116
|
G | GTTT | 1 | a0002c0002t0001g0024 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.566-90607_566-9060 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17597116 | |||||
| chrX:17597116
|
GT | G | 2 | a0002c0002t0001g0105a0005c0006t0005g0159 | 2 | HG02622.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.566-90605delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17597116 | |||||
| chrX:17597116
|
GTT | G | 5 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(2): Show | 5 | HG02630.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-90606_566-9060 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17597116 | |||||
| chrX:17597116
|
GTTTTT | G | 32 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0095others(29): Show | 32 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.566-90609_566-9060 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17597116 | |||||
| chrX:17597215
|
G | A | 32 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0095others(29): Show | 32 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.566-90527G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17597215 | ||||||
| chrX:17597245
|
A | G | 32 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0095others(29): Show | 32 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.566-90497A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17597245 | ||||||
| chrX:17597247
|
A | G | 32 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0095others(29): Show | 32 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.566-90495A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17597247 | ||||||
| chrX:17597372
|
A | G | 47 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0095others(44): Show | 47 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.566-90370A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17597372 | ||||||
| chrX:17597426
|
T | TTC | 3 | a0003c0004t0001g0132a0003c0004t0001g0149a0010c0012t0001g0150 | 3 | HG01952.hp1 NA18948.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.566-90312_566-9031 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17597426 | |||||
| chrX:17597430
|
C | CT | 11 | a0001c0001t0002g0085a0001c0001t0002g0106a0001c0001t0002g0107others(8): Show | 11 | HG02258.hp1 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-90296dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17597430 | |||||
| chrX:17597430
|
C | CTT | 6 | a0001c0001t0001g0127a0002c0002t0001g0072a0002c0002t0001g0075others(3): Show | 6 | HG02922.hp1 HG03017.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-90297_566-9029 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17597430 | |||||
| chrX:17597430
|
CT | C | 5 | a0001c0001t0004g0069a0002c0002t0001g0016a0002c0002t0001g0042others(2): Show | 5 | HG00639.hp1 NA19043.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-90296delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17597430 | |||||
| chrX:17597638
|
G | C | 6 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-90104G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17597638 | ||||||
| chrX:17597735
|
A | C | 1 | a0002c0002t0001g0030 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.566-90007A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17597735 | ||||||
| chrX:17598201
|
T | C | 20 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0095others(17): Show | 20 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.566-89541T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17598201 | ||||||
| chrX:17598599
|
G | A | 1 | a0002c0002t0001g0054 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.566-89143G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17598599 | ||||||
| chrX:17598604
|
C | G | 15 | a0001c0001t0001g0127a0001c0001t0002g0085a0001c0001t0005g0103others(12): Show | 15 | HG01952.hp1 HG02622.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.566-89138C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17598604 | ||||||
| chrX:17598822
|
T | C | 109 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0041others(106): Show | 109 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.566-88920T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17598822 | ||||||
| chrX:17598959
|
G | T | 2 | a0001c0001t0001g0124a0001c0001t0013g0059 | 2 | HG01943.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.566-88783G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17598959 | ||||||
| chrX:17598986
|
G | A | 9 | a0001c0001t0001g0127a0002c0002t0001g0072a0002c0002t0001g0075others(6): Show | 9 | HG01952.hp1 HG02922.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-88756G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17598986 | ||||||
| chrX:17599422
|
A | AT | 3 | a0001c0001t0002g0093a0001c0001t0002g0126a0002c0002t0001g0091 | 3 | HG01069.hp1 HG01071.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.566-88310dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17599422 | |||||
| chrX:17599712
|
G | A | 1 | a0002c0002t0001g0062 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.566-88030G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17599712 | ||||||
| chrX:17600150
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0006g0112 | 2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.566-87592G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17600150 | ||||||
| chrX:17600286
|
C | CAG | 22 | a0001c0001t0001g0029a0001c0001t0001g0127a0001c0001t0002g0085others(19): Show | 22 | HG00280.hp1 HG01952.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.566-87429_566-8742 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17600286 | |||||
| chrX:17600296
|
G | C | 11 | a0001c0001t0009g0125a0001c0003t0002g0019a0001c0003t0002g0128others(8): Show | 11 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.566-87446G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17600296 | ||||||
| chrX:17600311
|
A | T | 1 | a0001c0001t0002g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.566-87431A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17600311 | ||||||
| chrX:17600509
|
A | G | 13 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0009g0125others(10): Show | 13 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.566-87233A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17600509 | ||||||
| chrX:17600770
|
C | T | 90 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0048others(87): Show | 90 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.566-86972C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17600770 | ||||||
| chrX:17600965
|
A | G | 1 | a0002c0002t0016g0005 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.566-86777A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17600965 | ||||||
| chrX:17601008
|
G | A | 1 | a0002c0002t0001g0011 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.566-86734G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17601008 | ||||||
| chrX:17601049
|
C | G | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.566-86693C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17601049 | ||||||
| chrX:17601257
|
A | G | 12 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(9): Show | 12 | HG01952.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-86485A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17601257 | ||||||
| chrX:17601390
|
T | C | 1 | a0001c0001t0002g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.566-86352T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17601390 | ||||||
| chrX:17601437
|
A | G | 1 | a0001c0003t0002g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.566-86305A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17601437 | ||||||
| chrX:17601508
|
C | T | 6 | a0002c0002t0001g0072a0002c0002t0001g0075a0002c0002t0001g0080others(3): Show | 6 | HG01952.hp1 HG03017.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-86234C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17601508 | ||||||
| chrX:17601691
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.566-86051T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17601691 | ||||||
| chrX:17602182
|
CACA | C | 10 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0009g0122others(7): Show | 10 | HG01952.hp1 HG02615.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.566-85543_566-8554 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17602182 | |||||
| chrX:17602196
|
CAACA | C | 2 | a0001c0003t0002g0142a0006c0007t0002g0115 | 2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.566-85527_566-8552 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17602196 | |||||
| chrX:17602315
|
A | C | 12 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(9): Show | 12 | HG01952.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-85427A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17602315 | ||||||
| chrX:17602684
|
C | CT | 6 | a0002c0002t0001g0072a0002c0002t0001g0075a0002c0002t0001g0080others(3): Show | 6 | HG01952.hp1 HG03017.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-85047dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17602684 | |||||
| chrX:17602749
|
G | A | 122 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0041others(119): Show | 122 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.566-84993G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17602749 | ||||||
| chrX:17602809
|
T | C | 13 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0009g0125others(10): Show | 13 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.566-84933T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17602809 | ||||||
| chrX:17602834
|
A | AT | 12 | a0001c0001t0002g0121a0001c0001t0002g0126a0001c0001t0004g0058others(9): Show | 12 | HG01071.hp1 HG01071.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-84885dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17602834 | |||||
| chrX:17602834
|
A | ATT | 8 | a0001c0001t0001g0041a0001c0001t0002g0043a0001c0001t0002g0146others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-84886_566-8488 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17602834 | |||||
| chrX:17602834
|
A | ATTT | 5 | a0001c0003t0002g0019a0001c0003t0002g0128a0001c0003t0002g0155others(2): Show | 5 | HG01258.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-84887_566-8488 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17602834 | |||||
| chrX:17602834
|
A | ATTTT | 1 | a0001c0003t0002g0142 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.566-84888_566-8488 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17602834 | |||||
| chrX:17602834
|
AT | A | 18 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0029others(15): Show | 18 | HG01074.hp1 HG02040.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.566-84885delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17602834 | |||||
| chrX:17602834
|
ATTT | A | 3 | a0002c0002t0001g0075a0002c0002t0001g0080a0003c0004t0001g0132 | 3 | HG01952.hp1 HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.566-84887_566-8488 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17602834 | |||||
| chrX:17602834
|
ATTTT | A | 3 | a0002c0002t0001g0072a0003c0004t0001g0149a0010c0012t0001g0150 | 3 | HG03017.hp1 NA18948.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.566-84888_566-8488 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17602834 | |||||
| chrX:17602939
|
C | G | 4 | a0001c0001t0001g0135a0001c0001t0001g0151a0002c0002t0001g0138others(1): Show | 4 | HG00408.hp1 HG02074.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-84803C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17602939 | ||||||
| chrX:17603184
|
T | TG | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.566-84551dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17603184 | |||||
| chrX:17603221
|
G | A | 39 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0095others(36): Show | 39 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.566-84521G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17603221 | ||||||
| chrX:17603295
|
G | A | 6 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-84447G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17603295 | ||||||
| chrX:17603557
|
A | G | 12 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0099others(9): Show | 12 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-84185A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17603557 | ||||||
| chrX:17603699
|
C | T | 12 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(9): Show | 12 | HG01952.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-84043C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17603699 | ||||||
| chrX:17603882
|
A | G | 12 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(9): Show | 12 | HG01952.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-83860A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17603882 | ||||||
| chrX:17603949
|
C | T | 6 | a0002c0002t0001g0072a0002c0002t0001g0075a0002c0002t0001g0080others(3): Show | 6 | HG01952.hp1 HG03017.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-83793C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17603949 | ||||||
| chrX:17604134
|
A | T | 12 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(9): Show | 12 | HG01952.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-83608A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17604134 | ||||||
| chrX:17604228
|
T | TCA | 15 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0099others(12): Show | 15 | HG01106.hp1 HG01243.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-83475_566-8347 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | |||||
| chrX:17604228
|
T | TCACA | 7 | a0001c0001t0002g0116a0001c0001t0002g0121a0001c0001t0002g0143others(4): Show | 7 | HG02074.hp1 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.566-83477_566-8347 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | |||||
| chrX:17604228
|
T | TCACACA | 12 | a0001c0001t0001g0041a0001c0001t0002g0120a0001c0001t0009g0125others(9): Show | 12 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-83479_566-8347 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | |||||
| chrX:17604228
|
T | TCACACAC others(3): Show |
1 | a0001c0001t0002g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.566-83483_566-8347 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | |||||
| chrX:17604228
|
T | TCACACAC others(5): Show |
2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-83485_566-8347 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | |||||
| chrX:17604228
|
T | TCACACAC others(7): Show |
1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.566-83487_566-8347 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | |||||
| chrX:17604228
|
TCA | T | 47 | a0001c0001t0001g0048a0001c0001t0001g0067a0001c0001t0001g0068others(44): Show | 47 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.566-83475_566-8347 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | |||||
| chrX:17604228
|
TCACA | T | 2 | a0001c0001t0001g0026a0011c0013t0001g0039 | 2 | NA18747.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.566-83477_566-8347 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | |||||
| chrX:17604228
|
TCACACA | T | 11 | a0001c0001t0005g0111a0001c0003t0002g0101a0002c0002t0001g0034others(8): Show | 11 | HG01952.hp1 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-83479_566-8347 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | |||||
| chrX:17604228
|
TCACACAC others(1): Show |
T | 1 | a0001c0001t0002g0085 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.566-83481_566-8347 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | |||||
| chrX:17604228
|
TCACACAC others(7): Show |
T | 1 | a0001c0001t0005g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.566-83487_566-8347 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | |||||
| chrX:17605093
|
T | C | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.566-82649T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17605093 | ||||||
| chrX:17605417
|
A | G | 6 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-82325A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17605417 | ||||||
| chrX:17606098
|
C | T | 2 | a0001c0001t0002g0004a0001c0001t0007g0073 | 2 | HG02809.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.566-81644C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17606098 | ||||||
| chrX:17606421
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.566-81321C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17606421 | ||||||
| chrX:17606751
|
G | A | 18 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0043others(15): Show | 18 | HG01109.hp1 HG01243.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.566-80991G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17606751 | ||||||
| chrX:17606840
|
G | A | 6 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-80902G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17606840 | ||||||
| chrX:17606870
|
G | C | 2 | a0001c0001t0012g0044a0001c0001t0017g0154 | 2 | HG01975.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.566-80872G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17606870 | ||||||
| chrX:17607022
|
G | A | 2 | a0002c0002t0001g0035a0002c0002t0001g0141 | 2 | HG03942.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.566-80720G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17607022 | ||||||
| chrX:17607495
|
G | A | 1 | a0004c0005t0010g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.566-80247G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17607495 | ||||||
| chrX:17607511
|
G | T | 1 | a0001c0001t0015g0079 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.566-80231G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17607511 | ||||||
| chrX:17607789
|
TA | T | 1 | a0002c0002t0001g0088 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.566-79950delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17607789 | |||||
| chrX:17607905
|
T | C | 3 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110 | 3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.566-79837T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17607905 | ||||||
| chrX:17607919
|
C | CT | 4 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0004g0069others(1): Show | 4 | HG02965.hp1 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-79806dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17607919 | |||||
| chrX:17607919
|
CT | C | 14 | a0001c0001t0001g0036a0001c0001t0002g0085a0001c0001t0005g0103others(11): Show | 14 | HG01258.hp1 HG01975.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.566-79806delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17607919 | |||||
| chrX:17607926
|
T | TC | 1 | a0001c0001t0002g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.566-79816_566-7981 others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17607926 | ||||||
| chrX:17607980
|
A | C | 7 | a0001c0001t0001g0041a0001c0001t0002g0121a0004c0005t0003g0117others(4): Show | 7 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-79762A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17607980 | ||||||
| chrX:17608071
|
T | C | 1 | a0001c0001t0002g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.566-79671T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17608071 | ||||||
| chrX:17608167
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0056 | 2 | NA18988.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.566-79575C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17608167 | ||||||
| chrX:17608401
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.566-79341A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17608401 | ||||||
| chrX:17608669
|
G | T | 1 | a0001c0001t0012g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.566-79073G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17608669 | ||||||
| chrX:17608671
|
C | CT | 1 | a0002c0002t0001g0156 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.566-79057dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17608671 | |||||
| chrX:17608685
|
T | G | 26 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0137others(23): Show | 26 | HG01071.hp2 HG01109.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.566-79057T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17608685 | ||||||
| chrX:17608685
|
TG | T | 8 | a0001c0001t0002g0099a0001c0001t0002g0116a0001c0001t0002g0120others(5): Show | 8 | HG01243.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.566-79051delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17608685 | |||||
| chrX:17608687
|
G | T | 8 | a0001c0001t0002g0099a0001c0001t0002g0116a0001c0001t0002g0120others(5): Show | 8 | HG01243.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.566-79055G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17608687 | ||||||
| chrX:17608688
|
G | T | 8 | a0001c0001t0002g0099a0001c0001t0002g0116a0001c0001t0002g0120others(5): Show | 8 | HG01243.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.566-79054G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17608688 | ||||||
| chrX:17608702
|
A | G | 8 | a0001c0001t0002g0099a0001c0001t0002g0116a0001c0001t0002g0120others(5): Show | 8 | HG01243.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.566-79040A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17608702 | ||||||
| chrX:17608818
|
A | G | 4 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(1): Show | 4 | HG02258.hp1 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-78924A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17608818 | ||||||
| chrX:17609156
|
TG | T | 1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.566-78585delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17609156 | ||||||
| chrX:17609658
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0056 | 2 | NA18988.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.566-78084G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17609658 | ||||||
| chrX:17609753
|
A | T | 15 | a0001c0001t0002g0004a0001c0001t0002g0093a0001c0001t0002g0096others(12): Show | 15 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-77989A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17609753 | ||||||
| chrX:17609983
|
C | T | 1 | a0002c0002t0001g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.566-77759C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17609983 | ||||||
| chrX:17610277
|
G | A | 1 | a0001c0001t0006g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.566-77465G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17610277 | ||||||
| chrX:17610499
|
T | C | 11 | a0001c0001t0001g0137a0001c0001t0002g0099a0001c0001t0002g0143others(8): Show | 11 | HG01243.hp1 HG01258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-77243T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17610499 | ||||||
| chrX:17610581
|
T | G | 2 | a0001c0001t0001g0124a0001c0001t0013g0059 | 2 | HG01943.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.566-77161T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17610581 | ||||||
| chrX:17611287
|
A | AG | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.566-76451dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17611287 | |||||
| chrX:17611300
|
C | T | 1 | a0003c0004t0001g0132 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.566-76442C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17611300 | ||||||
| chrX:17611308
|
G | A | 16 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0093others(13): Show | 16 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.566-76434G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17611308 | ||||||
| chrX:17611352
|
A | AG | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.566-76388dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17611352 | |||||
| chrX:17611459
|
C | T | 1 | a0002c0002t0001g0035 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.566-76283C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17611459 | ||||||
| chrX:17611547
|
C | CT | 2 | a0006c0008t0008g0113a0007c0009t0002g0160 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.566-76184dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17611547 | |||||
| chrX:17611547
|
CT | C | 2 | a0001c0001t0013g0059a0002c0002t0001g0040 | 2 | HG01167.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.566-76184delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17611547 | |||||
| chrX:17611628
|
C | T | 2 | a0001c0001t0017g0154a0004c0005t0010g0086 | 2 | HG01975.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.566-76114C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17611628 | ||||||
| chrX:17611919
|
T | C | 1 | a0002c0002t0016g0005 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.566-75823T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17611919 | ||||||
| chrX:17612047
|
T | C | 66 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0041others(63): Show | 66 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.566-75695T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17612047 | ||||||
| chrX:17612191
|
C | CT | 4 | a0001c0001t0001g0144a0001c0001t0002g0043a0001c0001t0002g0146others(1): Show | 4 | HG01109.hp1 HG02630.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-75537dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17612191 | |||||
| chrX:17612205
|
TG | T | 17 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0093others(14): Show | 17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.566-75534delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17612205 | |||||
| chrX:17612206
|
G | T | 49 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0041others(46): Show | 49 | HG00639.hp2 HG01071.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.566-75536G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17612206 | ||||||
| chrX:17612335
|
TC | T | 1 | a0003c0004t0001g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.566-75402delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17612335 | |||||
| chrX:17612938
|
T | G | 27 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0004others(24): Show | 27 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.566-74804T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17612938 | ||||||
| chrX:17613017
|
CT | C | 2 | a0001c0001t0001g0081a0002c0002t0001g0028 | 2 | HG01256.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.566-74710delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17613017 | |||||
| chrX:17613017
|
CTT | C | 121 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0026others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.566-74711_566-7471 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17613017 | |||||
| chrX:17613017
|
CTTT | C | 41 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0041others(38): Show | 41 | HG00639.hp2 HG01071.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.566-74712_566-7471 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17613017 | |||||
| chrX:17613417
|
C | A | 37 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0041others(34): Show | 37 | HG00639.hp2 HG01071.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.566-74325C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17613417 | ||||||
| chrX:17613761
|
T | A | 1 | a0002c0002t0001g0076 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.566-73981T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17613761 | ||||||
| chrX:17613961
|
G | A | 18 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0093others(15): Show | 18 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.566-73781G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17613961 | ||||||
| chrX:17614109
|
G | A | 1 | a0001c0001t0009g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.566-73633G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17614109 | ||||||
| chrX:17614124
|
GTC | G | 4 | a0001c0001t0002g0116a0001c0001t0009g0122a0001c0001t0012g0044others(1): Show | 4 | HG02615.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-73616_566-7361 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17614124 | |||||
| chrX:17614439
|
T | TG | 1 | a0003c0004t0001g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.566-73298dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17614439 | |||||
| chrX:17614622
|
G | C | 8 | a0001c0001t0001g0137a0001c0003t0002g0019a0001c0003t0002g0128others(5): Show | 8 | HG01258.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.566-73120G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17614622 | ||||||
| chrX:17614640
|
C | T | 1 | a0002c0002t0001g0030 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.566-73102C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17614640 | ||||||
| chrX:17614724
|
C | G | 2 | a0006c0008t0008g0113a0007c0009t0002g0160 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.566-73018C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17614724 | ||||||
| chrX:17614862
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.566-72880G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17614862 | ||||||
| chrX:17615073
|
CAT | C | 17 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0093others(14): Show | 17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.566-72656_566-7265 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615073 | |||||
| chrX:17615086
|
A | G | 4 | a0001c0001t0002g0116a0001c0001t0009g0122a0001c0001t0012g0044others(1): Show | 4 | HG02615.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-72656A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615086 | ||||||
| chrX:17615117
|
T | C | 1 | a0002c0002t0001g0105 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.566-72625T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615117 | ||||||
| chrX:17615137
|
T | TGTATATA others(28): Show |
1 | a0005c0006t0008g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.566-72593_566-7255 others(39): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615137 | |||||
| chrX:17615138
|
G | GTA | 1 | a0001c0001t0004g0058 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.566-72595_566-7259 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615138 | |||||
| chrX:17615149
|
C | T | 1 | a0001c0001t0004g0058 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.566-72593C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615149 | ||||||
| chrX:17615152
|
G | A | 9 | a0001c0001t0002g0085a0001c0001t0002g0116a0001c0001t0005g0103others(6): Show | 9 | HG02615.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.566-72590G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615152 | ||||||
| chrX:17615154
|
A | G | 1 | a0001c0001t0004g0058 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.566-72588A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615154 | ||||||
| chrX:17615170
|
T | C | 17 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0093others(14): Show | 17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.566-72572T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615170 | ||||||
| chrX:17615170
|
T | TAC | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.566-72571_566-7257 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615170 | |||||
| chrX:17615181
|
AT | A | 17 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0093others(14): Show | 17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.566-72560delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615181 | ||||||
| chrX:17615183
|
A | AC | 115 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(112): Show | 115 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.566-72559_566-7255 others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615183 | ||||||
| chrX:17615183
|
A | ACGTATAT others(26): Show |
3 | a0002c0002t0001g0053a0003c0004t0001g0055a0003c0004t0001g0066 | 3 | NA18966.hp1 NA19007.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.566-72559_566-7255 others(37): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615183 | ||||||
| chrX:17615183
|
A | C | 17 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0093others(14): Show | 17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.566-72559A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615183 | ||||||
| chrX:17615187
|
TATATACA others(1): Show |
T | 17 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0093others(14): Show | 17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.566-72549_566-7254 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615187 | |||||
| chrX:17615195
|
C | CATATATA others(27): Show |
23 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(20): Show | 23 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.566-72526_566-7249 others(38): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615195 | |||||
| chrX:17615203
|
C | CGTATATA others(25): Show |
1 | a0001c0001t0001g0095 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.566-72527_566-7252 others(36): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615203 | |||||
| chrX:17615204
|
G | GTA | 13 | a0001c0001t0001g0009a0001c0001t0001g0050a0001c0001t0001g0061others(10): Show | 13 | HG00408.hp1 HG02040.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.566-72529_566-7252 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615204 | |||||
| chrX:17615216
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-72526G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615216 | ||||||
| chrX:17615227
|
CAT | C | 17 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0093others(14): Show | 17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.566-72507_566-7250 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615227 | |||||
| chrX:17615229
|
T | TATATATA others(13): Show |
11 | a0001c0001t0002g0085a0001c0001t0002g0116a0001c0001t0005g0103others(8): Show | 11 | HG01975.hp1 HG02615.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-72496_566-7249 others(24): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615229 | |||||
| chrX:17615261
|
C | CATATAT | 13 | a0001c0001t0002g0002a0001c0001t0002g0096a0001c0001t0002g0106others(10): Show | 13 | HG01106.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.566-72470_566-7246 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615261 | |||||
| chrX:17615261
|
C | CATATATA others(5): Show |
4 | a0001c0001t0002g0004a0001c0001t0002g0093a0001c0001t0002g0126others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-72476_566-7246 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615261 | |||||
| chrX:17615263
|
T | C | 5 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(2): Show | 5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-72479T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615263 | ||||||
| chrX:17615419
|
A | AT | 1 | a0002c0002t0006g0060 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.566-72310dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615419 | |||||
| chrX:17615779
|
A | AC | 9 | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0052others(6): Show | 9 | HG02145.hp1 HG03688.hp1 NA18994.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-71956dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615779 | |||||
| chrX:17616087
|
AT | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0049others(1): Show | 4 | HG02071.hp1 NA18961.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-71654delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17616087 | ||||||
| chrX:17616143
|
G | A | 1 | a0004c0005t0010g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.566-71599G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17616143 | ||||||
| chrX:17616143
|
G | T | 1 | a0001c0001t0001g0070 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.566-71599G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17616143 | ||||||
| chrX:17616144
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.566-71598C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17616144 | ||||||
| chrX:17616703
|
A | G | 25 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0004others(22): Show | 25 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-71039A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17616703 | ||||||
| chrX:17616753
|
A | C | 1 | a0007c0009t0002g0160 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.566-70989A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17616753 | ||||||
| chrX:17616901
|
C | T | 1 | a0002c0002t0011g0020 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.566-70841C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17616901 | ||||||
| chrX:17617209
|
G | A | 1 | a0002c0015t0001g0046 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.566-70533G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17617209 | ||||||
| chrX:17617485
|
G | A | 5 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(2): Show | 5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-70257G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17617485 | ||||||
| chrX:17617757
|
A | C | 1 | a0004c0005t0010g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.566-69985A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17617757 | ||||||
| chrX:17618166
|
T | C | 7 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0002g0085others(4): Show | 7 | HG02622.hp2 HG02922.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-69576T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17618166 | ||||||
| chrX:17618757
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.566-68985A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17618757 | ||||||
| chrX:17618884
|
T | C | 11 | a0001c0001t0001g0137a0001c0001t0002g0099a0001c0001t0002g0143others(8): Show | 11 | HG01243.hp1 HG01258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-68858T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17618884 | ||||||
| chrX:17618885
|
C | T | 4 | a0001c0001t0009g0125a0004c0005t0003g0100a0004c0005t0003g0136others(1): Show | 4 | HG01071.hp2 HG02055.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-68857C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17618885 | ||||||
| chrX:17619311
|
ATCTCAGC others(725): Show |
A | 3 | a0001c0001t0002g0099a0001c0001t0002g0143a0008c0010t0003g0158 | 3 | HG01243.hp1 HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.566-68430_566-6769 others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17619311 | ||||||
| chrX:17619621
|
T | C | 24 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0004others(21): Show | 24 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.566-68121T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17619621 | ||||||
| chrX:17619661
|
A | G | 1 | a0001c0003t0002g0155 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.566-68081A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17619661 | ||||||
| chrX:17619805
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.566-67937C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17619805 | ||||||
| chrX:17619959
|
G | A | 4 | a0001c0001t0005g0103a0001c0001t0005g0111a0001c0003t0002g0101others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-67783G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17619959 | ||||||
| chrX:17620033
|
A | G | 2 | a0002c0002t0001g0018a0002c0002t0001g0123 | 2 | HG00639.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.566-67709A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17620033 | ||||||
| chrX:17620044
|
A | C | 3 | a0001c0001t0002g0099a0001c0001t0002g0143a0008c0010t0003g0158 | 3 | HG01243.hp1 HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.566-67698A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17620044 | ||||||
| chrX:17620596
|
G | GA | 3 | a0001c0001t0002g0043a0001c0001t0002g0146a0001c0001t0002g0164 | 3 | HG01109.hp1 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.566-67133dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17620596 | |||||
| chrX:17620596
|
GA | G | 25 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0085others(22): Show | 25 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-67133delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17620596 | |||||
| chrX:17620750
|
G | A | 1 | a0001c0001t0001g0009 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.566-66992G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17620750 | ||||||
| chrX:17620786
|
G | C | 38 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0137others(35): Show | 38 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.566-66956G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17620786 | ||||||
| chrX:17621573
|
GTAAA | G | 1 | a0002c0002t0001g0033 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.566-66166_566-6616 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17621573 | |||||
| chrX:17621619
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-66123G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17621619 | ||||||
| chrX:17621788
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.566-65954G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17621788 | ||||||
| chrX:17622114
|
C | T | 1 | a0001c0003t0002g0101 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.566-65628C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17622114 | ||||||
| chrX:17622130
|
C | G | 6 | a0001c0003t0002g0019a0001c0003t0002g0128a0001c0003t0002g0142others(3): Show | 6 | HG01258.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-65612C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17622130 | ||||||
| chrX:17622372
|
G | A | 1 | a0002c0002t0001g0082 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.566-65370G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17622372 | ||||||
| chrX:17622937
|
T | A | 2 | a0001c0001t0002g0093a0001c0001t0002g0126 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.566-64805T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17622937 | ||||||
| chrX:17623019
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.566-64723C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17623019 | ||||||
| chrX:17623425
|
C | T | 75 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(72): Show | 75 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.566-64317C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17623425 | ||||||
| chrX:17623910
|
T | C | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.566-63832T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17623910 | ||||||
| chrX:17624370
|
A | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0049others(1): Show | 4 | HG02071.hp1 NA18961.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-63372A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17624370 | ||||||
| chrX:17626249
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.566-61493C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17626249 | ||||||
| chrX:17626774
|
C | CA | 1 | a0002c0002t0001g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.566-60963dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17626774 | |||||
| chrX:17626823
|
C | T | 73 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(70): Show | 73 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.566-60919C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17626823 | ||||||
| chrX:17626926
|
TCTTA | T | 1 | a0002c0015t0001g0046 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.566-60811_566-6080 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17626926 | |||||
| chrX:17627175
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.566-60567G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17627175 | ||||||
| chrX:17627573
|
C | T | 80 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(77): Show | 80 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.566-60169C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17627573 | ||||||
| chrX:17627635
|
A | C | 1 | a0002c0002t0001g0091 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.566-60107A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17627635 | ||||||
| chrX:17627860
|
C | T | 1 | a0002c0015t0001g0046 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.566-59882C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17627860 | ||||||
| chrX:17628066
|
G | A | 2 | a0002c0002t0001g0035a0002c0002t0001g0141 | 2 | HG03942.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.566-59676G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17628066 | ||||||
| chrX:17628314
|
T | A | 1 | a0002c0002t0001g0075 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.566-59428T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17628314 | ||||||
| chrX:17628317
|
T | TC | 1 | a0001c0001t0001g0144 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.566-59422dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17628317 | |||||
| chrX:17628736
|
C | A | 73 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(70): Show | 73 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.566-59006C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17628736 | ||||||
| chrX:17629729
|
TG | T | 1 | a0001c0001t0009g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.566-58010delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17629729 | |||||
| chrX:17629922
|
G | A | 20 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0085others(17): Show | 20 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.566-57820G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17629922 | ||||||
| chrX:17630011
|
C | T | 83 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(80): Show | 83 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.566-57731C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17630011 | ||||||
| chrX:17630045
|
C | T | 25 | a0001c0001t0001g0067a0001c0001t0001g0145a0001c0001t0002g0002others(22): Show | 25 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-57697C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17630045 | ||||||
| chrX:17630182
|
G | T | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.566-57560G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17630182 | ||||||
| chrX:17630481
|
G | A | 78 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(75): Show | 78 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.566-57261G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17630481 | ||||||
| chrX:17630575
|
C | G | 81 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(78): Show | 81 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.566-57167C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17630575 | ||||||
| chrX:17630638
|
C | A | 1 | a0001c0001t0006g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.566-57104C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17630638 | ||||||
| chrX:17630946
|
G | A | 2 | a0002c0002t0001g0076a0002c0002t0001g0131 | 2 | HG02602.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.566-56796G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17630946 | ||||||
| chrX:17632082
|
G | T | 15 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0093others(12): Show | 15 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-55660G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17632082 | ||||||
| chrX:17632191
|
T | C | 1 | a0002c0002t0001g0023 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.566-55551T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17632191 | ||||||
| chrX:17632263
|
T | C | 62 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(59): Show | 62 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.566-55479T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17632263 | ||||||
| chrX:17632354
|
A | AT | 2 | a0001c0001t0001g0090a0002c0002t0001g0035 | 2 | HG04115.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.566-55379dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17632354 | |||||
| chrX:17632380
|
G | GT | 2 | a0001c0001t0001g0144a0001c0001t0012g0044 | 2 | NA18994.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.566-55350dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17632380 | |||||
| chrX:17632608
|
C | CA | 2 | a0002c0002t0001g0077a0002c0002t0001g0082 | 2 | HG02293.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.566-55125dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17632608 | |||||
| chrX:17632608
|
CA | C | 76 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(73): Show | 76 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.566-55125delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17632608 | |||||
| chrX:17633080
|
G | GT | 10 | a0001c0001t0001g0041a0001c0001t0001g0137a0001c0001t0002g0085others(7): Show | 10 | HG01258.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-54651dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17633080 | |||||
| chrX:17633163
|
A | G | 1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.566-54579A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17633163 | ||||||
| chrX:17633233
|
T | C | 1 | a0002c0002t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.566-54509T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17633233 | ||||||
| chrX:17633718
|
G | C | 1 | a0006c0008t0001g0114 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.566-54024G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17633718 | ||||||
| chrX:17634658
|
C | T | 1 | a0002c0002t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.566-53084C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17634658 | ||||||
| chrX:17634771
|
G | A | 3 | a0001c0001t0002g0116a0001c0001t0009g0122a0013c0016t0002g0119 | 3 | HG02615.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566-52971G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17634771 | ||||||
| chrX:17634826
|
C | T | 73 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(70): Show | 73 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.566-52916C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17634826 | ||||||
| chrX:17634854
|
C | T | 5 | a0001c0001t0001g0029a0002c0002t0001g0015a0002c0002t0001g0023others(2): Show | 5 | HG02027.hp1 HG02083.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-52888C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17634854 | ||||||
| chrX:17635360
|
C | A | 20 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0085others(17): Show | 20 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.566-52382C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17635360 | ||||||
| chrX:17635422
|
T | G | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.566-52320T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17635422 | ||||||
| chrX:17635451
|
T | TC | 1 | a0001c0001t0006g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.566-52284dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17635451 | |||||
| chrX:17635479
|
C | G | 20 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0085others(17): Show | 20 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.566-52263C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17635479 | ||||||
| chrX:17635660
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-52082C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17635660 | ||||||
| chrX:17635668
|
G | T | 3 | a0001c0001t0002g0116a0001c0001t0009g0122a0013c0016t0002g0119 | 3 | HG02615.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566-52074G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17635668 | ||||||
| chrX:17635940
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-51802G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17635940 | ||||||
| chrX:17635943
|
C | T | 1 | a0002c0002t0001g0047 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.566-51799C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17635943 | ||||||
| chrX:17635949
|
T | C | 1 | a0001c0001t0002g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.566-51793T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17635949 | ||||||
| chrX:17636169
|
A | G | 1 | a0001c0001t0012g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.566-51573A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17636169 | ||||||
| chrX:17636511
|
G | A | 1 | a0001c0003t0002g0155 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.566-51231G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17636511 | ||||||
| chrX:17636781
|
G | A | 1 | a0001c0001t0012g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.566-50961G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17636781 | ||||||
| chrX:17636826
|
A | G | 1 | a0004c0005t0010g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.566-50916A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17636826 | ||||||
| chrX:17636855
|
T | C | 1 | a0002c0002t0001g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.566-50887T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17636855 | ||||||
| chrX:17636916
|
TATC | T | 1 | a0001c0001t0001g0081 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.566-50823_566-5082 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17636916 | |||||
| chrX:17636941
|
C | A | 73 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(70): Show | 73 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.566-50801C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17636941 | ||||||
| chrX:17637070
|
C | T | 1 | a0002c0002t0001g0033 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.566-50672C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17637070 | ||||||
| chrX:17637342
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0049others(1): Show | 4 | HG02071.hp1 NA18961.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-50400G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17637342 | ||||||
| chrX:17637394
|
C | CG | 1 | a0001c0001t0001g0049 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.566-50343dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17637394 | |||||
| chrX:17637397
|
GGGT | G | 1 | a0001c0001t0001g0026 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.566-50334_566-5033 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17637397 | |||||
| chrX:17637660
|
G | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-50082G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17637660 | ||||||
| chrX:17637680
|
C | G | 8 | a0001c0001t0002g0085a0001c0001t0002g0116a0001c0001t0005g0103others(5): Show | 8 | HG02615.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.566-50062C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17637680 | ||||||
| chrX:17638000
|
A | G | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.566-49742A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17638000 | ||||||
| chrX:17638289
|
G | A | 1 | a0001c0003t0002g0155 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.566-49453G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17638289 | ||||||
| chrX:17638746
|
AG | A | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.566-48995delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17638746 | ||||||
| chrX:17638965
|
G | A | 2 | a0002c0002t0001g0035a0002c0002t0001g0141 | 2 | HG03942.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.566-48777G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17638965 | ||||||
| chrX:17639273
|
T | G | 2 | a0001c0001t0002g0096a0004c0005t0003g0117 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.566-48469T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17639273 | ||||||
| chrX:17639318
|
C | A | 3 | a0001c0001t0002g0116a0001c0001t0009g0122a0013c0016t0002g0119 | 3 | HG02615.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566-48424C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17639318 | ||||||
| chrX:17639325
|
A | G | 2 | a0001c0001t0001g0135a0002c0002t0001g0011 | 2 | NA19067.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.566-48417A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17639325 | ||||||
| chrX:17639544
|
TATAAC | T | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.566-48194_566-4819 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17639544 | |||||
| chrX:17640178
|
G | A | 1 | a0004c0005t0003g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.566-47564G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17640178 | ||||||
| chrX:17640263
|
A | G | 2 | a0001c0001t0002g0043a0001c0001t0002g0146 | 2 | HG01109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.566-47479A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17640263 | ||||||
| chrX:17640823
|
C | T | 1 | a0002c0002t0001g0040 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.566-46919C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17640823 | ||||||
| chrX:17641321
|
C | T | 15 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0093others(12): Show | 15 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-46421C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17641321 | ||||||
| chrX:17641370
|
T | A | 1 | a0001c0001t0012g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.566-46372T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17641370 | ||||||
| chrX:17641702
|
C | A | 1 | a0001c0001t0001g0144 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.566-46040C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17641702 | ||||||
| chrX:17641762
|
TA | T | 25 | a0001c0001t0001g0029a0001c0001t0001g0041a0001c0001t0001g0095others(22): Show | 25 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-45967delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17641762 | |||||
| chrX:17641762
|
TAA | T | 3 | a0001c0001t0002g0116a0001c0001t0009g0122a0013c0016t0002g0119 | 3 | HG02615.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566-45968_566-4596 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17641762 | |||||
| chrX:17641848
|
G | C | 3 | a0001c0001t0002g0116a0001c0001t0009g0122a0013c0016t0002g0119 | 3 | HG02615.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566-45894G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17641848 | ||||||
| chrX:17642497
|
A | G | 26 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0004others(23): Show | 26 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.566-45245A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17642497 | ||||||
| chrX:17642655
|
C | A | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.566-45087C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17642655 | ||||||
| chrX:17643258
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-44484C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17643258 | ||||||
| chrX:17643264
|
T | A | 2 | a0002c0002t0001g0008a0002c0002t0001g0040 | 2 | HG01167.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.566-44478T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17643264 | ||||||
| chrX:17643322
|
G | A | 5 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(2): Show | 5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-44420G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17643322 | ||||||
| chrX:17643596
|
C | G | 1 | a0002c0002t0001g0021 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.566-44146C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17643596 | ||||||
| chrX:17644517
|
C | T | 1 | a0002c0002t0001g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.566-43225C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17644517 | ||||||
| chrX:17645633
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-42109A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17645633 | ||||||
| chrX:17646663
|
T | C | 1 | a0002c0002t0001g0053 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.566-41079T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17646663 | ||||||
| chrX:17646918
|
G | A | 1 | a0002c0002t0001g0091 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.566-40824G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17646918 | ||||||
| chrX:17647047
|
A | AT | 5 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(2): Show | 5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-40688dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17647047 | |||||
| chrX:17647649
|
C | T | 2 | a0001c0001t0002g0043a0001c0001t0002g0146 | 2 | HG01109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.566-40093C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17647649 | ||||||
| chrX:17647947
|
C | T | 5 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(2): Show | 5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-39795C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17647947 | ||||||
| chrX:17647948
|
G | A | 5 | a0002c0002t0001g0025a0002c0002t0001g0030a0002c0002t0001g0031others(2): Show | 5 | HG00642.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-39794G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17647948 | ||||||
| chrX:17647980
|
CT | C | 73 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(70): Show | 73 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.566-39750delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17647980 | |||||
| chrX:17648432
|
C | A | 1 | a0002c0002t0001g0139 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.566-39310C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17648432 | ||||||
| chrX:17649637
|
G | A | 15 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0093others(12): Show | 15 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-38105G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17649637 | ||||||
| chrX:17650046
|
C | A | 1 | a0001c0001t0001g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.566-37696C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17650046 | ||||||
| chrX:17650512
|
T | C | 1 | a0002c0002t0001g0033 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.566-37230T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17650512 | ||||||
| chrX:17650922
|
T | A | 61 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(58): Show | 61 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.566-36820T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17650922 | ||||||
| chrX:17651232
|
G | A | 8 | a0001c0001t0002g0085a0001c0001t0002g0116a0001c0001t0005g0103others(5): Show | 8 | HG02615.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.566-36510G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17651232 | ||||||
| chrX:17651243
|
TAGA | T | 15 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0093others(12): Show | 15 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-36493_566-3649 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17651243 | |||||
| chrX:17651394
|
T | G | 1 | a0011c0013t0001g0039 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.566-36348T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17651394 | ||||||
| chrX:17651589
|
G | A | 2 | a0002c0002t0001g0032a0002c0002t0001g0077 | 2 | HG01099.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.566-36153G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17651589 | ||||||
| chrX:17651660
|
C | G | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.566-36082C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17651660 | ||||||
| chrX:17651918
|
T | G | 1 | a0004c0005t0010g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.566-35824T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17651918 | ||||||
| chrX:17652078
|
C | G | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.566-35664C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17652078 | ||||||
| chrX:17652273
|
G | A | 1 | a0001c0001t0004g0058 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.566-35469G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17652273 | ||||||
| chrX:17652401
|
T | A | 16 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0093others(13): Show | 16 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.566-35341T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17652401 | ||||||
| chrX:17652417
|
G | T | 1 | a0002c0002t0001g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.566-35325G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17652417 | ||||||
| chrX:17653424
|
C | CT | 1 | a0001c0003t0002g0142 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.566-34304dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17653424 | |||||
| chrX:17653424
|
CT | C | 4 | a0001c0001t0001g0029a0001c0001t0001g0070a0002c0002t0001g0091others(1): Show | 4 | HG02698.hp1 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-34304delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17653424 | |||||
| chrX:17653576
|
T | C | 1 | a0002c0002t0001g0003 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.566-34166T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17653576 | ||||||
| chrX:17653918
|
C | T | 2 | a0002c0002t0001g0017a0002c0002t0001g0074 | 2 | HG01358.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.566-33824C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17653918 | ||||||
| chrX:17653927
|
G | GCTGC | 1 | a0001c0001t0001g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.566-33813_566-3381 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17653927 | |||||
| chrX:17654079
|
A | AG | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.566-33662dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17654079 | |||||
| chrX:17654486
|
A | G | 1 | a0002c0002t0001g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.566-33256A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17654486 | ||||||
| chrX:17655116
|
C | T | 3 | a0001c0001t0002g0116a0001c0001t0009g0122a0013c0016t0002g0119 | 3 | HG02615.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566-32626C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17655116 | ||||||
| chrX:17655379
|
A | G | 1 | a0002c0002t0001g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.566-32363A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17655379 | ||||||
| chrX:17655387
|
CA | C | 1 | a0002c0002t0001g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.566-32354delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17655387 | ||||||
| chrX:17655390
|
A | G | 1 | a0002c0002t0001g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.566-32352A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17655390 | ||||||
| chrX:17655570
|
G | T | 10 | a0001c0001t0001g0067a0001c0001t0001g0145a0001c0001t0007g0073others(7): Show | 10 | HG00639.hp2 HG01952.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-32172G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17655570 | ||||||
| chrX:17655703
|
A | G | 10 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0002g0085others(7): Show | 10 | HG02615.hp2 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.566-32039A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17655703 | ||||||
| chrX:17655872
|
A | C | 2 | a0001c0001t0001g0026a0002c0002t0001g0014 | 2 | HG00408.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.566-31870A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17655872 | ||||||
| chrX:17655993
|
A | AG | 162 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(159): Show | 162 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.566-31747dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17655993 | |||||
| chrX:17655994
|
G | GA | 2 | a0002c0002t0001g0087a0002c0002t0001g0088 | 2 | NA18945.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.566-31748_566-3174 others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17655994 | ||||||
| chrX:17656030
|
T | G | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.566-31712T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17656030 | ||||||
| chrX:17656482
|
C | T | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.566-31260C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17656482 | ||||||
| chrX:17656728
|
C | T | 73 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(70): Show | 73 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.566-31014C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17656728 | ||||||
| chrX:17657413
|
CG | C | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.566-30328delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17657413 | ||||||
| chrX:17659229
|
G | T | 1 | a0002c0002t0001g0010 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.566-28513G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17659229 | ||||||
| chrX:17659683
|
A | T | 83 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(80): Show | 83 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.566-28059A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17659683 | ||||||
| chrX:17659759
|
C | T | 2 | a0006c0008t0008g0113a0007c0009t0002g0160 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.566-27983C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17659759 | ||||||
| chrX:17659909
|
C | T | 1 | a0001c0001t0013g0059 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.566-27833C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17659909 | ||||||
| chrX:17660000
|
T | C | 1 | a0002c0002t0001g0084 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.566-27742T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17660000 | ||||||
| chrX:17660147
|
G | A | 75 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(72): Show | 75 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.566-27595G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17660147 | ||||||
| chrX:17660168
|
C | T | 1 | a0002c0002t0001g0078 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.566-27574C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17660168 | ||||||
| chrX:17660346
|
C | T | 15 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0036others(12): Show | 15 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-27396C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17660346 | ||||||
| chrX:17660374
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.566-27368C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17660374 | ||||||
| chrX:17660660
|
A | G | 1 | a0001c0001t0015g0079 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.566-27082A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17660660 | ||||||
| chrX:17660995
|
A | G | 2 | a0006c0008t0008g0113a0007c0009t0002g0160 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.566-26747A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17660995 | ||||||
| chrX:17661229
|
A | G | 5 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(2): Show | 5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-26513A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17661229 | ||||||
| chrX:17661448
|
C | T | 3 | a0001c0001t0002g0116a0001c0001t0009g0122a0013c0016t0002g0119 | 3 | HG02615.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566-26294C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17661448 | ||||||
| chrX:17661761
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.566-25981C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17661761 | ||||||
| chrX:17661883
|
G | A | 25 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0004others(22): Show | 25 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-25859G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17661883 | ||||||
| chrX:17662034
|
C | T | 1 | a0002c0002t0001g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.566-25708C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17662034 | ||||||
| chrX:17662331
|
T | C | 1 | a0002c0002t0001g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.566-25411T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17662331 | ||||||
| chrX:17663168
|
A | G | 2 | a0001c0001t0017g0154a0004c0005t0010g0086 | 2 | HG01975.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.566-24574A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17663168 | ||||||
| chrX:17663492
|
A | T | 4 | a0001c0001t0009g0125a0004c0005t0003g0117a0004c0005t0003g0136others(1): Show | 4 | HG01071.hp2 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-24250A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17663492 | ||||||
| chrX:17664035
|
C | CT | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.566-23704dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17664035 | |||||
| chrX:17664147
|
G | T | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.566-23595G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17664147 | ||||||
| chrX:17664148
|
C | G | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.566-23594C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17664148 | ||||||
| chrX:17664207
|
A | AT | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.566-23533dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17664207 | |||||
| chrX:17664246
|
A | T | 1 | a0002c0002t0001g0080 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.566-23496A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17664246 | ||||||
| chrX:17664248
|
G | T | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.566-23494G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17664248 | ||||||
| chrX:17664341
|
A | G | 2 | a0001c0001t0002g0093a0001c0001t0002g0126 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.566-23401A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17664341 | ||||||
| chrX:17664701
|
C | G | 57 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(54): Show | 57 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.566-23041C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17664701 | ||||||
| chrX:17664780
|
G | A | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.566-22962G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17664780 | ||||||
| chrX:17665042
|
A | G | 1 | a0003c0004t0001g0132 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.566-22700A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17665042 | ||||||
| chrX:17665093
|
A | T | 5 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(2): Show | 5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-22649A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17665093 | ||||||
| chrX:17665225
|
C | CT | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.566-22513dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17665225 | |||||
| chrX:17665304
|
T | C | 1 | a0002c0002t0001g0084 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.566-22438T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17665304 | ||||||
| chrX:17665318
|
A | AT | 38 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0098others(35): Show | 38 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.566-22396dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17665318 | |||||
| chrX:17665318
|
A | ATT | 7 | a0001c0001t0002g0085a0001c0001t0002g0121a0001c0001t0006g0112others(4): Show | 7 | HG00642.hp1 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-22397_566-2239 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17665318 | |||||
| chrX:17665318
|
A | ATTT | 5 | a0001c0001t0002g0002a0001c0001t0002g0107a0001c0001t0002g0110others(2): Show | 5 | HG01358.hp1 HG02293.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-22398_566-2239 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17665318 | |||||
| chrX:17665318
|
A | ATTTT | 2 | a0001c0001t0002g0106a0001c0001t0002g0120 | 2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.566-22399_566-2239 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17665318 | |||||
| chrX:17665318
|
AT | A | 49 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(46): Show | 49 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.566-22396delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17665318 | |||||
| chrX:17665318
|
ATT | A | 4 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0013g0059others(1): Show | 4 | HG02965.hp1 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-22397_566-2239 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17665318 | |||||
| chrX:17665536
|
C | T | 21 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0085others(18): Show | 21 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.566-22206C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17665536 | ||||||
| chrX:17665801
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0049 | 2 | NA18961.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.566-21941T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17665801 | ||||||
| chrX:17666420
|
G | GTATT | 24 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0085others(21): Show | 24 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.566-21320_566-2131 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17666420 | |||||
| chrX:17666654
|
GTGAA | G | 23 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0085others(20): Show | 23 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.566-21068_566-2106 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17666654 | |||||
| chrX:17666703
|
A | G | 24 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0085others(21): Show | 24 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.566-21039A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17666703 | ||||||
| chrX:17666751
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.566-20991T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17666751 | ||||||
| chrX:17666774
|
T | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-20968T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17666774 | ||||||
| chrX:17666830
|
G | A | 15 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0093others(12): Show | 15 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-20912G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17666830 | ||||||
| chrX:17667578
|
C | A | 1 | a0005c0006t0001g0157 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.566-20164C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17667578 | ||||||
| chrX:17667678
|
T | C | 2 | a0001c0001t0017g0154a0004c0005t0010g0086 | 2 | HG01975.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.566-20064T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17667678 | ||||||
| chrX:17667731
|
G | T | 10 | a0001c0001t0002g0096a0001c0001t0002g0099a0001c0001t0002g0143others(7): Show | 10 | HG01243.hp1 HG01258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.566-20011G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17667731 | ||||||
| chrX:17667939
|
A | AT | 22 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0004others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.566-19794dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17667939 | |||||
| chrX:17668088
|
T | TA | 6 | a0001c0001t0001g0153a0002c0002t0001g0010a0002c0002t0001g0031others(3): Show | 6 | HG01433.hp1 HG01928.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-19631dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17668088 | |||||
| chrX:17668088
|
T | TAA | 1 | a0002c0002t0001g0156 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.566-19632_566-1963 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17668088 | |||||
| chrX:17668088
|
TA | T | 18 | a0001c0001t0001g0135a0001c0001t0002g0085a0001c0001t0002g0096others(15): Show | 18 | HG00639.hp1 HG01074.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.566-19631delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17668088 | |||||
| chrX:17668088
|
TAA | T | 23 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0137others(20): Show | 23 | HG01071.hp1 HG01106.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.566-19632_566-1963 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17668088 | |||||
| chrX:17668088
|
TAAA | T | 2 | a0001c0001t0002g0093a0001c0003t0002g0101 | 2 | HG01069.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.566-19633_566-1963 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17668088 | |||||
| chrX:17668089
|
A | T | 1 | a0001c0001t0001g0081 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.566-19653A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17668089 | ||||||
| chrX:17668313
|
C | CA | 8 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(5): Show | 8 | HG02602.hp1 HG02622.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.566-19420dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17668313 | |||||
| chrX:17668724
|
T | A | 16 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0093others(13): Show | 16 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.566-19018T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17668724 | ||||||
| chrX:17668810
|
G | A | 3 | a0002c0002t0001g0087a0002c0002t0001g0088a0002c0002t0001g0089 | 3 | HG02129.hp1 NA18945.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.566-18932G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17668810 | ||||||
| chrX:17668919
|
G | A | 1 | a0002c0002t0001g0033 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.566-18823G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17668919 | ||||||
| chrX:17669180
|
A | G | 5 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(2): Show | 5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-18562A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17669180 | ||||||
| chrX:17669466
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.566-18276T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17669466 | ||||||
| chrX:17669647
|
G | A | 1 | a0002c0002t0001g0033 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.566-18095G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17669647 | ||||||
| chrX:17670910
|
C | A | 1 | a0001c0001t0012g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.566-16832C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17670910 | ||||||
| chrX:17671302
|
C | A | 3 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0152 | 3 | HG00642.hp1 HG01928.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.566-16440C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17671302 | ||||||
| chrX:17671394
|
C | T | 1 | a0002c0002t0001g0031 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.566-16348C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17671394 | ||||||
| chrX:17671958
|
G | A | 3 | a0001c0001t0002g0116a0001c0001t0009g0122a0013c0016t0002g0119 | 3 | HG02615.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566-15784G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17671958 | ||||||
| chrX:17672680
|
C | G | 3 | a0001c0001t0002g0004a0001c0001t0002g0093a0001c0001t0002g0126 | 3 | HG01069.hp1 HG01071.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.566-15062C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17672680 | ||||||
| chrX:17673145
|
G | GT | 4 | a0002c0002t0001g0007a0002c0002t0001g0032a0002c0002t0001g0042others(1): Show | 4 | HG01099.hp1 HG02293.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-14596dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673145 | |||||
| chrX:17673175
|
GA | G | 3 | a0001c0001t0001g0052a0002c0002t0001g0015a0002c0002t0001g0152 | 3 | HG00642.hp1 HG02083.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.566-14564delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673175 | |||||
| chrX:17673175
|
GAAAC | G | 1 | a0004c0005t0003g0117 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.566-14565_566-1456 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673175 | |||||
| chrX:17673176
|
AAAC | A | 1 | a0002c0002t0001g0010 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.566-14564_566-1456 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673176 | |||||
| chrX:17673176
|
AAACAC | A | 1 | a0001c0001t0009g0125 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.566-14564_566-1456 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673176 | |||||
| chrX:17673177
|
A | AAC | 13 | a0001c0001t0001g0061a0001c0001t0001g0081a0001c0001t0001g0090others(10): Show | 13 | HG00639.hp2 HG01071.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.566-14505_566-1450 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | |||||
| chrX:17673177
|
A | AACAC | 1 | a0001c0001t0001g0083 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.566-14507_566-1450 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | |||||
| chrX:17673177
|
A | AACACAC | 1 | a0002c0002t0001g0071 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.566-14509_566-1450 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | |||||
| chrX:17673177
|
A | AACACACA others(1): Show |
3 | a0001c0001t0009g0122a0002c0002t0001g0025a0002c0002t0001g0075 | 3 | HG02615.hp2 HG04228.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.566-14511_566-1450 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | |||||
| chrX:17673177
|
A | AACACACA others(9): Show |
1 | a0001c0001t0002g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.566-14519_566-1450 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | |||||
| chrX:17673177
|
A | ACAC | 1 | a0002c0002t0001g0076 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.566-14565_566-1456 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17673177 | ||||||
| chrX:17673177
|
AAC | A | 33 | a0001c0001t0001g0009a0001c0001t0001g0094a0001c0001t0001g0095others(30): Show | 33 | HG01099.hp1 HG01192.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.566-14505_566-1450 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | |||||
| chrX:17673177
|
AACAC | A | 16 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0137others(13): Show | 16 | HG00639.hp1 HG01074.hp1 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.566-14507_566-1450 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | |||||
| chrX:17673177
|
AACACAC | A | 13 | a0001c0001t0001g0050a0001c0001t0002g0093a0001c0001t0002g0120others(10): Show | 13 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.566-14509_566-1450 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | |||||
| chrX:17673177
|
AACACACA others(1): Show |
A | 14 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0096others(11): Show | 14 | HG01243.hp1 HG01258.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.566-14511_566-1450 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | |||||
| chrX:17673177
|
AACACACA others(3): Show |
A | 2 | a0001c0001t0002g0107a0004c0005t0010g0086 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.566-14513_566-1450 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | |||||
| chrX:17673177
|
AACACACA others(5): Show |
A | 4 | a0002c0002t0001g0008a0002c0002t0001g0035a0002c0002t0001g0141others(1): Show | 4 | HG01515.hp1 HG02257.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-14515_566-1450 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | |||||
| chrX:17673177
|
AACACACA others(7): Show |
A | 1 | a0001c0001t0012g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.566-14517_566-1450 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | |||||
| chrX:17673177
|
AACACACA others(9): Show |
A | 1 | a0001c0001t0006g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.566-14519_566-1450 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | |||||
| chrX:17673177
|
AACACACA others(11): Show |
A | 2 | a0001c0001t0001g0144a0002c0002t0001g0030 | 2 | HG01975.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.566-14521_566-1450 others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | |||||
| chrX:17673177
|
AACACACA others(15): Show |
A | 1 | a0001c0001t0001g0038 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.566-14525_566-1450 others(26): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | |||||
| chrX:17673177
|
AACACACA others(17): Show |
A | 30 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(27): Show | 30 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.566-14527_566-1450 others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | |||||
| chrX:17673237
|
C | A | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.566-14505C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17673237 | ||||||
| chrX:17673237
|
C | CACACACA others(3): Show |
1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.566-14504_566-1450 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673237 | |||||
| chrX:17673237
|
C | CACAG | 2 | a0002c0002t0001g0045a0002c0002t0001g0054 | 2 | HG00140.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.566-14504_566-1450 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673237 | |||||
| chrX:17673237
|
C | G | 23 | a0001c0001t0001g0050a0001c0001t0017g0154a0002c0002t0001g0003others(20): Show | 23 | HG00639.hp1 HG01074.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.566-14505C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17673237 | ||||||
| chrX:17673429
|
C | T | 3 | a0001c0001t0002g0004a0001c0001t0002g0093a0001c0001t0002g0126 | 3 | HG01069.hp1 HG01071.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.566-14313C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17673429 | ||||||
| chrX:17673476
|
G | A | 5 | a0003c0004t0001g0055a0003c0004t0001g0066a0003c0004t0001g0132others(2): Show | 5 | HG01952.hp1 NA18948.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-14266G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17673476 | ||||||
| chrX:17674031
|
C | T | 85 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(82): Show | 85 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.566-13711C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17674031 | ||||||
| chrX:17674142
|
C | G | 1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.566-13600C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17674142 | ||||||
| chrX:17674784
|
G | C | 1 | a0001c0001t0002g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.566-12958G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17674784 | ||||||
| chrX:17675626
|
C | T | 75 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(72): Show | 75 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.566-12116C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17675626 | ||||||
| chrX:17675929
|
A | G | 3 | a0001c0001t0002g0004a0001c0001t0002g0093a0001c0001t0002g0126 | 3 | HG01069.hp1 HG01071.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.566-11813A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17675929 | ||||||
| chrX:17676009
|
A | G | 10 | a0001c0001t0002g0096a0001c0001t0002g0099a0001c0001t0002g0143others(7): Show | 10 | HG01243.hp1 HG01258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.566-11733A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17676009 | ||||||
| chrX:17676293
|
T | C | 1 | a0002c0002t0001g0014 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.566-11449T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17676293 | ||||||
| chrX:17676788
|
C | T | 2 | a0002c0002t0001g0065a0002c0002t0001g0148 | 2 | NA19012.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.566-10954C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17676788 | ||||||
| chrX:17676895
|
G | GT | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.566-10841dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17676895 | |||||
| chrX:17677043
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.566-10699C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17677043 | ||||||
| chrX:17677070
|
C | A | 58 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(55): Show | 58 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.566-10672C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17677070 | ||||||
| chrX:17677425
|
G | GAT | 1 | a0004c0005t0010g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.566-10304_566-1030 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17677425 | |||||
| chrX:17677621
|
C | G | 1 | a0004c0005t0010g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.566-10121C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17677621 | ||||||
| chrX:17677978
|
T | TTTGTTG | 5 | a0001c0001t0002g0004a0001c0001t0002g0093a0001c0001t0002g0121others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-9743_566-9738d others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17677978 | |||||
| chrX:17678245
|
CT | C | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.566-9493delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17678245 | |||||
| chrX:17678271
|
G | GGT | 2 | a0002c0002t0001g0035a0002c0002t0001g0141 | 2 | HG03942.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.566-9449_566-9448d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17678271 | |||||
| chrX:17678271
|
G | GGTGT | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-9451_566-9448d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17678271 | |||||
| chrX:17678293
|
T | A | 3 | a0001c0001t0001g0041a0001c0001t0017g0154a0002c0002t0011g0020 | 3 | HG01975.hp1 HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.566-9449T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17678293 | ||||||
| chrX:17678293
|
T | TGA | 12 | a0001c0001t0001g0049a0001c0001t0001g0137a0001c0001t0002g0004others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-9426_566-9425d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17678293 | |||||
| chrX:17678293
|
T | TGAGA | 7 | a0001c0001t0002g0002a0001c0001t0002g0106a0001c0001t0002g0107others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.566-9428_566-9425d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17678293 | |||||
| chrX:17678293
|
T | TGTGA | 6 | a0001c0001t0002g0085a0001c0001t0005g0103a0001c0001t0005g0111others(3): Show | 6 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-9448_566-9447i others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17678293 | |||||
| chrX:17678440
|
T | G | 1 | a0001c0001t0012g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.566-9302T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17678440 | ||||||
| chrX:17678592
|
GC | G | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.566-9149delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17678592 | ||||||
| chrX:17678888
|
CT | C | 17 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0093others(14): Show | 17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.566-8853delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17678888 | ||||||
| chrX:17679228
|
A | T | 1 | a0001c0001t0001g0067 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.566-8514A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17679228 | ||||||
| chrX:17679359
|
A | G | 2 | a0001c0001t0002g0093a0001c0001t0002g0126 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.566-8383A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17679359 | ||||||
| chrX:17679399
|
A | G | 1 | a0002c0002t0001g0008 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.566-8343A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17679399 | ||||||
| chrX:17679859
|
A | AG | 18 | a0001c0001t0001g0137a0001c0001t0001g0144a0001c0001t0012g0044others(15): Show | 18 | HG00140.hp1 HG01928.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.566-7872dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17679859 | |||||
| chrX:17679859
|
A | AGG | 2 | a0001c0003t0002g0128a0001c0003t0002g0142 | 2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.566-7873_566-7872d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17679859 | |||||
| chrX:17679859
|
AG | A | 51 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0036others(48): Show | 51 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.566-7872delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17679859 | |||||
| chrX:17679859
|
AGG | A | 1 | a0004c0005t0010g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.566-7873_566-7872d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17679859 | |||||
| chrX:17679863
|
G | C | 2 | a0001c0001t0001g0127a0005c0006t0001g0162 | 2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.566-7879G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17679863 | ||||||
| chrX:17680277
|
A | G | 62 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(59): Show | 62 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.566-7465A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17680277 | ||||||
| chrX:17680693
|
C | T | 1 | a0001c0003t0002g0019 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.566-7049C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17680693 | ||||||
| chrX:17680896
|
G | A | 1 | a0002c0002t0001g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.566-6846G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17680896 | ||||||
| chrX:17681040
|
TG | T | 2 | a0004c0005t0003g0136a0012c0014t0003g0092 | 2 | HG01071.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.566-6700delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17681040 | |||||
| chrX:17681385
|
C | A | 55 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(52): Show | 55 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.566-6357C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17681385 | ||||||
| chrX:17681396
|
A | G | 1 | a0002c0002t0001g0076 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.566-6346A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17681396 | ||||||
| chrX:17681714
|
C | A | 75 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(72): Show | 75 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.566-6028C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17681714 | ||||||
| chrX:17681789
|
C | G | 5 | a0002c0002t0001g0025a0002c0002t0001g0030a0002c0002t0001g0031others(2): Show | 5 | HG00642.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-5953C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17681789 | ||||||
| chrX:17682137
|
C | T | 16 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0093others(13): Show | 16 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.566-5605C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17682137 | ||||||
| chrX:17682266
|
A | C | 22 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0085others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.566-5476A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17682266 | ||||||
| chrX:17682297
|
TAGC | T | 1 | a0002c0002t0001g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.566-5442_566-5440d others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17682297 | |||||
| chrX:17682406
|
G | T | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.566-5336G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17682406 | ||||||
| chrX:17682695
|
A | G | 4 | a0001c0001t0004g0163a0002c0002t0001g0006a0002c0002t0001g0053others(1): Show | 4 | HG01261.hp1 NA18953.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-5047A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17682695 | ||||||
| chrX:17682912
|
C | G | 85 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(82): Show | 85 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.566-4830C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17682912 | ||||||
| chrX:17682938
|
C | G | 5 | a0001c0001t0002g0002a0001c0001t0002g0106a0001c0001t0002g0107others(2): Show | 5 | HG02258.hp1 HG02293.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-4804C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17682938 | ||||||
| chrX:17683001
|
T | C | 22 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0004others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.566-4741T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17683001 | ||||||
| chrX:17683229
|
G | C | 1 | a0002c0002t0001g0138 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.566-4513G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17683229 | ||||||
| chrX:17683372
|
CTTT | C | 1 | a0004c0005t0010g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.566-4367_566-4365d others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17683372 | |||||
| chrX:17683552
|
G | C | 1 | a0002c0002t0001g0010 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.566-4190G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17683552 | ||||||
| chrX:17683797
|
C | T | 1 | a0001c0001t0004g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.566-3945C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17683797 | ||||||
| chrX:17684245
|
A | C | 3 | a0002c0002t0001g0087a0002c0002t0001g0088a0002c0002t0001g0156 | 3 | NA18945.hp1 NA19009.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.566-3497A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17684245 | ||||||
| chrX:17684886
|
T | C | 2 | a0001c0001t0001g0029a0002c0002t0001g0037 | 2 | NA18940.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.566-2856T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17684886 | ||||||
| chrX:17685166
|
C | T | 7 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0002g0085others(4): Show | 7 | HG02622.hp2 HG02717.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-2576C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17685166 | ||||||
| chrX:17685486
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-2256C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17685486 | ||||||
| chrX:17685599
|
CT | C | 13 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0043others(10): Show | 13 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.566-2134delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17685599 | |||||
| chrX:17686309
|
C | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.566-1433C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17686309 | ||||||
| chrX:17686519
|
A | G | 1 | a0002c0002t0001g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.566-1223A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17686519 | ||||||
| chrX:17687592
|
T | C | 3 | a0001c0001t0002g0116a0001c0001t0009g0122a0013c0016t0002g0119 | 3 | HG02615.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566-150T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17687592 | ||||||
| chrX:17687730
|
C | CT | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.566-10dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17687730 | |||||
| chrX:17687925
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0056 | 2 | NA18988.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.718+31G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17687925 | ||||||
| chrX:17688057
|
A | C | 1 | a0001c0001t0006g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.718+163A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17688057 | ||||||
| chrX:17688882
|
T | A | 32 | a0001c0001t0001g0067a0001c0001t0001g0137a0001c0001t0001g0145others(29): Show | 32 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.718+988T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17688882 | ||||||
| chrX:17689034
|
C | A | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.718+1140C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17689034 | ||||||
| chrX:17689309
|
A | G | 2 | a0002c0002t0001g0042a0002c0002t0001g0139 | 2 | HG00673.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.718+1415A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17689309 | ||||||
| chrX:17689329
|
T | A | 1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.718+1435T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17689329 | ||||||
| chrX:17689761
|
C | T | 28 | a0001c0001t0001g0067a0001c0001t0001g0145a0001c0001t0002g0002others(25): Show | 28 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.718+1867C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17689761 | ||||||
| chrX:17690362
|
TC | T | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.719-1970delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 17690362 | |||||
| chrX:17690427
|
G | GA | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.719-1905dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 17690427 | |||||
| chrX:17690559
|
A | ACC | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.719-1771_719-1770d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 17690559 | |||||
| chrX:17690643
|
A | T | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.719-1692A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17690643 | ||||||
| chrX:17690680
|
T | TTA | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.719-1655_719-1654i others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17690680 | ||||||
| chrX:17690682
|
A | T | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.719-1653A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17690682 | ||||||
| chrX:17690735
|
G | GA | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.719-1599dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 17690735 | |||||
| chrX:17690765
|
A | T | 1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.719-1570A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17690765 | ||||||
| chrX:17690912
|
TA | T | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.719-1420delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 17690912 | |||||
| chrX:17691125
|
T | C | 1 | a0002c0002t0001g0003 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.719-1210T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17691125 | ||||||
| chrX:17691246
|
C | A | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.719-1089C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17691246 | ||||||
| chrX:17691258
|
T | G | 1 | a0001c0001t0017g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.719-1077T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17691258 | ||||||
| chrX:17691419
|
A | G | 1 | a0001c0001t0001g0038 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.719-916A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17691419 | ||||||
| chrX:17691706
|
A | G | 85 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(82): Show | 85 | HG00609.hp1 HG00639.hp2 HG01069.hp1 others(82): Show |
intron_variant | MODIFIER | c.719-629A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17691706 | ||||||
| chrX:17691743
|
A | G | 1 | a0002c0002t0001g0040 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.719-592A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17691743 | ||||||
| chrX:17691842
|
G | C | 1 | a0001c0003t0002g0019 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.719-493G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17691842 | ||||||
| chrX:17691936
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.719-399G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17691936 | ||||||
| chrX:17692027
|
A | G | 1 | a0002c0002t0001g0010 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.719-308A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17692027 | ||||||
| chrX:17692233
|
C | CT | 1 | a0002c0002t0001g0071 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.719-88dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 17692233 | |||||
| chrX:17692233
|
CT | C | 54 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(51): Show | 54 | HG00609.hp1 HG01071.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.719-88delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 17692233 | |||||
| chrX:17692233
|
CTT | C | 24 | a0001c0001t0001g0067a0001c0001t0001g0145a0001c0001t0002g0002others(21): Show | 24 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.719-89_719-88delTT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 17692233 | |||||
| chrX:17692899
|
A | G | 85 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(82): Show | 85 | HG00609.hp1 HG00639.hp2 HG01069.hp1 others(82): Show |
intron_variant | MODIFIER | c.852+431A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17692899 | ||||||
| chrX:17693406
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.852+938G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17693406 | ||||||
| chrX:17693596
|
C | T | 3 | a0001c0001t0012g0044a0004c0005t0010g0086a0008c0010t0003g0158 | 3 | HG02723.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.852+1128C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17693596 | ||||||
| chrX:17693736
|
G | A | 3 | a0001c0001t0002g0116a0001c0001t0009g0122a0013c0016t0002g0119 | 3 | HG02615.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.852+1268G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17693736 | ||||||
| chrX:17694125
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0009c0011t0002g0147 | 3 | HG02257.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.852+1657C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17694125 | ||||||
| chrX:17694481
|
G | C | 51 | a0001c0001t0001g0067a0001c0001t0001g0094a0001c0001t0001g0095others(48): Show | 51 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.852+2013G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17694481 | ||||||
| chrX:17694931
|
T | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852+2463T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17694931 | ||||||
| chrX:17695079
|
T | A | 2 | a0001c0001t0007g0073a0001c0001t0007g0102 | 2 | NA18955.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.852+2611T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17695079 | ||||||
| chrX:17695100
|
C | G | 1 | a0001c0001t0012g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.852+2632C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17695100 | ||||||
| chrX:17695474
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.852+3006G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17695474 | ||||||
| chrX:17695927
|
TA | T | 1 | a0002c0002t0001g0152 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.852+3474delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17695927 | |||||
| chrX:17695941
|
A | AG | 1 | a0002c0002t0001g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.852+3473_852+3474i others(3): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17695941 | ||||||
| chrX:17695941
|
AAG | A | 1 | a0006c0008t0008g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.852+3474_852+3475d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17695941 | ||||||
| chrX:17695942
|
A | AG | 5 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0052others(2): Show | 5 | HG02055.hp1 NA18986.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+3483dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17695942 | |||||
| chrX:17695942
|
A | G | 3 | a0002c0002t0001g0018a0002c0002t0001g0123a0002c0015t0001g0046 | 3 | HG00639.hp1 HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.852+3474A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17695942 | ||||||
| chrX:17695942
|
AG | A | 34 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0043others(31): Show | 34 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.852+3483delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17695942 | |||||
| chrX:17695949
|
G | A | 1 | a0002c0002t0001g0076 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.852+3481G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17695949 | ||||||
| chrX:17695951
|
G | T | 1 | a0002c0002t0001g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.852+3483G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17695951 | ||||||
| chrX:17695983
|
C | G | 1 | a0001c0003t0002g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.852+3515C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17695983 | ||||||
| chrX:17696221
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852+3753C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17696221 | ||||||
| chrX:17696344
|
G | A | 1 | a0001c0001t0004g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.852+3876G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17696344 | ||||||
| chrX:17696417
|
T | G | 161 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(158): Show | 161 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.852+3949T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17696417 | ||||||
| chrX:17696491
|
G | C | 1 | a0001c0001t0012g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.852+4023G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17696491 | ||||||
| chrX:17697106
|
C | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0124a0001c0001t0013g0059 | 3 | HG01943.hp1 HG02135.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.852+4638C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17697106 | ||||||
| chrX:17697209
|
AT | A | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.852+4744delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17697209 | |||||
| chrX:17697444
|
G | A | 30 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0043others(27): Show | 30 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.852+4976G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17697444 | ||||||
| chrX:17697771
|
A | C | 2 | a0001c0001t0009g0122a0001c0001t0009g0125 | 2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.852+5303A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17697771 | ||||||
| chrX:17697844
|
T | C | 1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.852+5376T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17697844 | ||||||
| chrX:17697928
|
CA | C | 1 | a0002c0002t0001g0003 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.852+5474delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17697928 | |||||
| chrX:17698059
|
G | C | 1 | a0008c0010t0003g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.852+5591G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17698059 | ||||||
| chrX:17698071
|
A | G | 3 | a0001c0001t0005g0103a0001c0001t0005g0111a0005c0006t0005g0159 | 3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.852+5603A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17698071 | ||||||
| chrX:17698374
|
G | A | 31 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0043others(28): Show | 31 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.852+5906G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17698374 | ||||||
| chrX:17698584
|
T | C | 27 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0004others(24): Show | 27 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.852+6116T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17698584 | ||||||
| chrX:17699010
|
A | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0125 | 2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.852+6542A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17699010 | ||||||
| chrX:17699265
|
A | G | 1 | a0001c0003t0002g0101 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.852+6797A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17699265 | ||||||
| chrX:17699539
|
T | A | 1 | a0001c0001t0001g0050 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.852+7071T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17699539 | ||||||
| chrX:17699607
|
A | C | 1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.852+7139A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17699607 | ||||||
| chrX:17700272
|
G | A | 1 | a0002c0002t0001g0078 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.852+7804G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17700272 | ||||||
| chrX:17700441
|
C | CA | 3 | a0001c0001t0002g0121a0002c0002t0001g0033a0008c0010t0003g0158 | 3 | HG01192.hp1 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.852+7986dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17700441 | |||||
| chrX:17700507
|
G | T | 28 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0043others(25): Show | 28 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.852+8039G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17700507 | ||||||
| chrX:17700614
|
C | CT | 1 | a0002c0002t0001g0015 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.852+8147dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17700614 | |||||
| chrX:17700746
|
T | C | 61 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(58): Show | 61 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.852+8278T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17700746 | ||||||
| chrX:17701516
|
TA | T | 86 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(83): Show | 86 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.852+9054delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17701516 | |||||
| chrX:17702277
|
G | A | 1 | a0002c0002t0001g0138 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.852+9809G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17702277 | ||||||
| chrX:17702996
|
C | T | 1 | a0002c0002t0001g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.852+10528C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17702996 | ||||||
| chrX:17703082
|
A | AATGT | 3 | a0001c0001t0005g0103a0001c0001t0005g0111a0005c0006t0005g0159 | 3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.852+10615_852+1061 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17703082 | |||||
| chrX:17703721
|
T | G | 5 | a0001c0001t0002g0002a0001c0001t0002g0106a0001c0001t0002g0107others(2): Show | 5 | HG02258.hp1 HG02293.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+11253T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17703721 | ||||||
| chrX:17704278
|
TA | T | 1 | a0001c0001t0007g0102 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.852+11818delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17704278 | |||||
| chrX:17704376
|
C | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.852+11908C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17704376 | ||||||
| chrX:17704540
|
C | T | 42 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(39): Show | 42 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.852+12072C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17704540 | ||||||
| chrX:17705440
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.852+12972T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17705440 | ||||||
| chrX:17705794
|
C | A | 1 | a0001c0001t0002g0110 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.852+13326C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17705794 | ||||||
| chrX:17706024
|
C | CA | 1 | a0002c0002t0006g0060 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.853-13311dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17706024 | |||||
| chrX:17706133
|
A | G | 5 | a0001c0001t0002g0002a0001c0001t0002g0106a0001c0001t0002g0107others(2): Show | 5 | HG02258.hp1 HG02293.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-13211A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17706133 | ||||||
| chrX:17706208
|
A | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0124a0001c0001t0013g0059 | 3 | HG01943.hp1 HG02135.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.853-13136A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17706208 | ||||||
| chrX:17706417
|
A | C | 3 | a0001c0001t0005g0103a0001c0001t0005g0111a0005c0006t0005g0159 | 3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.853-12927A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17706417 | ||||||
| chrX:17706490
|
A | AAC | 12 | a0002c0002t0001g0001a0002c0002t0001g0014a0002c0002t0001g0016others(9): Show | 12 | HG00408.hp2 HG00673.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.853-12820_853-1281 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17706490 | |||||
| chrX:17706490
|
A | AACAC | 1 | a0011c0013t0001g0039 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.853-12822_853-1281 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17706490 | |||||
| chrX:17706490
|
A | AC | 1 | a0002c0002t0001g0037 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.853-12854_853-1285 others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17706490 | ||||||
| chrX:17706490
|
AAC | A | 32 | a0001c0001t0001g0012a0001c0001t0001g0049a0001c0001t0001g0068others(29): Show | 32 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.853-12820_853-1281 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17706490 | |||||
| chrX:17706490
|
AACAC | A | 51 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0036others(48): Show | 51 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.853-12822_853-1281 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17706490 | |||||
| chrX:17706532
|
G | A | 1 | a0002c0002t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.853-12812G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17706532 | ||||||
| chrX:17706711
|
C | T | 86 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(83): Show | 86 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.853-12633C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17706711 | ||||||
| chrX:17707759
|
GTACAAGA others(5): Show |
G | 87 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(84): Show | 87 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.853-11584_853-1157 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17707759 | ||||||
| chrX:17707903
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.853-11441G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17707903 | ||||||
| chrX:17708023
|
C | T | 39 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(36): Show | 39 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.853-11321C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17708023 | ||||||
| chrX:17708029
|
G | A | 27 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0043others(24): Show | 27 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.853-11315G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17708029 | ||||||
| chrX:17708418
|
C | A | 4 | a0004c0005t0003g0100a0004c0005t0003g0117a0004c0005t0003g0136others(1): Show | 4 | HG01071.hp2 HG02055.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-10926C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17708418 | ||||||
| chrX:17708985
|
T | C | 1 | a0004c0005t0003g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.853-10359T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17708985 | ||||||
| chrX:17709016
|
CT | C | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-10323delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17709016 | |||||
| chrX:17709288
|
T | G | 5 | a0001c0001t0002g0002a0001c0001t0002g0106a0001c0001t0002g0107others(2): Show | 5 | HG02258.hp1 HG02293.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-10056T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17709288 | ||||||
| chrX:17709290
|
T | C | 3 | a0001c0001t0001g0137a0001c0001t0002g0085a0006c0008t0001g0114 | 3 | HG02451.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.853-10054T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17709290 | ||||||
| chrX:17709500
|
TCAGTCAG others(4): Show |
T | 13 | a0001c0001t0001g0137a0001c0001t0002g0085a0001c0001t0002g0096others(10): Show | 13 | HG01243.hp1 HG01258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.853-9835_853-9825d others(13): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17709500 | |||||
| chrX:17709637
|
A | G | 57 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(54): Show | 57 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.853-9707A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17709637 | ||||||
| chrX:17709751
|
G | A | 1 | a0002c0002t0001g0032 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.853-9593G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17709751 | ||||||
| chrX:17709927
|
G | A | 1 | a0002c0002t0001g0008 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.853-9417G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17709927 | ||||||
| chrX:17709937
|
A | AG | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-9405dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17709937 | |||||
| chrX:17709967
|
AG | A | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-9374delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17709967 | |||||
| chrX:17710054
|
C | CT | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-9290_853-9289i others(3): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17710054 | ||||||
| chrX:17710263
|
T | C | 1 | a0001c0001t0005g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.853-9081T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17710263 | ||||||
| chrX:17710290
|
CT | C | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-9051delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17710290 | |||||
| chrX:17710451
|
TA | T | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-8888delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17710451 | |||||
| chrX:17710520
|
G | C | 3 | a0001c0001t0005g0103a0001c0001t0005g0111a0005c0006t0005g0159 | 3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.853-8824G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17710520 | ||||||
| chrX:17710562
|
T | TA | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-8781dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17710562 | |||||
| chrX:17710573
|
CA | C | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-8766delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17710573 | |||||
| chrX:17710773
|
A | AG | 1 | a0002c0002t0001g0011 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.853-8567dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17710773 | |||||
| chrX:17710773
|
AG | A | 44 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0026others(41): Show | 44 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.853-8567delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17710773 | |||||
| chrX:17710836
|
TTA | T | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-8507_853-8506d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17710836 | ||||||
| chrX:17710902
|
A | G | 65 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(62): Show | 65 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.853-8442A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17710902 | ||||||
| chrX:17710973
|
TC | T | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-8367delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17710973 | |||||
| chrX:17710980
|
C | A | 1 | a0004c0005t0003g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.853-8364C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17710980 | ||||||
| chrX:17711012
|
C | T | 1 | a0002c0002t0001g0031 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.853-8332C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17711012 | ||||||
| chrX:17711096
|
T | C | 5 | a0001c0001t0002g0002a0001c0001t0002g0106a0001c0001t0002g0107others(2): Show | 5 | HG02258.hp1 HG02293.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-8248T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17711096 | ||||||
| chrX:17711100
|
TC | T | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-8241delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17711100 | |||||
| chrX:17711357
|
TTC | T | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-7984_853-7983d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17711357 | |||||
| chrX:17711367
|
TG | T | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-7974delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17711367 | |||||
| chrX:17711424
|
CA | C | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-7916delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17711424 | |||||
| chrX:17711519
|
AT | A | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-7821delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17711519 | |||||
| chrX:17711539
|
A | AG | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-7805_853-7804i others(3): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17711539 | ||||||
| chrX:17711573
|
G | GGA | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-7760_853-7759d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17711573 | |||||
| chrX:17711621
|
C | T | 1 | a0001c0001t0012g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.853-7723C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17711621 | ||||||
| chrX:17711631
|
GA | G | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-7709delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17711631 | |||||
| chrX:17711675
|
G | GC | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-7669_853-7668i others(3): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17711675 | ||||||
| chrX:17711688
|
A | AC | 1 | a0006c0007t0002g0118 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.853-7652dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17711688 | |||||
| chrX:17711689
|
C | A | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-7655C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17711689 | ||||||
| chrX:17711740
|
CT | C | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-7600delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17711740 | |||||
| chrX:17711851
|
G | A | 2 | a0002c0002t0001g0065a0002c0002t0001g0148 | 2 | NA19012.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.853-7493G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17711851 | ||||||
| chrX:17711853
|
TG | T | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-7488delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17711853 | |||||
| chrX:17712243
|
T | TTG | 1 | a0008c0010t0003g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.853-7091_853-7090d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712243 | |||||
| chrX:17712243
|
T | TTGTG | 1 | a0001c0001t0012g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.853-7093_853-7090d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712243 | |||||
| chrX:17712253
|
G | GTA | 11 | a0001c0001t0001g0026a0001c0001t0001g0067a0001c0001t0001g0144others(8): Show | 11 | HG00621.hp1 HG00673.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.853-7054_853-7053d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | |||||
| chrX:17712253
|
G | GTATA | 8 | a0001c0001t0007g0073a0001c0001t0007g0102a0001c0001t0009g0122others(5): Show | 8 | HG01074.hp1 HG02027.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.853-7056_853-7053d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | |||||
| chrX:17712253
|
G | GTATATA | 11 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0001g0061others(8): Show | 11 | HG00609.hp1 HG00639.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.853-7058_853-7053d others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | |||||
| chrX:17712253
|
G | GTATATAT others(1): Show |
4 | a0001c0001t0001g0048a0001c0001t0002g0116a0001c0001t0009g0125others(1): Show | 4 | HG03209.hp1 HG03516.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-7060_853-7053d others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | |||||
| chrX:17712253
|
G | GTATATAT others(3): Show |
3 | a0001c0001t0001g0050a0001c0001t0002g0096a0013c0016t0002g0119 | 3 | HG02630.hp2 HG02723.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.853-7062_853-7053d others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | |||||
| chrX:17712253
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0004g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.853-7064_853-7053d others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | |||||
| chrX:17712253
|
G | GTATATAT others(7): Show |
3 | a0001c0001t0001g0070a0001c0001t0004g0069a0001c0001t0013g0059 | 3 | HG02698.hp1 NA18965.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.853-7066_853-7053d others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | |||||
| chrX:17712253
|
G | GTATATAT others(9): Show |
3 | a0001c0001t0001g0022a0001c0001t0001g0124a0001c0001t0004g0058 | 3 | HG01943.hp1 HG02135.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.853-7068_853-7053d others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | |||||
| chrX:17712253
|
G | GTATATAT others(11): Show |
1 | a0001c0001t0001g0083 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.853-7070_853-7053d others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | |||||
| chrX:17712253
|
G | GTGTATA | 2 | a0001c0001t0002g0099a0001c0001t0002g0143 | 2 | HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.853-7090_853-7089i others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | |||||
| chrX:17712253
|
GTA | G | 14 | a0001c0001t0001g0127a0001c0001t0001g0151a0001c0001t0002g0085others(11): Show | 14 | HG00140.hp1 HG00408.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.853-7054_853-7053d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | |||||
| chrX:17712253
|
GTATA | G | 5 | a0001c0001t0001g0009a0001c0001t0017g0154a0004c0005t0003g0100others(2): Show | 5 | HG01975.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-7056_853-7053d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | |||||
| chrX:17712253
|
GTATATA | G | 2 | a0002c0002t0001g0033a0002c0002t0001g0075 | 2 | HG01192.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.853-7058_853-7053d others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | |||||
| chrX:17712253
|
GTATATAT others(3): Show |
G | 22 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0004others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.853-7062_853-7053d others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | |||||
| chrX:17712255
|
A | G | 4 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0135others(1): Show | 4 | HG01952.hp1 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-7089A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712255 | ||||||
| chrX:17712257
|
A | G | 3 | a0004c0005t0003g0117a0004c0005t0003g0136a0012c0014t0003g0092 | 3 | HG01071.hp2 HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.853-7087A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712257 | ||||||
| chrX:17712259
|
A | G | 4 | a0001c0001t0017g0154a0004c0005t0003g0100a0004c0005t0010g0086others(1): Show | 4 | HG01975.hp1 HG02055.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-7085A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712259 | ||||||
| chrX:17712265
|
A | G | 22 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0004others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.853-7079A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712265 | ||||||
| chrX:17712265
|
AT | A | 1 | a0001c0003t0002g0142 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.853-7078delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712265 | ||||||
| chrX:17712267
|
A | G | 1 | a0005c0006t0001g0157 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.853-7077A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712267 | ||||||
| chrX:17712268
|
TATATATA others(19): Show |
T | 2 | a0001c0001t0001g0036a0001c0001t0001g0056 | 2 | NA18988.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.853-7074_853-7049d others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712268 | |||||
| chrX:17712278
|
TATATATA others(7): Show |
T | 1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.853-7064_853-7051d others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712278 | |||||
| chrX:17712288
|
T | C | 3 | a0001c0001t0017g0154a0004c0005t0010g0086a0004c0005t0010g0097 | 3 | HG01975.hp1 HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.853-7056T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712288 | ||||||
| chrX:17712288
|
TATAC | T | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.853-7054_853-7051d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712288 | |||||
| chrX:17712288
|
TATACAC | T | 1 | a0002c0002t0001g0011 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.853-7054_853-7049d others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712288 | |||||
| chrX:17712290
|
T | C | 19 | a0001c0001t0001g0127a0001c0001t0001g0135a0002c0002t0001g0003others(16): Show | 19 | HG00280.hp1 HG00408.hp2 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.853-7054T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712290 | ||||||
| chrX:17712290
|
T | TAC | 14 | a0001c0001t0001g0012a0001c0001t0001g0049a0001c0001t0001g0052others(11): Show | 14 | HG00642.hp1 HG01928.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.853-7034_853-7033d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712290 | |||||
| chrX:17712290
|
T | TATAC | 5 | a0001c0001t0001g0068a0002c0002t0001g0047a0002c0002t0001g0053others(2): Show | 5 | HG03130.hp1 HG04199.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-7053_853-7052i others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712290 | |||||
| chrX:17712290
|
T | TATATAC | 2 | a0002c0002t0001g0089a0002c0002t0001g0105 | 2 | HG02129.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.853-7053_853-7052i others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712290 | |||||
| chrX:17712290
|
T | TATATATA others(1): Show |
1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-7053_853-7052i others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712290 | |||||
| chrX:17712290
|
T | TATATATA others(7): Show |
1 | a0002c0002t0001g0017 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.853-7053_853-7052i others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712290 | |||||
| chrX:17712290
|
TACAC | T | 1 | a0002c0002t0001g0082 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.853-7036_853-7033d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712290 | |||||
| chrX:17712292
|
C | T | 3 | a0001c0001t0002g0116a0002c0002t0001g0072a0013c0016t0002g0119 | 3 | HG02630.hp2 HG03017.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.853-7052C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712292 | ||||||
| chrX:17712312
|
T | C | 1 | a0003c0004t0001g0132 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.853-7032T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712312 | ||||||
| chrX:17712361
|
T | TAC | 10 | a0001c0001t0001g0009a0001c0001t0001g0061a0001c0001t0001g0083others(7): Show | 10 | HG02040.hp1 HG03942.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.853-6951_853-6950d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712361 | |||||
| chrX:17712361
|
T | TACAC | 8 | a0001c0001t0001g0050a0001c0001t0001g0090a0001c0003t0002g0019others(5): Show | 8 | HG01258.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-6953_853-6950d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712361 | |||||
| chrX:17712361
|
TAC | T | 2 | a0002c0002t0001g0040a0009c0011t0002g0147 | 2 | HG01167.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.853-6951_853-6950d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712361 | |||||
| chrX:17712361
|
TACAC | T | 2 | a0002c0002t0001g0017a0002c0002t0001g0077 | 2 | HG02293.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.853-6953_853-6950d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712361 | |||||
| chrX:17712371
|
C | G | 2 | a0001c0001t0002g0093a0001c0001t0002g0126 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.853-6973C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712371 | ||||||
| chrX:17712377
|
C | CACACACA | 1 | a0002c0002t0001g0062 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.853-6966_853-6960d others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712377 | |||||
| chrX:17712391
|
C | CAT | 18 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0043others(15): Show | 18 | HG01106.hp1 HG01109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.853-6952_853-6951i others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712391 | |||||
| chrX:17712393
|
C | CACACACA others(1): Show |
1 | a0004c0005t0010g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.853-6950_853-6949i others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712393 | |||||
| chrX:17712393
|
C | CACACAT | 2 | a0001c0001t0002g0164a0004c0005t0003g0100 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.853-6950_853-6949i others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712393 | |||||
| chrX:17712393
|
C | CACAT | 6 | a0001c0001t0017g0154a0004c0005t0003g0117a0004c0005t0003g0136others(3): Show | 6 | HG01071.hp2 HG01975.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-6950_853-6949i others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712393 | |||||
| chrX:17712393
|
C | CAT | 5 | a0001c0001t0007g0073a0001c0001t0007g0102a0002c0002t0001g0025others(2): Show | 5 | HG02056.hp1 HG04199.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-6932_853-6931d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712393 | |||||
| chrX:17712393
|
C | CATAT | 4 | a0001c0001t0002g0004a0001c0001t0002g0093a0001c0001t0002g0126others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-6934_853-6931d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712393 | |||||
| chrX:17712393
|
C | T | 22 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0043others(19): Show | 22 | HG01106.hp1 HG01109.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.853-6951C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712393 | ||||||
| chrX:17712393
|
CAT | C | 1 | a0001c0001t0002g0085 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.853-6932_853-6931d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712393 | |||||
| chrX:17712395
|
T | C | 2 | a0001c0001t0001g0068a0011c0013t0001g0039 | 2 | HG03130.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.853-6949T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712395 | ||||||
| chrX:17712550
|
G | T | 30 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0004others(27): Show | 30 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.853-6794G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712550 | ||||||
| chrX:17713052
|
A | G | 2 | a0001c0001t0012g0044a0009c0011t0002g0147 | 2 | HG02257.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.853-6292A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17713052 | ||||||
| chrX:17713091
|
ATTTTGAG others(13): Show |
A | 1 | a0002c0002t0001g0028 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.853-6252_853-6233d others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17713091 | ||||||
| chrX:17713263
|
T | C | 1 | a0002c0002t0001g0033 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.853-6081T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17713263 | ||||||
| chrX:17713612
|
A | G | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.853-5732A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17713612 | ||||||
| chrX:17713840
|
C | T | 1 | a0001c0001t0009g0125 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.853-5504C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17713840 | ||||||
| chrX:17714149
|
C | CT | 3 | a0001c0001t0001g0098a0002c0002t0001g0037a0002c0002t0006g0060 | 3 | NA18940.hp1 NA18985.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.853-5181dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17714149 | |||||
| chrX:17714149
|
CT | C | 1 | a0002c0002t0001g0139 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.853-5181delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17714149 | |||||
| chrX:17714182
|
A | T | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.853-5162A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17714182 | ||||||
| chrX:17714280
|
G | A | 2 | a0002c0002t0001g0008a0002c0002t0001g0040 | 2 | HG01167.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.853-5064G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17714280 | ||||||
| chrX:17714576
|
T | C | 4 | a0003c0004t0001g0013a0003c0004t0001g0132a0003c0004t0001g0149others(1): Show | 4 | HG01952.hp1 HG02300.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-4768T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17714576 | ||||||
| chrX:17715226
|
G | C | 8 | a0001c0001t0017g0154a0004c0005t0003g0100a0004c0005t0003g0117others(5): Show | 8 | HG01071.hp2 HG01975.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-4118G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17715226 | ||||||
| chrX:17715321
|
T | C | 3 | a0001c0001t0002g0093a0001c0001t0002g0126a0001c0001t0002g0146 | 3 | HG01069.hp1 HG01071.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.853-4023T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17715321 | ||||||
| chrX:17716785
|
A | G | 3 | a0001c0001t0005g0103a0001c0001t0005g0111a0005c0006t0005g0159 | 3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.853-2559A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17716785 | ||||||
| chrX:17716960
|
C | CT | 1 | a0004c0005t0010g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.853-2383dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17716960 | |||||
| chrX:17716962
|
C | CT | 11 | a0001c0001t0001g0090a0001c0001t0001g0144a0001c0001t0007g0073others(8): Show | 11 | HG00642.hp1 HG02074.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.853-2365dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17716962 | |||||
| chrX:17716962
|
C | T | 26 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0043others(23): Show | 26 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.853-2382C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17716962 | ||||||
| chrX:17717074
|
TCTC | T | 6 | a0002c0002t0001g0024a0003c0004t0001g0055a0003c0004t0001g0066others(3): Show | 6 | HG01952.hp1 NA18948.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-2267_853-2265d others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17717074 | |||||
| chrX:17717282
|
T | C | 1 | a0008c0010t0003g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.853-2062T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17717282 | ||||||
| chrX:17717465
|
T | C | 4 | a0001c0001t0002g0116a0001c0001t0012g0044a0009c0011t0002g0147others(1): Show | 4 | HG02257.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-1879T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17717465 | ||||||
| chrX:17717872
|
C | CAAAT | 1 | a0002c0002t0001g0047 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.853-1456_853-1453d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17717872 | |||||
| chrX:17718068
|
T | C | 3 | a0001c0001t0005g0103a0001c0001t0005g0111a0005c0006t0005g0159 | 3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.853-1276T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17718068 | ||||||
| chrX:17718106
|
T | C | 1 | a0002c0002t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.853-1238T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17718106 | ||||||
| chrX:17718209
|
G | GC | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.853-1131dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17718209 | |||||
| chrX:17718319
|
G | A | 1 | a0001c0003t0002g0101 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.853-1025G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17718319 | ||||||
| chrX:17718346
|
A | AG | 4 | a0001c0001t0001g0050a0002c0002t0001g0033a0002c0002t0001g0141others(1): Show | 4 | HG00642.hp1 HG01192.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-995dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17718346 | |||||
| chrX:17718350
|
T | G | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.853-994T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17718350 | ||||||
| chrX:17718427
|
GAAGA | G | 25 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0043others(22): Show | 25 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.853-913_853-910del others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17718427 | |||||
| chrX:17718645
|
AGAAG | A | 1 | a0001c0001t0001g0151 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.853-689_853-686del others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17718645 | |||||
| chrX:17718736
|
G | A | 1 | a0002c0002t0001g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.853-608G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17718736 | ||||||
| chrX:17718917
|
G | GGAA | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.853-423_853-421dup others(3): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17718917 | |||||
| chrX:17718953
|
AG | A | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.853-388delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17718953 | |||||
| chrX:17719136
|
A | AAAGG | 3 | a0001c0001t0005g0103a0001c0001t0005g0111a0005c0006t0005g0159 | 3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.853-201_853-198dup others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17719136 | |||||
| chrX:17719150
|
TAAG | T | 1 | a0001c0003t0002g0155 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.853-193_853-191del others(3): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17719150 | ||||||
| chrX:17719160
|
GA | G | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.853-182delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17719160 | |||||
| chrX:17719605
|
TC | T | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.915+204delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 17719605 | |||||
| chrX:17719648
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.915+242C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 4/8 | chrX | 17719648 | ||||||
| chrX:17719978
|
T | TTC | 2 | a0001c0001t0002g0116a0013c0016t0002g0119 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.915+590_915+591dup others(2): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 17719978 | |||||
| chrX:17720364
|
AT | A | 1 | a0001c0001t0001g0104 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.915+966delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 17720364 | |||||
| chrX:17720425
|
C | A | 3 | a0001c0001t0001g0137a0001c0001t0002g0085a0006c0008t0001g0114 | 3 | HG02451.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.916-1016C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 4/8 | chrX | 17720425 | ||||||
| chrX:17720437
|
A | G | 2 | a0002c0002t0001g0023a0002c0002t0001g0054 | 2 | HG02027.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.916-1004A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 4/8 | chrX | 17720437 | ||||||
| chrX:17720662
|
A | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0056 | 2 | NA18988.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.916-779A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 4/8 | chrX | 17720662 | ||||||
| chrX:17721381
|
C | CT | 1 | a0002c0002t0001g0011 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.916-58dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 17721381 | |||||
| chrX:17722166
|
T | TC | 1 | a0002c0002t0001g0011 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1108+534dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17722166 | |||||
| chrX:17722243
|
C | T | 1 | a0002c0002t0001g0025 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1108+610C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17722243 | ||||||
| chrX:17723028
|
G | A | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1109-1271G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723028 | ||||||
| chrX:17723203
|
C | T | 2 | a0001c0001t0002g0116a0013c0016t0002g0119 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1109-1096C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723203 | ||||||
| chrX:17723572
|
T | C | 3 | a0001c0001t0005g0103a0001c0001t0005g0111a0005c0006t0005g0159 | 3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1109-727T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723572 | ||||||
| chrX:17723726
|
G | GGT | 10 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0049others(7): Show | 10 | HG01243.hp1 HG01975.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.1109-529_1109-528d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | |||||
| chrX:17723726
|
G | GGTGT | 9 | a0001c0001t0001g0133a0001c0001t0002g0143a0002c0002t0001g0016others(6): Show | 9 | HG00280.hp1 HG01975.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1109-531_1109-528d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | |||||
| chrX:17723726
|
G | GGTGTGT | 12 | a0001c0001t0001g0151a0001c0003t0002g0128a0002c0002t0001g0010others(9): Show | 12 | HG00408.hp1 HG01256.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1109-533_1109-528d others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | |||||
| chrX:17723726
|
G | GGTGTGTG others(1): Show |
20 | a0001c0001t0001g0009a0001c0001t0001g0068a0001c0001t0001g0094others(17): Show | 20 | HG00642.hp1 HG01099.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1109-535_1109-528d others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | |||||
| chrX:17723726
|
G | GGTGTGTG others(3): Show |
20 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0041others(17): Show | 20 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1109-537_1109-528d others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | |||||
| chrX:17723726
|
G | GGTGTGTG others(5): Show |
11 | a0001c0001t0001g0022a0001c0001t0001g0061a0001c0001t0001g0083others(8): Show | 11 | HG02040.hp1 HG02135.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1109-539_1109-528d others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | |||||
| chrX:17723726
|
G | GGTGTGTG others(7): Show |
7 | a0001c0001t0001g0038a0001c0001t0001g0048a0001c0001t0001g0050others(4): Show | 7 | HG00639.hp2 HG01515.hp1 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.1109-541_1109-528d others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | |||||
| chrX:17723726
|
G | GGTGTGTG others(9): Show |
8 | a0001c0001t0001g0057a0001c0001t0001g0081a0001c0001t0001g0153others(5): Show | 8 | HG00609.hp1 HG00673.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1109-543_1109-528d others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | |||||
| chrX:17723726
|
G | GGTGTGTG others(11): Show |
4 | a0001c0001t0001g0070a0001c0003t0002g0019a0002c0002t0001g0065others(1): Show | 4 | HG01258.hp1 HG02698.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1109-545_1109-528d others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | |||||
| chrX:17723726
|
G | GGTGTGTG others(13): Show |
1 | a0002c0002t0006g0060 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1109-547_1109-528d others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | |||||
| chrX:17723726
|
G | GTGTGTGT others(8): Show |
1 | a0001c0001t0001g0134 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1109-573_1109-572i others(17): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723726 | ||||||
| chrX:17723726
|
GGT | G | 4 | a0001c0001t0001g0135a0002c0002t0001g0054a0008c0010t0003g0158others(1): Show | 4 | HG02056.hp1 HG02723.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1109-529_1109-528d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | |||||
| chrX:17723741
|
G | GTGTGTGT others(6): Show |
1 | a0003c0004t0001g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1109-557_1109-545d others(15): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723741 | |||||
| chrX:17723741
|
G | GTGTGTGT others(11): Show |
1 | a0001c0001t0005g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1109-541_1109-540i others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723741 | |||||
| chrX:17723762
|
TGTGTGTG others(7): Show |
T | 1 | a0001c0001t0002g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1109-535_1109-522d others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723762 | |||||
| chrX:17723763
|
G | A | 2 | a0001c0001t0005g0103a0005c0006t0005g0159 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1109-536G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723763 | ||||||
| chrX:17723764
|
TGTGTGTG others(5): Show |
T | 1 | a0013c0016t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1109-533_1109-522d others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723764 | |||||
| chrX:17723768
|
T | TGCGC | 1 | a0004c0005t0010g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1109-530_1109-529i others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723768 | |||||
| chrX:17723770
|
T | C | 3 | a0002c0002t0001g0011a0004c0005t0010g0086a0008c0010t0003g0158 | 3 | HG02723.hp2 HG02965.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1109-529T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723770 | ||||||
| chrX:17723770
|
T | TGC | 3 | a0001c0001t0002g0121a0004c0005t0003g0100a0004c0005t0010g0097 | 3 | HG02055.hp1 HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1109-521_1109-520d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGCGC | 1 | a0001c0001t0002g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1109-523_1109-520d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGCGCGC | 2 | a0001c0001t0002g0120a0001c0001t0006g0112 | 2 | HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1109-525_1109-520d others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGTGC | 5 | a0001c0001t0002g0164a0002c0002t0001g0001a0002c0002t0016g0005others(2): Show | 5 | HG00621.hp1 HG01106.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1109-528_1109-527i others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGTGCGC | 5 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1109-528_1109-527i others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGTGCGCG others(3): Show |
1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1109-528_1109-527i others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGTGTGC | 5 | a0001c0001t0002g0093a0001c0001t0002g0126a0001c0001t0002g0146others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1109-528_1109-527i others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGTGTGCG others(1): Show |
2 | a0006c0008t0001g0114a0009c0011t0002g0147 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1109-528_1109-527i others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGTGTGCG others(3): Show |
1 | a0002c0002t0001g0033 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1109-528_1109-527i others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGTGTGTG others(1): Show |
4 | a0001c0001t0012g0044a0001c0003t0002g0101a0002c0002t0001g0075others(1): Show | 4 | HG02922.hp2 HG03453.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1109-528_1109-527i others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGTGTGTG others(3): Show |
1 | a0002c0002t0001g0076 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1109-528_1109-527i others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGTGTGTG others(3): Show |
1 | a0006c0007t0002g0118 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1109-528_1109-527i others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGTGTGTG others(7): Show |
1 | a0002c0002t0001g0080 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1109-528_1109-527i others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGTGTGTG others(7): Show |
1 | a0001c0001t0002g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1109-528_1109-527i others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGTGTGTG others(9): Show |
1 | a0001c0001t0004g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1109-528_1109-527i others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGTGTGTG others(7): Show |
1 | a0002c0002t0001g0035 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1109-528_1109-527i others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGTGTGTG others(9): Show |
1 | a0001c0001t0009g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1109-528_1109-527i others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGTGTGTG others(9): Show |
2 | a0001c0001t0001g0140a0001c0001t0009g0125 | 2 | HG01934.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1109-528_1109-527i others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGTGTGTG others(11): Show |
2 | a0001c0001t0001g0144a0006c0007t0002g0115 | 2 | HG02809.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1109-528_1109-527i others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGTGTGTG others(13): Show |
1 | a0001c0001t0001g0129 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1109-528_1109-527i others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGTGTGTG others(19): Show |
1 | a0005c0006t0005g0159 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1109-528_1109-527i others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723770
|
T | TGTGTGTG others(19): Show |
1 | a0001c0001t0005g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1109-528_1109-527i others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | |||||
| chrX:17723772
|
C | T | 15 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0049others(12): Show | 15 | HG01243.hp1 HG02071.hp1 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.1109-527C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723772 | ||||||
| chrX:17723773
|
G | A | 2 | a0001c0001t0005g0103a0005c0006t0005g0159 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1109-526G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723773 | ||||||
| chrX:17723773
|
G | GCGCA | 1 | a0001c0001t0005g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1109-523_1109-522i others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723773 | |||||
| chrX:17723776
|
C | CT | 1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1109-523_1109-522i others(3): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723776 | ||||||
| chrX:17723777
|
G | GC | 1 | a0001c0001t0004g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1109-521dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723777 | |||||
| chrX:17723777
|
G | GCGA | 1 | a0002c0002t0001g0062 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1109-520_1109-519i others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723777 | |||||
| chrX:17723779
|
G | GC | 1 | a0002c0002t0001g0011 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1109-520_1109-519i others(3): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723779 | ||||||
| chrX:17723779
|
G | GCGCGCGC | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1109-520_1109-519i others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723779 | ||||||
| chrX:17723780
|
T | A | 2 | a0001c0001t0002g0002a0002c0002t0001g0011 | 2 | HG02293.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1109-519T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723780 | ||||||
| chrX:17723780
|
T | C | 162 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(159): Show | 162 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1109-519T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723780 | ||||||
| chrX:17723798
|
A | G | 33 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0004others(30): Show | 33 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1109-501A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723798 | ||||||
| chrX:17724211
|
C | T | 1 | a0002c0002t0001g0089 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1109-88C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17724211 | ||||||
| chrX:17724709
|
A | C | 1 | a0009c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1240+279A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 6/8 | chrX | 17724709 | ||||||
| chrX:17724776
|
T | C | 1 | a0001c0001t0001g0026 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1240+346T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 6/8 | chrX | 17724776 | ||||||
| chrX:17725234
|
G | GA | 1 | a0002c0002t0006g0060 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1241-102dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 17725234 | |||||
| chrX:17725234
|
GA | G | 12 | a0001c0001t0001g0038a0001c0001t0001g0067a0001c0001t0001g0081others(9): Show | 12 | HG00639.hp2 HG02132.hp1 HG03579.hp1 others(9): Show |
intron_variant | MODIFIER | c.1241-102delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 17725234 | |||||
| chrX:17728549
|
C | CTGTT | 37 | a0001c0001t0001g0137a0001c0001t0002g0002a0001c0001t0002g0004others(34): Show | 37 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.4223-75_4223-72dup others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 17728549 | |||||
| chrX:17728549
|
C | CTGTTTGT others(1): Show |
3 | a0005c0006t0008g0161a0006c0008t0008g0113a0007c0009t0002g0160 | 3 | HG02145.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4223-79_4223-72dup others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 17728549 | |||||
| chrX:17728549
|
CTGTT | C | 2 | a0001c0003t0002g0128a0004c0005t0003g0100 | 2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.4223-75_4223-72del others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 17728549 | |||||
| chrX:17729431
|
G | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0125 | 2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4349+656G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | chrX | 17729431 | ||||||
| chrX:17729925
|
C | T | 1 | a0002c0002t0001g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4349+1150C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | chrX | 17729925 | ||||||
| chrX:17730091
|
T | C | 3 | a0001c0001t0005g0103a0001c0001t0005g0111a0005c0006t0005g0159 | 3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4349+1316T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | chrX | 17730091 | ||||||
| chrX:17730551
|
A | G | 3 | a0001c0001t0005g0103a0001c0001t0005g0111a0005c0006t0005g0159 | 3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4350-1307A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | chrX | 17730551 | ||||||
| chrX:17730732
|
C | T | 1 | a0002c0002t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4350-1126C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | chrX | 17730732 | ||||||
| chrX:17731020
|
T | C | 3 | a0001c0001t0005g0103a0001c0001t0005g0111a0005c0006t0005g0159 | 3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4350-838T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | chrX | 17731020 | ||||||
| chrX:17731224
|
C | CT | 4 | a0001c0001t0005g0111a0001c0001t0009g0122a0001c0001t0009g0125others(1): Show | 4 | HG02615.hp2 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.4350-606dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 17731224 | |||||
| chrX:17731224
|
CT | C | 114 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(111): Show | 114 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.4350-606delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 17731224 | |||||
| chrX:17731224
|
CTT | C | 18 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0002g0085others(15): Show | 18 | HG01243.hp1 HG01258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.4350-607_4350-606d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 17731224 | |||||
| chrX:17731224
|
CTTTTTTT others(1): Show |
C | 1 | a0001c0001t0002g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4350-613_4350-606d others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 17731224 | |||||
| chrX:17731287
|
G | C | 4 | a0002c0002t0001g0087a0002c0002t0001g0088a0002c0002t0001g0089others(1): Show | 4 | HG02074.hp1 HG02129.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.4350-571G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | chrX | 17731287 | ||||||
| chrX:17731510
|
T | C | 17 | a0001c0001t0001g0137a0001c0001t0002g0004a0001c0001t0002g0043others(14): Show | 17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.4350-348T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | chrX | 17731510 | ||||||
| chrX:17731783
|
T | C | 3 | a0001c0001t0005g0103a0001c0001t0005g0111a0005c0006t0005g0159 | 3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4350-75T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | chrX | 17731783 |