Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 412 |
|---|---|
| ensemblid | ENSG00000101846.9 |
| hgncid | 11425 |
| symbol | STS |
| name | steroid sulfatase |
| refseq_nuc | NM_001320752.2 |
| refseq_prot | NP_001307681.2 |
| ensembl_nuc | ENST00000674429.1 |
| ensembl_prot | ENSP00000501534.1 |
| mane_status | MANE Select |
| chr | chrX |
| start | 7147712 |
| end | 7354641 |
| strand | + |
| ver | v1.2 |
| region | chrX:7147712-7354641 |
| region5000 | chrX:7142712-7359641 |
| regionname0 | STS_chrX_7147712_7354641 |
| regionname5000 | STS_chrX_7142712_7359641 |
| 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 | 1/1 | 578 | 223 | 50 | 44 | 95 | 11 | 21 | 78 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0002 | 0/0 | 578 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0003 | 0/0 | 578 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0004 | 0/0 | 578 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0005 | 0/0 | 578 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0006 | 0/0 | 578 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0007 | 0/0 | 578 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| 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 | 1/1 | 1737 | 221 | 49 | 44 | 94 | 11 | 21 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| c0002 | 0/0 | 1737 | 2 | 2 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| c0003 | 0/0 | 1737 | 2 | 0 | 0 | 2 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| c0004 | 0/0 | 1737 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| c0005 | 0/0 | 1737 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| c0006 | 0/0 | 1737 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| c0007 | 0/0 | 1737 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| c0008 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| c0009 | 0/0 | 1737 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| 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 | 4886 | 64 | 16 | 10 | 29 | 2 | 7 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0002 | 0/0 | 4886 | 50 | 13 | 10 | 17 | 3 | 7 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0003 | 0/0 | 4886 | 44 | 2 | 15 | 23 | 2 | 2 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0004 | 0/0 | 4887 | 15 | 0 | 0 | 15 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0005 | 0/0 | 4886 | 9 | 9 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0006 | 0/1 | 4886 | 5 | 0 | 1 | 0 | 2 | 1 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0007 | 1/0 | 4886 | 4 | 0 | 0 | 0 | 2 | 1 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0008 | 0/0 | 4886 | 2 | 0 | 2 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0009 | 0/0 | 4885 | 2 | 0 | 1 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0010 | 0/0 | 4886 | 2 | 2 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0011 | 0/0 | 4887 | 2 | 1 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0012 | 0/0 | 4886 | 2 | 0 | 2 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0013 | 0/0 | 4885 | 2 | 0 | 1 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0014 | 0/0 | 4887 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0015 | 0/0 | 4887 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0016 | 0/0 | 4886 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0017 | 0/0 | 4886 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0018 | 0/0 | 4886 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0019 | 0/0 | 4886 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0020 | 0/0 | 4885 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0021 | 0/0 | 4889 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0022 | 0/0 | 4886 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0023 | 0/0 | 4887 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0024 | 0/0 | 4886 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0025 | 0/0 | 4885 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0026 | 0/0 | 4886 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0027 | 0/0 | 4886 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0028 | 0/0 | 4886 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0029 | 0/0 | 4886 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0030 | 0/0 | 4886 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0031 | 0/0 | 4886 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0032 | 0/0 | 4886 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0033 | 0/0 | 4882 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0034 | 0/0 | 4882 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0035 | 0/0 | 4885 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0036 | 0/0 | 4886 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0037 | 0/0 | 4886 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0038 | 0/0 | 4886 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0039 | 0/0 | 4889 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0040 | 0/0 | 4886 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| t0041 | 0/0 | 4889 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| 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 | 1/1 | 1737 | 221 | 49 | 44 | 94 | 11 | 21 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0006 | 0/0 | 1737 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0008 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0002c0002 | 0/0 | 1737 | 2 | 2 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0003c0003 | 0/0 | 1737 | 2 | 0 | 0 | 2 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0004c0009 | 0/0 | 1737 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0005c0005 | 0/0 | 1737 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0006c0007 | 0/0 | 1737 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0007c0004 | 0/0 | 1737 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6622 | 63 | 16 | 10 | 29 | 2 | 6 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0002 | 0/0 | 6622 | 49 | 13 | 9 | 17 | 3 | 7 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0003 | 0/0 | 6622 | 40 | 2 | 14 | 20 | 2 | 2 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0004 | 0/0 | 6623 | 14 | 0 | 0 | 14 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0005 | 0/0 | 6622 | 8 | 8 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0006 | 0/1 | 6622 | 5 | 0 | 1 | 0 | 2 | 1 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0007 | 1/0 | 6622 | 4 | 0 | 0 | 0 | 2 | 1 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0008 | 0/0 | 6622 | 2 | 0 | 2 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0009 | 0/0 | 6621 | 2 | 0 | 1 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0010 | 0/0 | 6622 | 2 | 2 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0011 | 0/0 | 6623 | 2 | 1 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0012 | 0/0 | 6622 | 2 | 0 | 2 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0013 | 0/0 | 6621 | 2 | 0 | 1 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0014 | 0/0 | 6623 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0015 | 0/0 | 6623 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0016 | 0/0 | 6622 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0017 | 0/0 | 6622 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0018 | 0/0 | 6622 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0019 | 0/0 | 6622 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0021 | 0/0 | 6625 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0022 | 0/0 | 6622 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0023 | 0/0 | 6623 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0024 | 0/0 | 6622 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0025 | 0/0 | 6621 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0026 | 0/0 | 6622 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0028 | 0/0 | 6622 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0029 | 0/0 | 6622 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0030 | 0/0 | 6622 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0031 | 0/0 | 6622 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0032 | 0/0 | 6622 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0033 | 0/0 | 6618 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0034 | 0/0 | 6618 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0035 | 0/0 | 6621 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0036 | 0/0 | 6622 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0037 | 0/0 | 6622 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0038 | 0/0 | 6622 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0039 | 0/0 | 6625 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0040 | 0/0 | 6622 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0001t0041 | 0/0 | 6625 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0006t0004 | 0/0 | 6623 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0001c0008t0005 | 0/0 | 6622 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0002c0002t0020 | 0/0 | 6621 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0002c0002t0027 | 0/0 | 6622 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0003c0003t0003 | 0/0 | 6622 | 2 | 0 | 0 | 2 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0004c0009t0002 | 0/0 | 6622 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0005c0005t0003 | 0/0 | 6622 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0006c0007t0001 | 0/0 | 6622 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| a0007c0004t0003 | 0/0 | 6622 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | copy fasta | chrX | 7142712 | 7359641 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0006g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0006g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0006g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0007g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0007g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0007g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0007g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0008g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0008g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0009g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0009g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0010g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0010g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0011g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0011g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0012g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0012g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0013g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0013g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0014g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0015g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0016g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0017g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0018g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0019g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0021g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0022g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0023g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0024g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0025g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0026g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0028g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0029g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0030g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0031g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0032g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0033g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0034g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0035g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0036g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0037g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0038g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0039g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0040g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0001t0041g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0006t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0001c0008t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0002c0002t0020g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0002c0002t0027g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0003c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0003c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0004c0009t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0005c0005t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0006c0007t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| a0007c0004t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | GBR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0187 | EUR | GBR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0155 | EUR | GBR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0153 | EUR | FIN | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0197 | EUR | FIN | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG00323 | hp2 | a0001 | c0001 | t0007 | g0154 | EUR | FIN | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0077 | EAS | CHS | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG00639 | hp1 | a0001 | c0001 | t0022 | g0065 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0158 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | CHS | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0140 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01069 | hp1 | a0001 | c0001 | t0012 | g0028 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01071 | hp1 | a0001 | c0001 | t0012 | g0029 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0117 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01074 | hp1 | a0001 | c0001 | t0023 | g0228 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01106 | hp1 | a0004 | c0009 | t0002 | g0225 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01168 | hp1 | a0001 | c0001 | t0008 | g0178 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01169 | hp1 | a0001 | c0001 | t0008 | g0177 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01169 | hp2 | a0001 | c0001 | t0009 | g0120 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | CLM | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01256 | hp1 | a0001 | c0001 | t0013 | g0051 | AMR | CLM | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0132 | AMR | CLM | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0131 | AMR | CLM | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | CLM | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01358 | hp1 | a0005 | c0005 | t0003 | g0164 | AMR | CLM | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | CLM | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0214 | EUR | IBS | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0168 | EUR | IBS | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | PEL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0113 | AMR | PEL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02004 | hp1 | a0001 | c0001 | t0016 | g0159 | AMR | PEL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02004 | hp2 | a0001 | c0001 | t0028 | g0195 | AMR | PEL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | KHV | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | KHV | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02055 | hp1 | a0001 | c0001 | t0010 | g0100 | AFR | ACB | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02056 | hp1 | a0001 | c0001 | t0015 | g0102 | EAS | KHV | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02074 | hp1 | a0001 | c0001 | t0031 | g0018 | EAS | KHV | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | KHV | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02132 | hp1 | a0001 | c0001 | t0017 | g0121 | EAS | KHV | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0221 | AFR | ACB | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | ACB | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02257 | hp2 | a0002 | c0002 | t0020 | g0009 | AFR | ACB | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0226 | AFR | ACB | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | PEL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0222 | AFR | GWD | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0056 | AFR | GWD | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02698 | hp1 | a0001 | c0001 | t0033 | g0191 | SAS | PJL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0176 | SAS | PJL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02738 | hp1 | a0001 | c0001 | t0014 | g0216 | SAS | PJL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0223 | AFR | GWD | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | GWD | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | ESN | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ESN | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02970 | hp2 | a0001 | c0001 | t0032 | g0057 | AFR | ESN | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02976 | hp1 | a0001 | c0001 | t0035 | g0229 | AFR | ESN | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0162 | SAS | PJL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0041 | AFR | MSL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | ESN | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | ESN | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0138 | AFR | ESN | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03209 | hp1 | a0001 | c0001 | t0038 | g0219 | AFR | MSL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03453 | hp1 | a0001 | c0008 | t0005 | g0134 | AFR | MSL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03490 | hp1 | a0001 | c0001 | t0007 | g0126 | SAS | PJL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | ESN | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03516 | hp2 | a0001 | c0001 | t0037 | g0224 | AFR | ESN | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0145 | AFR | MSL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | STU | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03831 | hp2 | a0001 | c0001 | t0018 | g0141 | SAS | BEB | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | BEB | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | STU | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG04184 | hp1 | a0006 | c0007 | t0001 | g0039 | SAS | BEB | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0157 | SAS | BEB | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | STU | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | STU | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG04228 | hp1 | a0001 | c0001 | t0019 | g0103 | SAS | STU | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | CHB | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | CHB | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18952 | hp1 | a0001 | c0006 | t0004 | g0088 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18957 | hp1 | a0003 | c0003 | t0003 | g0147 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18965 | hp1 | a0001 | c0001 | t0009 | g0170 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18975 | hp1 | a0001 | c0001 | t0011 | g0026 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18990 | hp1 | a0001 | c0001 | t0029 | g0034 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19003 | hp1 | a0007 | c0004 | t0003 | g0150 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19007 | hp1 | a0001 | c0001 | t0034 | g0045 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19012 | hp1 | a0001 | c0001 | t0024 | g0211 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19043 | hp1 | a0001 | c0001 | t0026 | g0143 | AFR | LWK | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19057 | hp1 | a0001 | c0001 | t0025 | g0202 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19058 | hp1 | a0001 | c0001 | t0021 | g0096 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19060 | hp1 | a0003 | c0003 | t0003 | g0146 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19063 | hp1 | a0001 | c0001 | t0013 | g0033 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19077 | hp1 | a0001 | c0001 | t0030 | g0038 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19083 | hp1 | a0001 | c0001 | t0039 | g0079 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19089 | hp2 | a0001 | c0001 | t0041 | g0003 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | ASW | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA20129 | hp2 | a0002 | c0002 | t0027 | g0097 | AFR | ASW | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0166 | EUR | TSI | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0160 | EUR | TSI | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | GIH | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | CLM | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0109 | AMR | CLM | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0220 | AFR | ACB | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02109 | hp2 | a0001 | c0001 | t0036 | g0006 | AFR | ACB | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0218 | AFR | ACB | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | ACB | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| HG03471 | hp1 | a0001 | c0001 | t0040 | g0227 | AFR | MSL | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | USA | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | USA | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0006 | g0161 | REF | REF | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0165 | REF | REF | STS_chrX_7142712_7359641 | STS | chrX | 7142712 | 7359641 |
| 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:7257255
|
G | A | 1 | a0007 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.151G>A | p.Asp51Asn | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 4/11 | 656/6622 | 151/1737 | 51/578 | chrX | 7257255 | ||
| chrX:7259721
|
A | T | 1 | a0004 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.755A>T | p.Tyr252Phe | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/11 | 1260/6622 | 755/1737 | 252/578 | chrX | 7259721 | ||
| chrX:7276048
|
G | A | 1 | a0002 | 2 | HG02257.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.904G>A | p.Val302Ile | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/11 | 1409/6622 | 904/1737 | 302/578 | chrX | 7276048 | ||
| chrX:7325381
|
G | C | 1 | a0005 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.1124G>C | p.Gly375Ala | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/11 | 1629/6622 | 1124/1737 | 375/578 | chrX | 7325381 | ||
| chrX:7349935
|
G | A | 1 | a0003 | 2 | NA18957.hp1 NA19060.hp1 |
missense_variant | MODERATE | c.1411G>A | p.Val471Met | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 1916/6622 | 1411/1737 | 471/578 | chrX | 7349935 | ||
| chrX:7350061
|
G | A | 1 | a0006 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.1537G>A | p.Ala513Thr | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 2042/6622 | 1537/1737 | 513/578 | chrX | 7350061 |
| 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:7334016
|
G | A | 1 | a0001c0006 | 1 | NA18952.hp1 | synonymous_variant | LOW | c.1272G>A | p.Leu424Leu | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/11 | 1777/6622 | 1272/1737 | 424/578 | chrX | 7334016 | ||
| chrX:7350090
|
C | T | 1 | a0001c0008 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1566C>T | p.Leu522Leu | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 2071/6622 | 1566/1737 | 522/578 | chrX | 7350090 |
| 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:7147758
|
A | AG | 1 | a0001c0001t0041 | 1 | NA19089.hp2 | 5_prime_UTR_variant | MODIFIER | c.-456dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/11 | 105438 | INFO_REALIGN_3_PRIME | chrX | 7147758 | ||||
| chrX:7147823
|
G | T | 1 | a0001c0001t0040 | 1 | HG03471.hp1 | 5_prime_UTR_variant | MODIFIER | c.-394G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/11 | 105377 | chrX | 7147823 | |||||
| chrX:7147846
|
G | GC | 1 | a0001c0001t0041 | 1 | NA19089.hp2 | 5_prime_UTR_variant | MODIFIER | c.-368dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/11 | 105350 | INFO_REALIGN_3_PRIME | chrX | 7147846 | ||||
| chrX:7147854
|
G | GC | 1 | a0001c0001t0041 | 1 | NA19089.hp2 | 5_prime_UTR_variant | MODIFIER | c.-360dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/11 | 105342 | INFO_REALIGN_3_PRIME | chrX | 7147854 | ||||
| chrX:7147982
|
A | AC | 1 | a0001c0001t0014 | 1 | HG02738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-231dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/11 | 105213 | INFO_REALIGN_3_PRIME | chrX | 7147982 | ||||
| chrX:7148001
|
C | A | 1 | a0001c0001t0041 | 1 | NA19089.hp2 | 5_prime_UTR_variant | MODIFIER | c.-216C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/11 | 105199 | chrX | 7148001 | |||||
| chrX:7148010
|
A | C | 34 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(31): Show | 168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
5_prime_UTR_variant | MODIFIER | c.-207A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/11 | 105190 | chrX | 7148010 | |||||
| chrX:7148039
|
TG | T | 1 | a0002c0002t0020 | 1 | HG02257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-177delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/11 | 105160 | chrX | 7148039 | |||||
| chrX:7190989
|
C | T | 1 | a0001c0001t0019 | 1 | HG04228.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-24C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/11 | chrX | 7190989 | ||||||
| chrX:7350336
|
T | TG | 1 | a0001c0001t0039 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*79dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 80 | INFO_REALIGN_3_PRIME | chrX | 7350336 | ||||
| chrX:7350439
|
A | AG | 1 | a0001c0001t0039 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*183dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 184 | INFO_REALIGN_3_PRIME | chrX | 7350439 | ||||
| chrX:7350900
|
T | TAC | 1 | a0001c0001t0021 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*651_*652dupCA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 653 | INFO_REALIGN_3_PRIME | chrX | 7350900 | ||||
| chrX:7351103
|
A | G | 2 | a0001c0001t0038a0001c0001t0040 | 2 | HG03209.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*842A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 842 | chrX | 7351103 | |||||
| chrX:7351136
|
G | A | 1 | a0001c0001t0022 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*875G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 875 | chrX | 7351136 | |||||
| chrX:7351229
|
C | A | 1 | a0001c0001t0010 | 2 | HG02055.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*968C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 968 | chrX | 7351229 | |||||
| chrX:7351279
|
A | G | 5 | a0001c0001t0005a0001c0001t0037a0001c0001t0038others(2): Show | 12 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1018A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 1018 | chrX | 7351279 | |||||
| chrX:7351408
|
T | A | 1 | a0001c0001t0022 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1147T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 1147 | chrX | 7351408 | |||||
| chrX:7351846
|
G | A | 1 | a0001c0001t0008 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1585G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 1585 | chrX | 7351846 | |||||
| chrX:7351935
|
T | TA | 6 | a0001c0001t0004a0001c0001t0011a0001c0001t0015others(3): Show | 20 | HG00558.hp1 HG02056.hp1 HG03098.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1692dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 1693 | INFO_REALIGN_3_PRIME | chrX | 7351935 | ||||
| chrX:7351935
|
TA | T | 3 | a0001c0001t0009a0001c0001t0013a0001c0001t0035 | 5 | HG01169.hp2 HG01256.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1692delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 1692 | INFO_REALIGN_3_PRIME | chrX | 7351935 | ||||
| chrX:7351949
|
A | G | 1 | a0001c0001t0036 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1688A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 1688 | chrX | 7351949 | |||||
| chrX:7351950
|
AAAAG | A | 2 | a0001c0001t0033a0001c0001t0034 | 2 | HG02698.hp1 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1695_*1698delAAGA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 1695 | INFO_REALIGN_3_PRIME | chrX | 7351950 | ||||
| chrX:7352007
|
T | C | 1 | a0001c0001t0016 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1746T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 1746 | chrX | 7352007 | |||||
| chrX:7352092
|
A | G | 1 | a0001c0001t0018 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1831A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 1831 | chrX | 7352092 | |||||
| chrX:7352653
|
G | A | 3 | a0001c0001t0006a0001c0001t0012a0001c0001t0016 | 8 | HG00140.hp1 HG00639.hp2 HG01069.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2392G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 2392 | chrX | 7352653 | |||||
| chrX:7352920
|
G | T | 1 | a0001c0001t0035 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2659G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 2659 | chrX | 7352920 | |||||
| chrX:7352955
|
A | G | 26 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(23): Show | 137 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*2694A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 2694 | chrX | 7352955 | |||||
| chrX:7352956
|
C | CA | 1 | a0001c0001t0023 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2702dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 2703 | INFO_REALIGN_3_PRIME | chrX | 7352956 | ||||
| chrX:7352971
|
T | G | 1 | a0001c0001t0037 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2710T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 2710 | chrX | 7352971 | |||||
| chrX:7353093
|
A | T | 1 | a0001c0001t0028 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2832A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 2832 | chrX | 7353093 | |||||
| chrX:7353254
|
G | A | 1 | a0001c0001t0029 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2993G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 2993 | chrX | 7353254 | |||||
| chrX:7353267
|
C | T | 2 | a0001c0001t0023a0002c0002t0027 | 2 | HG01074.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3006C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 3006 | chrX | 7353267 | |||||
| chrX:7353275
|
G | A | 1 | a0001c0001t0030 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3014G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 3014 | chrX | 7353275 | |||||
| chrX:7353512
|
G | A | 1 | a0001c0001t0031 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3251G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 3251 | chrX | 7353512 | |||||
| chrX:7353663
|
C | T | 1 | a0001c0001t0026 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3402C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 3402 | chrX | 7353663 | |||||
| chrX:7353664
|
G | A | 1 | a0001c0001t0018 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3403G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 3403 | chrX | 7353664 | |||||
| chrX:7353808
|
C | T | 1 | a0001c0001t0033 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3547C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 3547 | chrX | 7353808 | |||||
| chrX:7354016
|
T | C | 1 | a0001c0001t0024 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3755T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 3755 | chrX | 7354016 | |||||
| chrX:7354102
|
C | G | 1 | a0001c0001t0032 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3841C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 3841 | chrX | 7354102 | |||||
| chrX:7354106
|
C | A | 1 | a0001c0001t0017 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3845C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 3845 | chrX | 7354106 | |||||
| chrX:7354184
|
G | A | 28 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(25): Show | 139 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*3923G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 3923 | chrX | 7354184 | |||||
| chrX:7354505
|
CT | C | 1 | a0001c0001t0025 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4247delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 11/11 | 4247 | INFO_REALIGN_3_PRIME | chrX | 7354505 |
| 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:7148162
|
A | AC | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-134+82dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7148162 | |||||
| chrX:7148169
|
C | G | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-134+86C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7148169 | ||||||
| chrX:7148170
|
G | C | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-134+87G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7148170 | ||||||
| chrX:7148355
|
G | GC | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-134+273dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7148355 | |||||
| chrX:7148478
|
A | G | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-134+395A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7148478 | ||||||
| chrX:7148563
|
C | G | 39 | a0001c0001t0001g0215a0001c0001t0002g0179a0001c0001t0002g0180others(36): Show | 39 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.-134+480C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7148563 | ||||||
| chrX:7148575
|
A | AG | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-134+494dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7148575 | |||||
| chrX:7148614
|
T | TG | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-134+534dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7148614 | |||||
| chrX:7148635
|
TC | T | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-134+555delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7148635 | |||||
| chrX:7148682
|
T | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-134+599T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7148682 | ||||||
| chrX:7148684
|
G | T | 1 | a0001c0001t0035g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-134+601G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7148684 | ||||||
| chrX:7148695
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-134+612C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7148695 | ||||||
| chrX:7148768
|
A | AG | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-134+686dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7148768 | |||||
| chrX:7148946
|
CT | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-134+875delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7148946 | |||||
| chrX:7148958
|
TC | T | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-134+878delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7148958 | |||||
| chrX:7149114
|
G | A | 1 | a0001c0001t0003g0101 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-134+1031G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7149114 | ||||||
| chrX:7149870
|
G | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(197): Show | 202 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.-134+1787G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7149870 | ||||||
| chrX:7150154
|
A | AT | 1 | a0001c0001t0014g0216 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-134+2078dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7150154 | |||||
| chrX:7150368
|
C | A | 1 | a0007c0004t0003g0150 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-134+2285C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7150368 | ||||||
| chrX:7150411
|
T | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-134+2328T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7150411 | ||||||
| chrX:7150488
|
T | C | 1 | a0001c0001t0002g0004 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-134+2405T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7150488 | ||||||
| chrX:7150740
|
T | TA | 4 | a0001c0001t0002g0179a0001c0001t0015g0102a0001c0001t0019g0103others(1): Show | 4 | HG02056.hp1 HG02976.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-134+2670dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7150740 | |||||
| chrX:7150740
|
TA | T | 2 | a0001c0001t0001g0149a0001c0001t0003g0148 | 2 | HG01243.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.-134+2670delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7150740 | |||||
| chrX:7150818
|
G | C | 1 | a0001c0001t0002g0180 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-134+2735G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7150818 | ||||||
| chrX:7150956
|
C | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-134+2873C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7150956 | ||||||
| chrX:7150997
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-134+2914G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7150997 | ||||||
| chrX:7151096
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-134+3013A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7151096 | ||||||
| chrX:7151311
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-134+3228G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7151311 | ||||||
| chrX:7151387
|
C | T | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-134+3304C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7151387 | ||||||
| chrX:7151488
|
C | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-134+3405C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7151488 | ||||||
| chrX:7151822
|
G | A | 1 | a0001c0001t0036g0006 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-134+3739G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7151822 | ||||||
| chrX:7151992
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-134+3909G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7151992 | ||||||
| chrX:7152151
|
AC | A | 1 | a0001c0001t0002g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-134+4070delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7152151 | |||||
| chrX:7152177
|
T | C | 1 | a0001c0001t0002g0106 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-134+4094T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7152177 | ||||||
| chrX:7152199
|
C | A | 1 | a0001c0001t0001g0001 | 2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.-134+4116C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7152199 | ||||||
| chrX:7152199
|
C | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(149): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-134+4116C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7152199 | ||||||
| chrX:7152203
|
C | T | 2 | a0003c0003t0003g0146a0003c0003t0003g0147 | 2 | NA18957.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-134+4120C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7152203 | ||||||
| chrX:7152204
|
A | G | 2 | a0003c0003t0003g0146a0003c0003t0003g0147 | 2 | NA18957.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-134+4121A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7152204 | ||||||
| chrX:7152241
|
C | A | 2 | a0001c0001t0003g0107a0001c0001t0003g0108 | 2 | HG02083.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-134+4158C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7152241 | ||||||
| chrX:7152242
|
A | G | 3 | a0001c0001t0002g0098a0001c0001t0003g0107a0001c0001t0003g0108 | 3 | HG02083.hp1 HG03139.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-134+4159A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7152242 | ||||||
| chrX:7152501
|
T | C | 1 | a0001c0001t0003g0151 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-134+4418T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7152501 | ||||||
| chrX:7152584
|
G | T | 3 | a0001c0001t0002g0144a0001c0001t0010g0100a0001c0001t0010g0145 | 3 | HG02055.hp1 HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-134+4501G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7152584 | ||||||
| chrX:7152696
|
G | C | 1 | a0001c0001t0003g0109 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-134+4613G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7152696 | ||||||
| chrX:7152809
|
CA | C | 1 | a0001c0001t0026g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-134+4732delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7152809 | |||||
| chrX:7153071
|
C | T | 1 | a0001c0001t0023g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-134+4988C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7153071 | ||||||
| chrX:7153471
|
CCTT | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-134+5391_-134+539 others(7): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7153471 | |||||
| chrX:7153538
|
CCTT | C | 1 | a0001c0001t0005g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-134+5458_-134+546 others(7): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7153538 | |||||
| chrX:7153569
|
C | T | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-134+5486C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7153569 | ||||||
| chrX:7153605
|
T | C | 1 | a0001c0001t0038g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-134+5522T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7153605 | ||||||
| chrX:7153745
|
TCTCCTTC others(5): Show |
T | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-134+5665_-134+567 others(16): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7153745 | |||||
| chrX:7153814
|
C | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(68): Show | 73 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.-134+5731C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7153814 | ||||||
| chrX:7153821
|
C | G | 1 | a0001c0001t0001g0073 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-134+5738C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7153821 | ||||||
| chrX:7153823
|
C | T | 14 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(11): Show | 14 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.-134+5740C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7153823 | ||||||
| chrX:7153959
|
C | T | 5 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG01109.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-134+5876C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7153959 | ||||||
| chrX:7153964
|
A | C | 66 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0215others(63): Show | 66 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.-134+5881A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7153964 | ||||||
| chrX:7154790
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(68): Show | 73 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.-134+6707G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7154790 | ||||||
| chrX:7154945
|
A | T | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-134+6862A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7154945 | ||||||
| chrX:7155021
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-134+6938A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7155021 | ||||||
| chrX:7155519
|
G | A | 1 | a0001c0001t0036g0006 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-134+7436G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7155519 | ||||||
| chrX:7155698
|
G | A | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-134+7615G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7155698 | ||||||
| chrX:7155740
|
CTG | C | 1 | a0001c0001t0001g0110 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-134+7660_-134+766 others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7155740 | |||||
| chrX:7155992
|
A | C | 1 | a0001c0001t0001g0054 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-134+7909A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7155992 | ||||||
| chrX:7156025
|
C | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(67): Show | 72 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.-134+7942C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7156025 | ||||||
| chrX:7156045
|
G | C | 1 | a0001c0001t0003g0152 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-134+7962G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7156045 | ||||||
| chrX:7156151
|
C | CA | 1 | a0001c0001t0002g0182 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-134+8082dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7156151 | |||||
| chrX:7156151
|
CA | C | 5 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0006g0176others(2): Show | 5 | HG01256.hp1 HG02735.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.-134+8082delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7156151 | |||||
| chrX:7156321
|
T | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-134+8238T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7156321 | ||||||
| chrX:7156822
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-134+8739A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7156822 | ||||||
| chrX:7156833
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-134+8750A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7156833 | ||||||
| chrX:7157365
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-134+9282T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7157365 | ||||||
| chrX:7157438
|
A | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-134+9355A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7157438 | ||||||
| chrX:7157752
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-134+9669A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7157752 | ||||||
| chrX:7157935
|
A | T | 1 | a0001c0001t0019g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-134+9852A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7157935 | ||||||
| chrX:7158107
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-134+10024G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7158107 | ||||||
| chrX:7158428
|
G | A | 1 | a0007c0004t0003g0150 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-134+10345G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7158428 | ||||||
| chrX:7158596
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-134+10513A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7158596 | ||||||
| chrX:7158635
|
T | C | 1 | a0001c0001t0002g0181 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-134+10552T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7158635 | ||||||
| chrX:7159053
|
G | T | 1 | a0001c0001t0003g0142 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-134+10970G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7159053 | ||||||
| chrX:7159114
|
C | CT | 1 | a0001c0001t0002g0095 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-134+11041dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7159114 | |||||
| chrX:7159182
|
AT | A | 2 | a0001c0001t0007g0153a0001c0001t0007g0154 | 2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.-134+11100delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7159182 | ||||||
| chrX:7159219
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-134+11136G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7159219 | ||||||
| chrX:7159305
|
T | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(135): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.-134+11222T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7159305 | ||||||
| chrX:7159305
|
T | G | 1 | a0001c0001t0002g0213 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-134+11222T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7159305 | ||||||
| chrX:7159374
|
A | T | 1 | a0001c0001t0001g0059 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-134+11291A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7159374 | ||||||
| chrX:7159924
|
G | C | 1 | a0001c0001t0006g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-134+11841G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7159924 | ||||||
| chrX:7160501
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-134+12418A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7160501 | ||||||
| chrX:7160627
|
C | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-134+12544C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7160627 | ||||||
| chrX:7160641
|
G | C | 1 | a0001c0001t0001g0010 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-134+12558G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7160641 | ||||||
| chrX:7160679
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-134+12596A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7160679 | ||||||
| chrX:7161036
|
A | G | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-134+12953A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7161036 | ||||||
| chrX:7161122
|
A | AT | 4 | a0001c0001t0003g0152a0001c0001t0003g0174a0001c0001t0003g0175others(1): Show | 4 | HG03831.hp2 NA18612.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.-134+13055dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7161122 | |||||
| chrX:7161122
|
AT | A | 11 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(8): Show | 11 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-134+13055delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7161122 | |||||
| chrX:7161122
|
ATT | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-134+13054_-134+13 others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7161122 | |||||
| chrX:7161295
|
T | C | 1 | a0001c0001t0002g0214 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-134+13212T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7161295 | ||||||
| chrX:7161326
|
C | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-134+13243C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7161326 | ||||||
| chrX:7161415
|
G | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-134+13332G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7161415 | ||||||
| chrX:7161606
|
A | T | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-134+13523A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7161606 | ||||||
| chrX:7161701
|
G | A | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-134+13618G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7161701 | ||||||
| chrX:7161894
|
G | T | 1 | a0001c0001t0002g0094 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-134+13811G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7161894 | ||||||
| chrX:7162265
|
A | G | 1 | a0001c0001t0002g0212 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-134+14182A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7162265 | ||||||
| chrX:7162577
|
G | A | 3 | a0001c0001t0003g0111a0001c0001t0003g0112a0001c0001t0003g0148 | 3 | HG02027.hp1 NA18951.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.-134+14494G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7162577 | ||||||
| chrX:7162607
|
G | A | 1 | a0001c0001t0003g0156 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-134+14524G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7162607 | ||||||
| chrX:7162768
|
C | T | 1 | a0001c0001t0024g0211 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-134+14685C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7162768 | ||||||
| chrX:7162773
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-134+14690G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7162773 | ||||||
| chrX:7162859
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-134+14776G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7162859 | ||||||
| chrX:7162874
|
G | A | 9 | a0001c0001t0003g0156a0001c0001t0003g0157a0001c0001t0003g0162others(6): Show | 9 | HG00140.hp1 HG00639.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.-134+14791G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7162874 | ||||||
| chrX:7162882
|
T | TA | 75 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(72): Show | 75 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.-134+14824dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7162882 | |||||
| chrX:7162882
|
T | TAA | 13 | a0001c0001t0001g0215a0001c0001t0002g0080a0001c0001t0002g0181others(10): Show | 13 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-134+14823_-134+14 others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7162882 | |||||
| chrX:7162882
|
T | TAAA | 1 | a0001c0001t0002g0183 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-134+14822_-134+14 others(9): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7162882 | |||||
| chrX:7162882
|
T | TAAAAA | 1 | a0001c0001t0004g0075 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-134+14820_-134+14 others(11): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7162882 | |||||
| chrX:7162882
|
T | TAAAAAA | 1 | a0001c0001t0004g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-134+14819_-134+14 others(12): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7162882 | |||||
| chrX:7162882
|
TA | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0048a0001c0001t0001g0052others(3): Show | 6 | HG00323.hp2 HG01515.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-134+14824delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7162882 | |||||
| chrX:7163056
|
C | CA | 3 | a0001c0001t0003g0115a0001c0001t0006g0158a0001c0001t0016g0159 | 3 | HG00639.hp2 HG01167.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-134+14994dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7163056 | |||||
| chrX:7163056
|
CA | C | 27 | a0001c0001t0001g0114a0001c0001t0002g0104a0001c0001t0002g0105others(24): Show | 27 | HG00738.hp1 HG01074.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.-134+14994delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7163056 | |||||
| chrX:7163056
|
CAA | C | 3 | a0001c0001t0001g0149a0001c0001t0005g0218a0001c0001t0005g0226 | 3 | HG01243.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-134+14993_-134+14 others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7163056 | |||||
| chrX:7163056
|
CAAAAA | C | 1 | a0001c0001t0002g0095 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-134+14990_-134+14 others(11): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7163056 | |||||
| chrX:7163056
|
CAAAAAA | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-134+14989_-134+14 others(12): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7163056 | |||||
| chrX:7163056
|
CAAAAAAA | C | 1 | a0001c0001t0004g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-134+14988_-134+14 others(13): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7163056 | |||||
| chrX:7163453
|
C | G | 5 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG01109.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-134+15370C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7163453 | ||||||
| chrX:7163558
|
A | G | 3 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0210 | 3 | HG03491.hp1 HG03492.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-134+15475A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7163558 | ||||||
| chrX:7163599
|
TCTC | T | 1 | a0001c0001t0001g0019 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-134+15517_-134+15 others(9): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7163599 | ||||||
| chrX:7163623
|
T | G | 1 | a0001c0001t0035g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-134+15540T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7163623 | ||||||
| chrX:7164451
|
T | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.-134+16368T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7164451 | ||||||
| chrX:7164483
|
A | C | 1 | a0001c0001t0002g0213 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-134+16400A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7164483 | ||||||
| chrX:7164506
|
T | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.-134+16423T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7164506 | ||||||
| chrX:7164562
|
C | A | 1 | a0001c0001t0023g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-134+16479C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7164562 | ||||||
| chrX:7164594
|
G | C | 1 | a0001c0001t0002g0181 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-134+16511G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7164594 | ||||||
| chrX:7164704
|
A | T | 1 | a0001c0001t0006g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-134+16621A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7164704 | ||||||
| chrX:7164746
|
G | T | 1 | a0001c0001t0023g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-134+16663G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7164746 | ||||||
| chrX:7164844
|
C | CA | 1 | a0001c0001t0006g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-134+16773dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7164844 | |||||
| chrX:7164844
|
CA | C | 1 | a0001c0001t0002g0217 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-134+16773delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7164844 | |||||
| chrX:7164844
|
CAA | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-134+16772_-134+16 others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7164844 | |||||
| chrX:7164855
|
A | C | 1 | a0004c0009t0002g0225 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-134+16772A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7164855 | ||||||
| chrX:7164887
|
G | A | 3 | a0001c0001t0002g0184a0001c0001t0002g0187a0001c0001t0002g0214 | 3 | HG00099.hp2 HG01123.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-134+16804G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7164887 | ||||||
| chrX:7165457
|
T | C | 67 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0215others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.-134+17374T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7165457 | ||||||
| chrX:7165865
|
C | A | 1 | a0001c0001t0003g0174 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-134+17782C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7165865 | ||||||
| chrX:7165870
|
G | A | 3 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0001t0002g0190 | 3 | HG01934.hp1 NA18981.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-134+17787G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7165870 | ||||||
| chrX:7166002
|
C | CT | 3 | a0001c0001t0001g0114a0001c0001t0002g0106a0001c0001t0003g0133 | 3 | HG01175.hp2 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-134+17938dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7166002 | |||||
| chrX:7166002
|
CT | C | 13 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0063others(10): Show | 13 | HG01256.hp1 HG02055.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-134+17938delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7166002 | |||||
| chrX:7166002
|
CTT | C | 1 | a0001c0001t0001g0062 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-134+17937_-134+17 others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7166002 | |||||
| chrX:7166014
|
T | A | 1 | a0001c0001t0002g0181 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-134+17931T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7166014 | ||||||
| chrX:7166264
|
T | G | 1 | a0001c0001t0004g0076 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-134+18181T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7166264 | ||||||
| chrX:7166393
|
A | G | 66 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0215others(63): Show | 66 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.-134+18310A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7166393 | ||||||
| chrX:7166474
|
G | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-134+18391G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7166474 | ||||||
| chrX:7167096
|
C | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | NA18957.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.-134+19013C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7167096 | ||||||
| chrX:7167255
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-134+19172G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7167255 | ||||||
| chrX:7167412
|
C | T | 1 | a0001c0001t0034g0045 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-134+19329C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7167412 | ||||||
| chrX:7167854
|
AT | A | 3 | a0001c0001t0001g0012a0001c0001t0021g0096a0001c0001t0041g0003 | 3 | HG00642.hp1 NA19058.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.-134+19783delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7167854 | |||||
| chrX:7168216
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(68): Show | 73 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.-134+20133G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7168216 | ||||||
| chrX:7168253
|
T | C | 1 | a0001c0001t0002g0212 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-134+20170T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7168253 | ||||||
| chrX:7168427
|
T | G | 1 | a0001c0001t0003g0112 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-134+20344T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7168427 | ||||||
| chrX:7168514
|
G | A | 13 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(10): Show | 13 | HG02055.hp1 HG02559.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.-134+20431G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7168514 | ||||||
| chrX:7168720
|
C | T | 2 | a0001c0001t0003g0131a0001c0001t0003g0132 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-134+20637C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7168720 | ||||||
| chrX:7169100
|
G | A | 1 | a0001c0001t0018g0141 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-134+21017G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7169100 | ||||||
| chrX:7169147
|
C | T | 1 | a0001c0001t0023g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-134+21064C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7169147 | ||||||
| chrX:7169153
|
C | T | 1 | a0001c0001t0002g0139 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-134+21070C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7169153 | ||||||
| chrX:7169260
|
TG | T | 1 | a0001c0001t0001g0008 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-134+21182delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7169260 | |||||
| chrX:7169594
|
C | A | 1 | a0001c0001t0033g0191 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-133-21286C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7169594 | ||||||
| chrX:7169893
|
T | TG | 3 | a0001c0001t0001g0044a0001c0001t0005g0218a0001c0001t0018g0141 | 3 | HG01433.hp1 HG02486.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-133-20979dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7169893 | |||||
| chrX:7169934
|
C | A | 2 | a0001c0001t0003g0115a0001c0001t0009g0120 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-133-20946C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7169934 | ||||||
| chrX:7169966
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-133-20914A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7169966 | ||||||
| chrX:7169979
|
G | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(69): Show | 74 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.-133-20901G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7169979 | ||||||
| chrX:7169990
|
A | C | 1 | a0001c0001t0038g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-133-20890A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7169990 | ||||||
| chrX:7170052
|
G | C | 2 | a0001c0001t0017g0121a0001c0001t0041g0003 | 2 | HG02132.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.-133-20828G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7170052 | ||||||
| chrX:7170333
|
C | CG | 2 | a0001c0001t0003g0157a0001c0001t0033g0191 | 2 | HG02698.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-133-20541dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7170333 | |||||
| chrX:7170375
|
A | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(67): Show | 72 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.-133-20505A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7170375 | ||||||
| chrX:7170595
|
G | A | 1 | a0001c0001t0004g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-133-20285G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7170595 | ||||||
| chrX:7170763
|
G | A | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-133-20117G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7170763 | ||||||
| chrX:7170818
|
C | T | 1 | a0005c0005t0003g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-133-20062C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7170818 | ||||||
| chrX:7171168
|
A | G | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064 | 3 | HG02922.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-133-19712A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7171168 | ||||||
| chrX:7171951
|
A | C | 1 | a0001c0001t0001g0053 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-133-18929A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7171951 | ||||||
| chrX:7172027
|
T | C | 1 | a0001c0001t0003g0107 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-133-18853T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7172027 | ||||||
| chrX:7172045
|
G | A | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-133-18835G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7172045 | ||||||
| chrX:7172302
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(159): Show | 164 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.-133-18578T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7172302 | ||||||
| chrX:7172444
|
C | T | 1 | a0001c0001t0015g0102 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-133-18436C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7172444 | ||||||
| chrX:7172502
|
G | C | 5 | a0001c0001t0001g0082a0001c0001t0002g0083a0001c0001t0004g0077others(2): Show | 5 | HG00558.hp1 NA19005.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.-133-18378G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7172502 | ||||||
| chrX:7172567
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-133-18313G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7172567 | ||||||
| chrX:7172669
|
A | G | 1 | a0001c0001t0037g0224 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-133-18211A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7172669 | ||||||
| chrX:7172762
|
G | T | 1 | a0001c0001t0002g0190 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-133-18118G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7172762 | ||||||
| chrX:7172774
|
C | T | 1 | a0002c0002t0020g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-133-18106C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7172774 | ||||||
| chrX:7172997
|
CAT | C | 8 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0222others(5): Show | 8 | HG01074.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-133-17882_-133-17 others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7172997 | ||||||
| chrX:7173051
|
T | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(145): Show | 150 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.-133-17829T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7173051 | ||||||
| chrX:7173094
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-133-17786A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7173094 | ||||||
| chrX:7173139
|
G | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(225): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.-133-17741G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7173139 | ||||||
| chrX:7173160
|
A | G | 1 | a0001c0001t0003g0152 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-133-17720A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7173160 | ||||||
| chrX:7173239
|
C | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-133-17641C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7173239 | ||||||
| chrX:7173249
|
T | A | 1 | a0001c0001t0002g0139 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-133-17631T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7173249 | ||||||
| chrX:7173405
|
G | A | 9 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0067others(6): Show | 9 | HG00099.hp1 HG00639.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-133-17475G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7173405 | ||||||
| chrX:7173547
|
A | T | 1 | a0001c0001t0031g0018 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-133-17333A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7173547 | ||||||
| chrX:7173614
|
CTT | C | 2 | a0001c0001t0005g0218a0001c0001t0005g0226 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-133-17262_-133-17 others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7173614 | |||||
| chrX:7174361
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-133-16519C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7174361 | ||||||
| chrX:7174679
|
A | G | 1 | a0001c0001t0003g0156 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-133-16201A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7174679 | ||||||
| chrX:7175179
|
T | TA | 9 | a0001c0001t0001g0013a0001c0001t0002g0104a0001c0001t0003g0111others(6): Show | 9 | HG00558.hp2 HG01074.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.-133-15676dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7175179 | |||||
| chrX:7175179
|
TA | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(128): Show | 133 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.-133-15676delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7175179 | |||||
| chrX:7175179
|
TAA | T | 4 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 4 | HG01192.hp1 HG01433.hp1 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.-133-15677_-133-15 others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7175179 | |||||
| chrX:7175470
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0149 | 2 | HG01243.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-133-15410G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7175470 | ||||||
| chrX:7175493
|
C | CAACAA | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(138): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.-133-15368_-133-15 others(11): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7175493 | |||||
| chrX:7175493
|
C | CAACAAAA others(3): Show |
4 | a0001c0001t0002g0183a0001c0001t0002g0185a0001c0001t0013g0051others(1): Show | 4 | HG01256.hp1 HG02257.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.-133-15373_-133-15 others(16): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7175493 | |||||
| chrX:7175500
|
A | ACAAAG | 4 | a0001c0001t0005g0221a0001c0001t0035g0229a0001c0001t0037g0224others(1): Show | 4 | HG01106.hp1 HG02145.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-133-15376_-133-15 others(11): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7175500 | |||||
| chrX:7175643
|
C | T | 1 | a0001c0001t0002g0213 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-133-15237C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7175643 | ||||||
| chrX:7175675
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-133-15205A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7175675 | ||||||
| chrX:7176450
|
G | A | 1 | a0002c0002t0020g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-133-14430G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7176450 | ||||||
| chrX:7176550
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(4): Show | 8 | HG02129.hp1 NA18940.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.-133-14330G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7176550 | ||||||
| chrX:7176643
|
C | CA | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(67): Show | 72 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.-133-14235dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7176643 | |||||
| chrX:7176681
|
G | C | 1 | a0001c0001t0005g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-133-14199G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7176681 | ||||||
| chrX:7176916
|
A | C | 1 | a0001c0001t0003g0108 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-133-13964A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7176916 | ||||||
| chrX:7177406
|
GTCA | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-133-13469_-133-13 others(9): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7177406 | |||||
| chrX:7177429
|
CAT | C | 1 | a0001c0001t0037g0224 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-133-13447_-133-13 others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7177429 | |||||
| chrX:7177447
|
A | AAT | 1 | a0001c0001t0003g0152 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-133-13422_-133-13 others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7177447 | |||||
| chrX:7177479
|
A | AT | 2 | a0001c0001t0001g0110a0001c0001t0001g0130 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-133-13392dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7177479 | |||||
| chrX:7177479
|
A | T | 3 | a0001c0001t0002g0144a0001c0001t0010g0100a0001c0001t0010g0145 | 3 | HG02055.hp1 HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-133-13401A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7177479 | ||||||
| chrX:7177481
|
T | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(83): Show | 88 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.-133-13399T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7177481 | ||||||
| chrX:7177483
|
T | A | 11 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(8): Show | 11 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-133-13397T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7177483 | ||||||
| chrX:7177503
|
G | A | 1 | a0001c0001t0002g0212 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-133-13377G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7177503 | ||||||
| chrX:7177789
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-133-13091A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7177789 | ||||||
| chrX:7177825
|
A | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG01192.hp1 HG01361.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.-133-13055A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7177825 | ||||||
| chrX:7177838
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-133-13042A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7177838 | ||||||
| chrX:7177984
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-133-12896G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7177984 | ||||||
| chrX:7178983
|
C | G | 1 | a0001c0001t0002g0207 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-133-11897C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7178983 | ||||||
| chrX:7179553
|
AC | A | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-133-11324delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7179553 | |||||
| chrX:7179725
|
A | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0024 | 2 | NA18988.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-133-11155A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7179725 | ||||||
| chrX:7180014
|
A | T | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-133-10866A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7180014 | ||||||
| chrX:7180074
|
CT | C | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-133-10803delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7180074 | |||||
| chrX:7180262
|
G | A | 3 | a0001c0001t0003g0166a0001c0001t0007g0153a0001c0001t0007g0154 | 3 | HG00280.hp1 HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-133-10618G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7180262 | ||||||
| chrX:7180270
|
C | T | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-133-10610C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7180270 | ||||||
| chrX:7180700
|
C | T | 1 | a0001c0001t0016g0159 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-133-10180C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7180700 | ||||||
| chrX:7181014
|
C | T | 1 | a0001c0001t0002g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-133-9866C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7181014 | ||||||
| chrX:7181022
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-133-9858A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7181022 | ||||||
| chrX:7181120
|
A | C | 1 | a0001c0001t0002g0095 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-133-9760A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7181120 | ||||||
| chrX:7181224
|
C | T | 1 | a0001c0001t0018g0141 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-133-9656C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7181224 | ||||||
| chrX:7181265
|
TA | T | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-133-9610delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7181265 | |||||
| chrX:7181288
|
G | GT | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-133-9586dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7181288 | |||||
| chrX:7181368
|
T | C | 66 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0215others(63): Show | 66 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.-133-9512T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7181368 | ||||||
| chrX:7181389
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-133-9491A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7181389 | ||||||
| chrX:7181513
|
GA | G | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-133-9365delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7181513 | |||||
| chrX:7181684
|
T | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(136): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.-133-9196T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7181684 | ||||||
| chrX:7181762
|
AG | A | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-133-9115delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7181762 | |||||
| chrX:7181884
|
G | A | 1 | a0001c0001t0002g0106 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-133-8996G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7181884 | ||||||
| chrX:7181937
|
G | A | 15 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(12): Show | 15 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.-133-8943G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7181937 | ||||||
| chrX:7182087
|
C | T | 1 | a0001c0001t0035g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-133-8793C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7182087 | ||||||
| chrX:7182099
|
A | AG | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-133-8781_-133-878 others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7182099 | ||||||
| chrX:7182386
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-133-8494T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7182386 | ||||||
| chrX:7182868
|
A | AT | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-133-8010dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7182868 | |||||
| chrX:7182891
|
C | CG | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-133-7989_-133-798 others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7182891 | ||||||
| chrX:7183031
|
C | G | 1 | a0001c0001t0002g0207 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-133-7849C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7183031 | ||||||
| chrX:7183245
|
TC | T | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-133-7631delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7183245 | |||||
| chrX:7183484
|
T | TC | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-133-7395dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7183484 | |||||
| chrX:7183487
|
C | T | 1 | a0001c0001t0023g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-133-7393C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7183487 | ||||||
| chrX:7183864
|
TG | T | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-133-7014delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7183864 | |||||
| chrX:7184012
|
TA | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(68): Show | 73 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.-133-6857delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7184012 | |||||
| chrX:7184012
|
TAA | T | 1 | a0001c0001t0036g0006 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-133-6858_-133-685 others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7184012 | |||||
| chrX:7184358
|
TC | T | 2 | a0001c0001t0002g0182a0001c0001t0002g0206 | 2 | HG00609.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.-133-6519delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7184358 | |||||
| chrX:7184443
|
TA | T | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-133-6432delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7184443 | |||||
| chrX:7184448
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-133-6432A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7184448 | ||||||
| chrX:7184581
|
CT | C | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-133-6297delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7184581 | |||||
| chrX:7184809
|
G | T | 1 | a0001c0001t0002g0213 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-133-6071G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7184809 | ||||||
| chrX:7185165
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-133-5715T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7185165 | ||||||
| chrX:7185198
|
TG | T | 1 | a0001c0001t0002g0194 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-133-5681delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7185198 | ||||||
| chrX:7185242
|
C | A | 1 | a0002c0002t0020g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-133-5638C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7185242 | ||||||
| chrX:7185321
|
A | C | 2 | a0001c0001t0002g0182a0001c0001t0002g0206 | 2 | HG00609.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.-133-5559A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7185321 | ||||||
| chrX:7185432
|
G | A | 1 | a0001c0001t0002g0212 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-133-5448G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7185432 | ||||||
| chrX:7185871
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-133-5009G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7185871 | ||||||
| chrX:7186471
|
G | A | 2 | a0001c0001t0002g0183a0001c0001t0002g0185 | 2 | NA19066.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-133-4409G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7186471 | ||||||
| chrX:7186710
|
G | C | 1 | a0001c0001t0001g0010 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-133-4170G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7186710 | ||||||
| chrX:7186771
|
G | A | 1 | a0001c0001t0005g0056 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-133-4109G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7186771 | ||||||
| chrX:7186848
|
T | C | 1 | a0001c0001t0028g0195 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-133-4032T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7186848 | ||||||
| chrX:7186918
|
G | A | 2 | a0001c0001t0003g0115a0001c0001t0009g0120 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-133-3962G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7186918 | ||||||
| chrX:7187322
|
A | G | 1 | a0001c0001t0015g0102 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-133-3558A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7187322 | ||||||
| chrX:7187678
|
A | G | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-133-3202A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7187678 | ||||||
| chrX:7187828
|
A | G | 1 | a0001c0001t0035g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-133-3052A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7187828 | ||||||
| chrX:7188165
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(68): Show | 73 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.-133-2715G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7188165 | ||||||
| chrX:7188460
|
T | C | 1 | a0001c0001t0002g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-133-2420T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7188460 | ||||||
| chrX:7188664
|
T | TG | 1 | a0001c0001t0001g0040 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-133-2210dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7188664 | |||||
| chrX:7189158
|
A | AT | 1 | a0001c0001t0003g0174 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-133-1713dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7189158 | |||||
| chrX:7189541
|
C | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(161): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-133-1339C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7189541 | ||||||
| chrX:7189568
|
A | G | 1 | a0001c0001t0040g0227 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-133-1312A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7189568 | ||||||
| chrX:7189837
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-133-1043A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7189837 | ||||||
| chrX:7189896
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-133-984G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7189896 | ||||||
| chrX:7190006
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-133-874T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7190006 | ||||||
| chrX:7190767
|
C | CA | 3 | a0001c0001t0002g0184a0001c0001t0002g0187a0001c0001t0002g0214 | 3 | HG00099.hp2 HG01123.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-133-102dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7190767 | |||||
| chrX:7190767
|
CA | C | 1 | a0001c0001t0004g0093 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-133-102delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 7190767 | |||||
| chrX:7190809
|
A | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-133-71A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 1/10 | chrX | 7190809 | ||||||
| chrX:7191042
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-5+34G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7191042 | ||||||
| chrX:7191154
|
T | C | 1 | a0001c0001t0001g0025 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-5+146T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7191154 | ||||||
| chrX:7191210
|
TC | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(67): Show | 72 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.-5+203delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7191210 | ||||||
| chrX:7191226
|
G | A | 1 | a0001c0001t0022g0065 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-5+218G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7191226 | ||||||
| chrX:7191227
|
TG | T | 1 | a0001c0001t0001g0066 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-5+223delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7191227 | |||||
| chrX:7191342
|
T | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-5+334T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7191342 | ||||||
| chrX:7191512
|
T | C | 1 | a0001c0001t0035g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-5+504T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7191512 | ||||||
| chrX:7191648
|
TC | T | 1 | a0001c0001t0002g0205 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-5+645delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7191648 | |||||
| chrX:7191736
|
GC | G | 5 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0222others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+729delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7191736 | ||||||
| chrX:7191778
|
A | C | 1 | a0001c0001t0001g0052 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-5+770A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7191778 | ||||||
| chrX:7191826
|
C | T | 9 | a0001c0001t0003g0101a0001c0001t0003g0109a0001c0001t0003g0113others(6): Show | 9 | HG00738.hp1 HG01081.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+818C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7191826 | ||||||
| chrX:7192069
|
A | G | 3 | a0001c0001t0002g0204a0001c0001t0002g0207a0001c0001t0004g0193 | 3 | NA18960.hp1 NA19070.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-5+1061A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7192069 | ||||||
| chrX:7192313
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(136): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.-5+1305C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7192313 | ||||||
| chrX:7192563
|
C | CA | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(138): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.-5+1570dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7192563 | |||||
| chrX:7192563
|
C | CAA | 5 | a0001c0001t0002g0095a0001c0001t0004g0081a0001c0001t0005g0221others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+1569_-5+1570dup others(2): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7192563 | |||||
| chrX:7192659
|
G | A | 2 | a0001c0001t0005g0218a0001c0001t0005g0226 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-5+1651G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7192659 | ||||||
| chrX:7192695
|
C | T | 1 | a0001c0001t0038g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-5+1687C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7192695 | ||||||
| chrX:7192740
|
G | A | 1 | a0001c0001t0035g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-5+1732G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7192740 | ||||||
| chrX:7193043
|
A | G | 67 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0215others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.-5+2035A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7193043 | ||||||
| chrX:7193233
|
G | C | 1 | a0001c0001t0002g0207 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-5+2225G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7193233 | ||||||
| chrX:7193367
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(4): Show | 8 | HG00621.hp1 HG01081.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5+2359G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7193367 | ||||||
| chrX:7193376
|
T | TTTG | 1 | a0001c0001t0001g0050 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-5+2389_-5+2391dup others(3): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7193376 | |||||
| chrX:7193451
|
C | CT | 67 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0215others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.-5+2455dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7193451 | |||||
| chrX:7193611
|
A | C | 1 | a0001c0001t0002g0208 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-5+2603A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7193611 | ||||||
| chrX:7193614
|
C | A | 1 | a0001c0001t0002g0208 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-5+2606C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7193614 | ||||||
| chrX:7193616
|
T | A | 1 | a0001c0001t0002g0208 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-5+2608T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7193616 | ||||||
| chrX:7193617
|
TC | T | 1 | a0001c0001t0002g0208 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-5+2611delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7193617 | |||||
| chrX:7193942
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-5+2934C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7193942 | ||||||
| chrX:7194006
|
G | A | 3 | a0001c0001t0003g0156a0001c0001t0003g0157a0001c0001t0003g0162 | 3 | HG01261.hp1 HG03017.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-5+2998G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7194006 | ||||||
| chrX:7194246
|
CGTT | C | 12 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(9): Show | 12 | HG02055.hp1 HG02647.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.-5+3241_-5+3243del others(3): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7194246 | |||||
| chrX:7194293
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0036g0006 | 2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-5+3285C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7194293 | ||||||
| chrX:7194359
|
T | A | 9 | a0001c0001t0003g0111a0001c0001t0003g0112a0001c0001t0003g0122others(6): Show | 9 | HG02027.hp1 HG02132.hp1 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5+3351T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7194359 | ||||||
| chrX:7194501
|
C | G | 1 | a0001c0001t0003g0107 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-5+3493C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7194501 | ||||||
| chrX:7194560
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-5+3552G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7194560 | ||||||
| chrX:7194645
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-5+3637C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7194645 | ||||||
| chrX:7194674
|
G | T | 30 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(27): Show | 31 | HG00558.hp2 HG01256.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.-5+3666G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7194674 | ||||||
| chrX:7194873
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-5+3865C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7194873 | ||||||
| chrX:7195267
|
A | G | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(69): Show | 74 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.-5+4259A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7195267 | ||||||
| chrX:7195382
|
T | G | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5+4374T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7195382 | ||||||
| chrX:7195693
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-5+4685C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7195693 | ||||||
| chrX:7195718
|
T | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0130 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-5+4710T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7195718 | ||||||
| chrX:7195722
|
G | A | 2 | a0001c0001t0003g0107a0001c0001t0003g0108 | 2 | HG02083.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-5+4714G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7195722 | ||||||
| chrX:7195750
|
C | T | 1 | a0001c0001t0035g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-5+4742C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7195750 | ||||||
| chrX:7195761
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-5+4753G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7195761 | ||||||
| chrX:7196105
|
T | TAGA | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-5+5099_-5+5100ins others(3): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7196105 | |||||
| chrX:7196174
|
A | G | 2 | a0003c0003t0003g0146a0003c0003t0003g0147 | 2 | NA18957.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-5+5166A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7196174 | ||||||
| chrX:7196283
|
C | CAACCTTA others(5): Show |
1 | a0001c0001t0003g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-5+5276_-5+5287dup others(12): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7196283 | |||||
| chrX:7196512
|
TA | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-5+5515delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7196512 | |||||
| chrX:7196540
|
T | C | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(68): Show | 73 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.-5+5532T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7196540 | ||||||
| chrX:7196653
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-5+5645G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7196653 | ||||||
| chrX:7196744
|
GTCTC | G | 1 | a0001c0001t0002g0095 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-5+5740_-5+5743del others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7196744 | |||||
| chrX:7196829
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-5+5821C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7196829 | ||||||
| chrX:7197052
|
A | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-5+6044A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7197052 | ||||||
| chrX:7197693
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-5+6685G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7197693 | ||||||
| chrX:7197856
|
C | CTACT | 1 | a0001c0001t0015g0102 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-5+6849_-5+6852dup others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7197856 | |||||
| chrX:7197871
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-5+6863G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7197871 | ||||||
| chrX:7198005
|
A | G | 1 | a0001c0001t0002g0139 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-5+6997A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7198005 | ||||||
| chrX:7198063
|
AC | A | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-5+7062delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7198063 | |||||
| chrX:7198072
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-5+7064A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7198072 | ||||||
| chrX:7198279
|
G | A | 1 | a0001c0001t0002g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-5+7271G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7198279 | ||||||
| chrX:7198477
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-5+7469G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7198477 | ||||||
| chrX:7198512
|
A | G | 1 | a0001c0001t0003g0163 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-5+7504A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7198512 | ||||||
| chrX:7198551
|
TC | T | 1 | a0001c0001t0003g0123 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-5+7547delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7198551 | |||||
| chrX:7198572
|
T | C | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5+7564T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7198572 | ||||||
| chrX:7198671
|
T | A | 1 | a0001c0001t0001g0001 | 2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.-5+7663T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7198671 | ||||||
| chrX:7198917
|
G | GT | 1 | a0001c0001t0003g0133 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-5+7922dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7198917 | |||||
| chrX:7198962
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-5+7954T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7198962 | ||||||
| chrX:7199247
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-5+8239T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7199247 | ||||||
| chrX:7199327
|
AT | A | 1 | a0001c0001t0003g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-5+8323delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7199327 | |||||
| chrX:7199550
|
TG | T | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-5+8545delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7199550 | |||||
| chrX:7199644
|
A | G | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-5+8636A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7199644 | ||||||
| chrX:7199876
|
TA | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(225): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.-5+8879delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7199876 | |||||
| chrX:7199900
|
TA | T | 5 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG01109.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+8896delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7199900 | |||||
| chrX:7200016
|
A | G | 2 | a0001c0001t0002g0203a0001c0001t0005g0223 | 2 | HG01070.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-5+9008A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7200016 | ||||||
| chrX:7200058
|
CT | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(137): Show | 142 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.-5+9064delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7200058 | |||||
| chrX:7200058
|
CTT | C | 13 | a0001c0001t0001g0067a0001c0001t0005g0218a0001c0001t0005g0220others(10): Show | 13 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5+9063_-5+9064del others(2): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7200058 | |||||
| chrX:7200521
|
G | T | 2 | a0001c0001t0004g0084a0001c0001t0004g0085 | 2 | NA19005.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-5+9513G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7200521 | ||||||
| chrX:7200701
|
T | TG | 1 | a0001c0001t0003g0123 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-5+9698dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7200701 | |||||
| chrX:7200789
|
C | T | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-5+9781C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7200789 | ||||||
| chrX:7200954
|
G | GTGGA | 81 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0215others(78): Show | 81 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-5+9977_-5+9980dup others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7200954 | |||||
| chrX:7200954
|
G | GTGGATGG others(5): Show |
1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-5+9969_-5+9980dup others(12): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7200954 | |||||
| chrX:7200954
|
GTGGA | G | 3 | a0001c0001t0001g0030a0001c0001t0003g0169a0001c0001t0009g0170 | 3 | HG02135.hp1 NA18965.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-5+9977_-5+9980del others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7200954 | |||||
| chrX:7201083
|
T | C | 1 | a0001c0001t0002g0186 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-5+10075T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7201083 | ||||||
| chrX:7201259
|
GGATA | G | 1 | a0001c0001t0005g0138 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-5+10261_-5+10264d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7201259 | |||||
| chrX:7201377
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-5+10369A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7201377 | ||||||
| chrX:7201460
|
A | AT | 9 | a0001c0001t0003g0101a0001c0001t0003g0109a0001c0001t0003g0113others(6): Show | 9 | HG00738.hp1 HG01081.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+10461dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7201460 | |||||
| chrX:7201624
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-5+10616A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7201624 | ||||||
| chrX:7201720
|
A | G | 1 | a0001c0001t0026g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-5+10712A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7201720 | ||||||
| chrX:7202374
|
C | T | 1 | a0001c0001t0002g0212 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-5+11366C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7202374 | ||||||
| chrX:7202380
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-5+11372A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7202380 | ||||||
| chrX:7202402
|
T | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0024 | 2 | NA18988.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-5+11394T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7202402 | ||||||
| chrX:7202815
|
A | T | 1 | a0001c0001t0003g0128 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-5+11807A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7202815 | ||||||
| chrX:7203347
|
T | TA | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(67): Show | 72 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.-5+12346dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7203347 | |||||
| chrX:7203517
|
G | A | 1 | a0002c0002t0020g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-5+12509G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7203517 | ||||||
| chrX:7203789
|
T | G | 1 | a0001c0001t0023g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-5+12781T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7203789 | ||||||
| chrX:7203791
|
T | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 64 | HG00558.hp1 HG01074.hp1 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.-5+12783T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7203791 | ||||||
| chrX:7203793
|
G | T | 23 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(20): Show | 23 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5+12785G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7203793 | ||||||
| chrX:7203959
|
C | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-5+12951C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7203959 | ||||||
| chrX:7204034
|
A | C | 1 | a0001c0001t0002g0139 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-5+13026A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204034 | ||||||
| chrX:7204074
|
C | G | 1 | a0001c0001t0003g0174 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-5+13066C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204074 | ||||||
| chrX:7204181
|
A | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.-5+13173A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204181 | ||||||
| chrX:7204303
|
TA | T | 1 | a0001c0001t0030g0038 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-5+13300delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7204303 | |||||
| chrX:7204473
|
TTTCCTTC others(9): Show |
T | 1 | a0001c0001t0040g0227 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-5+13483_-5+13498d others(18): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7204473 | |||||
| chrX:7204481
|
CTCCCTCC others(21): Show |
C | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-5+13475_-5+13502d others(30): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7204481 | |||||
| chrX:7204483
|
C | T | 78 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0215others(75): Show | 78 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-5+13475C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204483 | ||||||
| chrX:7204489
|
C | G | 1 | a0001c0001t0001g0050 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-5+13481C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204489 | ||||||
| chrX:7204495
|
TCCTCCCT others(21): Show |
T | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0011g0026 | 3 | HG00621.hp1 NA18975.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-5+13501_-5+13528d others(30): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7204495 | |||||
| chrX:7204498
|
TC | T | 1 | a0001c0001t0030g0038 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-5+13493delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7204498 | |||||
| chrX:7204525
|
C | G | 11 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(8): Show | 11 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5+13517C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204525 | ||||||
| chrX:7204549
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-5+13541C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204549 | ||||||
| chrX:7204684
|
C | A | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-5+13676C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204684 | ||||||
| chrX:7204685
|
C | G | 14 | a0001c0001t0001g0082a0001c0001t0002g0083a0001c0001t0004g0074others(11): Show | 14 | HG00558.hp1 NA18943.hp1 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.-5+13677C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204685 | ||||||
| chrX:7204714
|
C | T | 1 | a0002c0002t0020g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-5+13706C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204714 | ||||||
| chrX:7204715
|
A | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.-5+13707A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204715 | ||||||
| chrX:7204731
|
T | C | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5+13723T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204731 | ||||||
| chrX:7204767
|
C | G | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5+13759C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204767 | ||||||
| chrX:7204783
|
C | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0068others(2): Show | 5 | HG02630.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+13775C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204783 | ||||||
| chrX:7204786
|
C | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0130 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-5+13778C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204786 | ||||||
| chrX:7204840
|
C | G | 1 | a0006c0007t0001g0039 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-5+13832C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204840 | ||||||
| chrX:7204923
|
AAT | A | 1 | a0001c0001t0001g0037 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-5+13916_-5+13917d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204923 | ||||||
| chrX:7204926
|
C | G | 1 | a0004c0009t0002g0225 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-5+13918C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204926 | ||||||
| chrX:7204927
|
AG | A | 1 | a0001c0001t0001g0037 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-5+13920delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204927 | ||||||
| chrX:7204931
|
A | G | 51 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0040others(48): Show | 51 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-5+13923A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204931 | ||||||
| chrX:7204932
|
CTTATGAT others(335): Show |
C | 1 | a0001c0001t0001g0037 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-5+13925_-5+14266d others(2): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7204932 | ||||||
| chrX:7205023
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0011g0026 | 3 | HG00621.hp1 NA18975.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-5+14015C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7205023 | ||||||
| chrX:7205044
|
C | G | 42 | a0001c0001t0001g0110a0001c0001t0001g0114a0001c0001t0001g0130others(39): Show | 42 | HG00140.hp1 HG00639.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.-5+14036C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7205044 | ||||||
| chrX:7205121
|
G | C | 2 | a0001c0001t0035g0229a0001c0001t0037g0224 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-5+14113G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7205121 | ||||||
| chrX:7205156
|
A | G | 1 | a0001c0001t0019g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-5+14148A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7205156 | ||||||
| chrX:7205264
|
G | C | 70 | a0001c0001t0001g0031a0001c0001t0001g0058a0001c0001t0001g0082others(67): Show | 70 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-5+14256G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7205264 | ||||||
| chrX:7205277
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0037 | 2 | HG02723.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-5+14269T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7205277 | ||||||
| chrX:7205278
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0037 | 2 | HG02723.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-5+14270G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7205278 | ||||||
| chrX:7205291
|
T | C | 2 | a0001c0001t0003g0124a0001c0001t0004g0089 | 2 | NA18943.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-5+14283T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7205291 | ||||||
| chrX:7205310
|
C | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(140): Show | 145 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.-5+14302C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7205310 | ||||||
| chrX:7205380
|
G | A | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-5+14372G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7205380 | ||||||
| chrX:7205438
|
T | C | 2 | a0001c0001t0003g0116a0001c0001t0003g0117 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-5+14430T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7205438 | ||||||
| chrX:7205487
|
G | C | 10 | a0001c0001t0003g0101a0001c0001t0003g0109a0001c0001t0003g0113others(7): Show | 10 | HG00738.hp1 HG01081.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.-5+14479G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7205487 | ||||||
| chrX:7205551
|
G | A | 1 | a0001c0001t0005g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-5+14543G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7205551 | ||||||
| chrX:7205581
|
GTTTTCT | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(106): Show | 111 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.-5+14595_-5+14600d others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7205581 | |||||
| chrX:7205641
|
C | CT | 14 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(11): Show | 15 | HG01074.hp1 HG01106.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.-5+14648dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7205641 | |||||
| chrX:7205641
|
C | CTT | 4 | a0001c0001t0005g0221a0001c0001t0005g0222a0001c0001t0005g0223others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+14647_-5+14648d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7205641 | |||||
| chrX:7205641
|
C | CTTT | 3 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0226 | 3 | HG02109.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-5+14646_-5+14648d others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7205641 | |||||
| chrX:7205641
|
CT | C | 5 | a0001c0001t0002g0099a0001c0001t0002g0203a0001c0001t0013g0051others(2): Show | 5 | HG01070.hp2 HG01256.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+14648delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7205641 | |||||
| chrX:7205641
|
CTT | C | 64 | a0001c0001t0001g0082a0001c0001t0001g0215a0001c0001t0002g0004others(61): Show | 64 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.-5+14647_-5+14648d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7205641 | |||||
| chrX:7205641
|
CTTT | C | 1 | a0001c0001t0004g0078 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-5+14646_-5+14648d others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7205641 | |||||
| chrX:7205772
|
T | C | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-5+14764T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7205772 | ||||||
| chrX:7205845
|
G | C | 1 | a0001c0001t0004g0093 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-5+14837G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7205845 | ||||||
| chrX:7205855
|
A | G | 1 | a0001c0001t0015g0102 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-5+14847A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7205855 | ||||||
| chrX:7205932
|
T | C | 1 | a0001c0001t0005g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-5+14924T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7205932 | ||||||
| chrX:7205943
|
G | T | 1 | a0001c0001t0004g0089 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-5+14935G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7205943 | ||||||
| chrX:7206001
|
T | C | 1 | a0001c0001t0005g0056 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-5+14993T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7206001 | ||||||
| chrX:7206244
|
G | C | 5 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0068others(2): Show | 5 | HG02630.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+15236G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7206244 | ||||||
| chrX:7206300
|
T | C | 1 | a0001c0001t0035g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-5+15292T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7206300 | ||||||
| chrX:7206347
|
A | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(67): Show | 72 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.-5+15339A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7206347 | ||||||
| chrX:7206353
|
G | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-5+15345G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7206353 | ||||||
| chrX:7206356
|
G | C | 1 | a0001c0001t0035g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-5+15348G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7206356 | ||||||
| chrX:7206394
|
G | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-5+15386G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7206394 | ||||||
| chrX:7206658
|
G | C | 2 | a0001c0001t0003g0115a0001c0001t0009g0120 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-5+15650G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7206658 | ||||||
| chrX:7207029
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(137): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.-5+16021G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7207029 | ||||||
| chrX:7207076
|
A | G | 1 | a0001c0001t0033g0191 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-5+16068A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7207076 | ||||||
| chrX:7207152
|
T | C | 1 | a0001c0001t0005g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-5+16144T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7207152 | ||||||
| chrX:7207190
|
T | TA | 1 | a0001c0001t0022g0065 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-5+16193dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7207190 | |||||
| chrX:7208346
|
T | C | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-5+17338T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7208346 | ||||||
| chrX:7208489
|
G | A | 68 | a0001c0001t0001g0082a0001c0001t0001g0215a0001c0001t0002g0004others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-5+17481G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7208489 | ||||||
| chrX:7208549
|
G | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0070 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-5+17541G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7208549 | ||||||
| chrX:7208818
|
G | C | 2 | a0001c0001t0001g0114a0001c0001t0001g0149 | 2 | HG01243.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-5+17810G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7208818 | ||||||
| chrX:7209271
|
A | G | 8 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0222others(5): Show | 8 | HG01074.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5+18263A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7209271 | ||||||
| chrX:7209454
|
TTAAA | T | 1 | a0001c0001t0010g0145 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-5+18453_-5+18456d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7209454 | |||||
| chrX:7209501
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(225): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.-5+18493G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7209501 | ||||||
| chrX:7209552
|
T | TAC | 157 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(154): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-5+18545_-5+18546i others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7209552 | |||||
| chrX:7209738
|
G | T | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5+18730G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7209738 | ||||||
| chrX:7209754
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-5+18746C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7209754 | ||||||
| chrX:7209777
|
A | AC | 2 | a0001c0001t0001g0014a0001c0001t0004g0078 | 2 | NA18966.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-5+18774dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7209777 | |||||
| chrX:7209800
|
G | A | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-5+18792G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7209800 | ||||||
| chrX:7210134
|
A | G | 1 | a0001c0001t0002g0212 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-5+19126A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7210134 | ||||||
| chrX:7210310
|
C | T | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.-5+19302C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7210310 | ||||||
| chrX:7210404
|
T | C | 5 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0222others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+19396T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7210404 | ||||||
| chrX:7210408
|
C | T | 1 | a0001c0001t0004g0076 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-5+19400C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7210408 | ||||||
| chrX:7210511
|
TA | T | 1 | a0001c0001t0002g0196 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-5+19509delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7210511 | |||||
| chrX:7210786
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0040 | 2 | NA18964.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-5+19778A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7210786 | ||||||
| chrX:7210909
|
T | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0130 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-5+19901T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7210909 | ||||||
| chrX:7210936
|
A | G | 2 | a0001c0001t0002g0217a0001c0001t0028g0195 | 2 | HG01175.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-5+19928A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7210936 | ||||||
| chrX:7211123
|
A | G | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-5+20115A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7211123 | ||||||
| chrX:7211422
|
T | G | 1 | a0001c0001t0004g0193 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-5+20414T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7211422 | ||||||
| chrX:7211574
|
G | A | 75 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.-5+20566G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7211574 | ||||||
| chrX:7211917
|
CTG | C | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5+20910_-5+20911d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7211917 | ||||||
| chrX:7211958
|
C | A | 1 | a0001c0001t0001g0037 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-5+20950C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7211958 | ||||||
| chrX:7211998
|
T | C | 1 | a0001c0001t0001g0001 | 2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.-5+20990T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7211998 | ||||||
| chrX:7212065
|
C | T | 1 | a0001c0001t0004g0193 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-5+21057C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7212065 | ||||||
| chrX:7212142
|
G | A | 2 | a0001c0001t0003g0115a0001c0001t0009g0120 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-5+21134G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7212142 | ||||||
| chrX:7212691
|
T | C | 2 | a0001c0001t0004g0078a0001c0001t0004g0090 | 2 | NA18945.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.-5+21683T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7212691 | ||||||
| chrX:7212899
|
GT | G | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-5+21894delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7212899 | |||||
| chrX:7212998
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-5+21990A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7212998 | ||||||
| chrX:7213044
|
G | T | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5+22036G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7213044 | ||||||
| chrX:7213107
|
A | AG | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-5+22100dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7213107 | |||||
| chrX:7213275
|
AG | A | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-5+22271delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7213275 | |||||
| chrX:7213459
|
T | TG | 1 | a0001c0001t0002g0187 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-5+22454dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7213459 | |||||
| chrX:7213561
|
AG | A | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-5+22557delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7213561 | |||||
| chrX:7213581
|
G | A | 1 | a0001c0001t0003g0173 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-5+22573G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7213581 | ||||||
| chrX:7213662
|
T | C | 1 | a0001c0001t0003g0107 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-5+22654T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7213662 | ||||||
| chrX:7213806
|
C | CG | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-5+22800dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7213806 | |||||
| chrX:7213848
|
AG | A | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-5+22843delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7213848 | |||||
| chrX:7213975
|
C | T | 30 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(27): Show | 31 | HG00558.hp2 HG01256.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.-5+22967C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7213975 | ||||||
| chrX:7214204
|
G | C | 68 | a0001c0001t0001g0082a0001c0001t0001g0215a0001c0001t0002g0004others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-5+23196G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7214204 | ||||||
| chrX:7214236
|
AT | A | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-5+23234delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7214236 | |||||
| chrX:7214255
|
AG | A | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-5+23253delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7214255 | |||||
| chrX:7214261
|
G | A | 74 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(71): Show | 74 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.-5+23253G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7214261 | ||||||
| chrX:7214262
|
C | A | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-5+23254C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7214262 | ||||||
| chrX:7214268
|
A | G | 1 | a0001c0001t0003g0142 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-5+23260A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7214268 | ||||||
| chrX:7214323
|
C | T | 3 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0069 | 3 | HG02809.hp2 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-5+23315C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7214323 | ||||||
| chrX:7214339
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-5+23331C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7214339 | ||||||
| chrX:7214567
|
T | A | 1 | a0001c0001t0035g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-5+23559T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7214567 | ||||||
| chrX:7214671
|
A | G | 1 | a0001c0001t0039g0079 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-5+23663A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7214671 | ||||||
| chrX:7214908
|
C | CAT | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5+23911_-5+23912d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7214908 | |||||
| chrX:7214917
|
A | G | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.-5+23909A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7214917 | ||||||
| chrX:7214919
|
A | ATG | 1 | a0001c0001t0002g0208 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-5+23923_-5+23924d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7214919 | |||||
| chrX:7214931
|
G | A | 1 | a0001c0001t0023g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-5+23923G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7214931 | ||||||
| chrX:7214933
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0149a0001c0001t0002g0099 | 3 | HG01243.hp1 HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-5+23925A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7214933 | ||||||
| chrX:7214945
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-5+23937A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7214945 | ||||||
| chrX:7214956
|
TATATATA others(18): Show |
T | 1 | a0001c0001t0003g0127 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-5+23957_-5+23981d others(27): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7214956 | |||||
| chrX:7214973
|
TATATATA others(1): Show |
T | 1 | a0001c0001t0003g0119 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-5+23973_-5+23980d others(10): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7214973 | |||||
| chrX:7214975
|
TATATAC | T | 70 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(67): Show | 70 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.-5+23973_-5+23978d others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7214975 | |||||
| chrX:7214981
|
C | T | 1 | a0001c0001t0002g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-5+23973C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7214981 | ||||||
| chrX:7214985
|
T | C | 1 | a0001c0001t0002g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-5+23977T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7214985 | ||||||
| chrX:7214986
|
A | G | 1 | a0001c0001t0002g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-5+23978A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7214986 | ||||||
| chrX:7214988
|
ATACG | A | 1 | a0001c0001t0002g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-5+23983_-5+23986d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7214988 | |||||
| chrX:7214989
|
TAC | T | 5 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG01109.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+23982_-5+23983d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7214989 | ||||||
| chrX:7215010
|
GTA | G | 158 | a0001c0001t0001g0027a0001c0001t0001g0082a0001c0001t0001g0087others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-5+24014_-5+24015d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7215010 | |||||
| chrX:7215014
|
A | G | 1 | a0001c0001t0006g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-5+24006A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7215014 | ||||||
| chrX:7215031
|
GTA | G | 1 | a0001c0001t0005g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-5+24032_-5+24033d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7215031 | |||||
| chrX:7215033
|
A | G | 3 | a0001c0001t0005g0221a0001c0001t0037g0224a0004c0009t0002g0225 | 3 | HG01106.hp1 HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-5+24025A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7215033 | ||||||
| chrX:7215040
|
T | TA | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.-5+24033dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7215040 | |||||
| chrX:7215042
|
C | T | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.-5+24034C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7215042 | ||||||
| chrX:7215042
|
CAT | C | 4 | a0001c0001t0002g0197a0001c0001t0007g0126a0001c0001t0008g0177others(1): Show | 4 | HG00323.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+24042_-5+24043d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7215042 | |||||
| chrX:7215050
|
T | TACGTATA others(13): Show |
1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-5+24058_-5+24077d others(22): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7215050 | |||||
| chrX:7215053
|
G | A | 1 | a0001c0001t0040g0227 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-5+24045G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7215053 | ||||||
| chrX:7215110
|
C | CAT | 25 | a0001c0001t0001g0082a0001c0001t0002g0004a0001c0001t0002g0080others(22): Show | 25 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.-5+24108_-5+24109d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7215110 | |||||
| chrX:7215110
|
CAT | C | 1 | a0001c0001t0001g0073 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-5+24108_-5+24109d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7215110 | |||||
| chrX:7215114
|
T | TATAC | 1 | a0001c0001t0001g0020 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-5+24108_-5+24111d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7215114 | |||||
| chrX:7215116
|
T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | NA18961.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-5+24108T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7215116 | ||||||
| chrX:7215116
|
T | TAC | 2 | a0001c0001t0001g0025a0002c0002t0020g0009 | 2 | HG02257.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-5+24130_-5+24131d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7215116 | |||||
| chrX:7215116
|
T | TATAC | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-5+24109_-5+24110i others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7215116 | |||||
| chrX:7215118
|
C | T | 58 | a0001c0001t0001g0114a0001c0001t0001g0149a0001c0001t0001g0215others(55): Show | 58 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.-5+24110C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7215118 | ||||||
| chrX:7215136
|
C | T | 2 | a0001c0001t0004g0084a0001c0001t0004g0085 | 2 | NA19005.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-5+24128C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7215136 | ||||||
| chrX:7215136
|
CACAT | C | 1 | a0001c0001t0002g0106 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-5+24130_-5+24133d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7215136 | |||||
| chrX:7215138
|
C | CACATATA others(1): Show |
3 | a0001c0001t0005g0221a0001c0001t0037g0224a0004c0009t0002g0225 | 3 | HG01106.hp1 HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-5+24131_-5+24132i others(10): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7215138 | |||||
| chrX:7215138
|
C | CAT | 5 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG01109.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+24148_-5+24149d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7215138 | |||||
| chrX:7215138
|
C | CATAT | 1 | a0001c0001t0002g0194 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-5+24146_-5+24149d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7215138 | |||||
| chrX:7215138
|
C | CATATAT | 8 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0222others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5+24144_-5+24149d others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7215138 | |||||
| chrX:7215138
|
C | CATATATA others(3): Show |
1 | a0001c0001t0023g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-5+24140_-5+24149d others(12): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7215138 | |||||
| chrX:7215138
|
C | T | 27 | a0001c0001t0001g0082a0001c0001t0002g0004a0001c0001t0002g0080others(24): Show | 27 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.-5+24130C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7215138 | ||||||
| chrX:7215138
|
CAT | C | 67 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(64): Show | 67 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.-5+24148_-5+24149d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7215138 | |||||
| chrX:7215140
|
T | C | 11 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0073others(8): Show | 11 | HG01168.hp2 HG01243.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5+24132T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7215140 | ||||||
| chrX:7215183
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064 | 3 | HG02922.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-5+24175G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7215183 | ||||||
| chrX:7215214
|
A | G | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-5+24206A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7215214 | ||||||
| chrX:7215435
|
G | A | 1 | a0001c0001t0001g0031 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-5+24427G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7215435 | ||||||
| chrX:7215558
|
G | A | 1 | a0001c0001t0013g0051 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-5+24550G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7215558 | ||||||
| chrX:7216159
|
AC | A | 2 | a0001c0001t0038g0219a0001c0001t0040g0227 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-5+25152delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7216159 | ||||||
| chrX:7216199
|
A | AC | 1 | a0001c0001t0001g0032 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-5+25196dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7216199 | |||||
| chrX:7216303
|
G | T | 1 | a0001c0001t0005g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-5+25295G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7216303 | ||||||
| chrX:7216529
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-5+25521G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7216529 | ||||||
| chrX:7216760
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-5+25752G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7216760 | ||||||
| chrX:7216824
|
T | C | 1 | a0001c0001t0002g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-5+25816T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7216824 | ||||||
| chrX:7217107
|
G | A | 1 | a0001c0001t0005g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-5+26099G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7217107 | ||||||
| chrX:7217270
|
T | C | 1 | a0001c0001t0002g0106 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-5+26262T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7217270 | ||||||
| chrX:7217366
|
T | C | 29 | a0001c0001t0001g0082a0001c0001t0001g0114a0001c0001t0001g0149others(26): Show | 29 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.-5+26358T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7217366 | ||||||
| chrX:7217489
|
G | A | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-5+26481G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7217489 | ||||||
| chrX:7217600
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-5+26592T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7217600 | ||||||
| chrX:7217638
|
A | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0149 | 2 | HG01243.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-5+26630A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7217638 | ||||||
| chrX:7217699
|
A | G | 1 | a0001c0001t0019g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-5+26691A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7217699 | ||||||
| chrX:7217867
|
T | C | 24 | a0001c0001t0003g0151a0001c0001t0003g0152a0001c0001t0003g0156others(21): Show | 24 | HG00140.hp1 HG00639.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.-5+26859T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7217867 | ||||||
| chrX:7218042
|
C | A | 1 | a0001c0001t0001g0032 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-5+27034C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7218042 | ||||||
| chrX:7218338
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-5+27330T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7218338 | ||||||
| chrX:7219197
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-5+28189C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7219197 | ||||||
| chrX:7219217
|
C | A | 1 | a0001c0001t0003g0127 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-5+28209C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7219217 | ||||||
| chrX:7219609
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(4): Show | 8 | HG02129.hp1 NA18940.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5+28601G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7219609 | ||||||
| chrX:7220025
|
A | G | 75 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.-5+29017A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7220025 | ||||||
| chrX:7220517
|
G | A | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5+29509G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7220517 | ||||||
| chrX:7220543
|
A | AT | 25 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0058others(22): Show | 25 | HG00099.hp1 HG01074.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-5+29558dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7220543 | |||||
| chrX:7220543
|
A | ATT | 6 | a0001c0001t0001g0015a0001c0001t0001g0059a0001c0001t0005g0218others(3): Show | 6 | HG02486.hp1 HG02622.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+29557_-5+29558d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7220543 | |||||
| chrX:7220543
|
AT | A | 66 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0053others(63): Show | 66 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.-5+29558delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7220543 | |||||
| chrX:7220543
|
ATT | A | 2 | a0001c0001t0003g0132a0001c0001t0003g0142 | 2 | HG01257.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.-5+29557_-5+29558d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7220543 | |||||
| chrX:7220612
|
G | A | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-5+29604G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7220612 | ||||||
| chrX:7220673
|
C | T | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5+29665C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7220673 | ||||||
| chrX:7220698
|
G | A | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-5+29690G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7220698 | ||||||
| chrX:7221097
|
A | G | 1 | a0001c0001t0002g0036 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-5+30089A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7221097 | ||||||
| chrX:7221109
|
T | A | 1 | a0001c0001t0003g0151 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-5+30101T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7221109 | ||||||
| chrX:7221139
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-5+30131G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7221139 | ||||||
| chrX:7221456
|
T | G | 158 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-5+30448T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7221456 | ||||||
| chrX:7221885
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-5+30877T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7221885 | ||||||
| chrX:7222528
|
C | CA | 18 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0030others(15): Show | 19 | HG00558.hp1 HG01081.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.-4-30645dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7222528 | |||||
| chrX:7222528
|
C | CAA | 12 | a0001c0001t0002g0105a0001c0001t0003g0167a0001c0001t0004g0075others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.-4-30646_-4-30645d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7222528 | |||||
| chrX:7222528
|
C | CAAA | 66 | a0001c0001t0001g0110a0001c0001t0001g0114a0001c0001t0001g0130others(63): Show | 66 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.-4-30647_-4-30645d others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7222528 | |||||
| chrX:7222528
|
C | CAAAA | 9 | a0001c0001t0001g0087a0001c0001t0003g0109a0001c0001t0003g0111others(6): Show | 9 | HG01123.hp2 HG02004.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4-30648_-4-30645d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7222528 | |||||
| chrX:7222528
|
CA | C | 5 | a0001c0001t0001g0021a0001c0001t0001g0042a0001c0001t0001g0048others(2): Show | 5 | HG01516.hp1 HG02015.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4-30645delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7222528 | |||||
| chrX:7222528
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-30656_-4-30645d others(14): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7222528 | |||||
| chrX:7222716
|
G | A | 1 | a0001c0001t0005g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-4-30480G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7222716 | ||||||
| chrX:7222901
|
A | G | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-4-30295A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7222901 | ||||||
| chrX:7222936
|
A | G | 2 | a0003c0003t0003g0146a0003c0003t0003g0147 | 2 | NA18957.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-4-30260A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7222936 | ||||||
| chrX:7223030
|
AT | A | 1 | a0001c0001t0011g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-4-30165delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7223030 | ||||||
| chrX:7223039
|
AC | A | 3 | a0001c0001t0003g0156a0001c0001t0003g0157a0001c0001t0003g0162 | 3 | HG01261.hp1 HG03017.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-4-30155delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7223039 | |||||
| chrX:7223402
|
A | T | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-4-29794A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7223402 | ||||||
| chrX:7223607
|
G | GT | 6 | a0001c0001t0002g0104a0001c0001t0002g0136a0001c0001t0005g0221others(3): Show | 6 | HG01106.hp1 HG02145.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-29580dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7223607 | |||||
| chrX:7223654
|
A | G | 5 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG01109.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4-29542A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7223654 | ||||||
| chrX:7223659
|
C | T | 1 | a0001c0001t0034g0045 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-4-29537C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7223659 | ||||||
| chrX:7223912
|
C | T | 2 | a0001c0001t0002g0180a0001c0001t0002g0186 | 2 | HG00673.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.-4-29284C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7223912 | ||||||
| chrX:7224317
|
C | A | 8 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0222others(5): Show | 8 | HG01074.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-4-28879C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7224317 | ||||||
| chrX:7224573
|
A | G | 1 | a0001c0001t0002g0197 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-4-28623A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7224573 | ||||||
| chrX:7225397
|
G | T | 1 | a0001c0001t0004g0085 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-4-27799G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7225397 | ||||||
| chrX:7225524
|
G | C | 1 | a0001c0001t0002g0004 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-4-27672G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7225524 | ||||||
| chrX:7225624
|
G | A | 158 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-4-27572G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7225624 | ||||||
| chrX:7226048
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-4-27148G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7226048 | ||||||
| chrX:7226172
|
C | A | 1 | a0001c0001t0003g0124 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-4-27024C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7226172 | ||||||
| chrX:7226489
|
G | A | 68 | a0001c0001t0001g0082a0001c0001t0001g0215a0001c0001t0002g0004others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-4-26707G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7226489 | ||||||
| chrX:7226798
|
GT | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-4-26396delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7226798 | |||||
| chrX:7226951
|
C | T | 8 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0222others(5): Show | 8 | HG01074.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-4-26245C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7226951 | ||||||
| chrX:7226990
|
C | T | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-4-26206C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7226990 | ||||||
| chrX:7227024
|
A | G | 1 | a0001c0001t0040g0227 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-4-26172A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7227024 | ||||||
| chrX:7227363
|
C | T | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-4-25833C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7227363 | ||||||
| chrX:7227448
|
G | GT | 69 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0062others(66): Show | 69 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-4-25733dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7227448 | |||||
| chrX:7227448
|
G | GTT | 1 | a0001c0001t0002g0185 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-4-25734_-4-25733d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7227448 | |||||
| chrX:7227448
|
GT | G | 4 | a0001c0001t0001g0069a0001c0001t0002g0136a0001c0001t0003g0142others(1): Show | 4 | HG02897.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-25733delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7227448 | |||||
| chrX:7227451
|
T | G | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-4-25745T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7227451 | ||||||
| chrX:7227612
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-4-25584G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7227612 | ||||||
| chrX:7227620
|
C | G | 1 | a0001c0001t0001g0025 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-4-25576C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7227620 | ||||||
| chrX:7227663
|
A | G | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-4-25533A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7227663 | ||||||
| chrX:7227828
|
C | G | 1 | a0006c0007t0001g0039 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-4-25368C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7227828 | ||||||
| chrX:7227919
|
G | A | 3 | a0001c0001t0005g0221a0001c0001t0037g0224a0004c0009t0002g0225 | 3 | HG01106.hp1 HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-4-25277G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7227919 | ||||||
| chrX:7227942
|
A | G | 1 | a0001c0001t0033g0191 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-4-25254A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7227942 | ||||||
| chrX:7227961
|
A | G | 1 | a0001c0001t0001g0014 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-4-25235A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7227961 | ||||||
| chrX:7228095
|
G | GT | 1 | a0001c0001t0001g0050 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-4-25092dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7228095 | |||||
| chrX:7228312
|
G | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-4-24884G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7228312 | ||||||
| chrX:7228669
|
T | TA | 1 | a0001c0001t0019g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-4-24526dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7228669 | |||||
| chrX:7228742
|
G | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-4-24454G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7228742 | ||||||
| chrX:7229290
|
G | A | 2 | a0002c0002t0020g0009a0002c0002t0027g0097 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-4-23906G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7229290 | ||||||
| chrX:7229528
|
T | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(225): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.-4-23668T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7229528 | ||||||
| chrX:7229775
|
C | G | 1 | a0002c0002t0020g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-4-23421C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7229775 | ||||||
| chrX:7229971
|
G | A | 26 | a0001c0001t0001g0082a0001c0001t0002g0004a0001c0001t0002g0080others(23): Show | 26 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.-4-23225G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7229971 | ||||||
| chrX:7229995
|
C | T | 1 | a0001c0001t0001g0021 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-4-23201C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7229995 | ||||||
| chrX:7230135
|
G | A | 1 | a0001c0001t0002g0205 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-4-23061G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7230135 | ||||||
| chrX:7230455
|
G | A | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-4-22741G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7230455 | ||||||
| chrX:7230476
|
G | A | 1 | a0001c0001t0005g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-4-22720G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7230476 | ||||||
| chrX:7230503
|
T | C | 5 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0068others(2): Show | 5 | HG02630.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-22693T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7230503 | ||||||
| chrX:7230505
|
G | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0130 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-4-22691G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7230505 | ||||||
| chrX:7230721
|
T | C | 71 | a0001c0001t0001g0082a0001c0001t0001g0114a0001c0001t0001g0149others(68): Show | 71 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.-4-22475T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7230721 | ||||||
| chrX:7231120
|
T | C | 1 | a0001c0001t0002g0212 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-4-22076T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7231120 | ||||||
| chrX:7231795
|
C | T | 1 | a0001c0001t0002g0036 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-4-21401C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7231795 | ||||||
| chrX:7231834
|
C | CT | 81 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(78): Show | 81 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.-4-21345dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7231834 | |||||
| chrX:7231834
|
C | CTT | 1 | a0004c0009t0002g0225 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-4-21346_-4-21345d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7231834 | |||||
| chrX:7231834
|
CT | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(58): Show | 62 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.-4-21345delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7231834 | |||||
| chrX:7231834
|
CTT | C | 2 | a0001c0001t0001g0048a0001c0001t0002g0099 | 2 | HG02622.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-4-21346_-4-21345d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7231834 | |||||
| chrX:7231976
|
A | G | 69 | a0001c0001t0001g0082a0001c0001t0001g0215a0001c0001t0002g0004others(66): Show | 69 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-4-21220A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7231976 | ||||||
| chrX:7232047
|
T | C | 75 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.-4-21149T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7232047 | ||||||
| chrX:7232239
|
C | G | 158 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-4-20957C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7232239 | ||||||
| chrX:7232358
|
A | C | 1 | a0001c0001t0011g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-4-20838A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7232358 | ||||||
| chrX:7232384
|
T | G | 1 | a0001c0001t0003g0148 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-4-20812T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7232384 | ||||||
| chrX:7232456
|
A | G | 75 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.-4-20740A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7232456 | ||||||
| chrX:7232580
|
G | A | 3 | a0001c0001t0002g0080a0001c0001t0002g0094a0001c0001t0002g0098 | 3 | HG02723.hp2 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-4-20616G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7232580 | ||||||
| chrX:7232737
|
A | G | 1 | a0001c0001t0002g0136 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-4-20459A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7232737 | ||||||
| chrX:7232841
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG01192.hp1 HG01361.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-20355G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7232841 | ||||||
| chrX:7233091
|
C | CT | 64 | a0001c0001t0001g0082a0001c0001t0001g0114a0001c0001t0001g0149others(61): Show | 64 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.-4-20085dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7233091 | |||||
| chrX:7233091
|
C | CTT | 2 | a0001c0001t0002g0181a0001c0001t0004g0193 | 2 | HG04115.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-4-20086_-4-20085d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7233091 | |||||
| chrX:7233091
|
CT | C | 73 | a0001c0001t0001g0010a0001c0001t0001g0069a0001c0001t0001g0070others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.-4-20085delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7233091 | |||||
| chrX:7233091
|
CTT | C | 3 | a0001c0001t0003g0119a0001c0001t0003g0142a0001c0001t0003g0172 | 3 | HG03130.hp1 NA18948.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-4-20086_-4-20085d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7233091 | |||||
| chrX:7233097
|
T | C | 1 | a0001c0001t0035g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-4-20099T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7233097 | ||||||
| chrX:7233165
|
C | T | 2 | a0003c0003t0003g0146a0003c0003t0003g0147 | 2 | NA18957.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-4-20031C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7233165 | ||||||
| chrX:7233528
|
G | A | 17 | a0001c0001t0001g0082a0001c0001t0002g0083a0001c0001t0004g0074others(14): Show | 17 | HG00558.hp1 NA18943.hp1 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.-4-19668G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7233528 | ||||||
| chrX:7233548
|
A | G | 30 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(27): Show | 31 | HG00558.hp2 HG01256.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.-4-19648A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7233548 | ||||||
| chrX:7233616
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-4-19580A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7233616 | ||||||
| chrX:7234072
|
G | A | 68 | a0001c0001t0001g0082a0001c0001t0001g0215a0001c0001t0002g0004others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-4-19124G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7234072 | ||||||
| chrX:7234513
|
G | A | 30 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(27): Show | 31 | HG00558.hp2 HG01256.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.-4-18683G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7234513 | ||||||
| chrX:7234534
|
G | T | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-4-18662G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7234534 | ||||||
| chrX:7234581
|
C | T | 9 | a0001c0001t0002g0180a0001c0001t0002g0182a0001c0001t0002g0186others(6): Show | 9 | HG00609.hp1 HG00673.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4-18615C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7234581 | ||||||
| chrX:7234675
|
A | G | 1 | a0001c0001t0002g0203 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-4-18521A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7234675 | ||||||
| chrX:7234877
|
A | G | 1 | a0002c0002t0020g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-4-18319A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7234877 | ||||||
| chrX:7235029
|
C | T | 3 | a0001c0001t0002g0080a0001c0001t0002g0094a0001c0001t0002g0098 | 3 | HG02723.hp2 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-4-18167C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7235029 | ||||||
| chrX:7235416
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-4-17780C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7235416 | ||||||
| chrX:7236587
|
A | C | 1 | a0001c0001t0038g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-4-16609A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7236587 | ||||||
| chrX:7236657
|
CTTAT | C | 75 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.-4-16533_-4-16530d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7236657 | |||||
| chrX:7236812
|
G | A | 75 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.-4-16384G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7236812 | ||||||
| chrX:7236878
|
C | CT | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(225): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.-4-16307dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7236878 | |||||
| chrX:7237056
|
A | G | 11 | a0001c0001t0003g0151a0001c0001t0003g0152a0001c0001t0003g0163others(8): Show | 11 | HG02040.hp1 NA18612.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.-4-16140A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7237056 | ||||||
| chrX:7237105
|
A | G | 3 | a0001c0001t0001g0012a0001c0001t0012g0028a0001c0001t0012g0029 | 3 | HG00642.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-4-16091A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7237105 | ||||||
| chrX:7237213
|
C | CA | 5 | a0001c0001t0009g0120a0001c0001t0021g0096a0001c0001t0039g0079others(2): Show | 5 | HG01169.hp2 HG02257.hp2 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-15968dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7237213 | |||||
| chrX:7237213
|
C | CAA | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.-4-15969_-4-15968d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7237213 | |||||
| chrX:7237213
|
C | CAAA | 13 | a0001c0001t0003g0124a0001c0001t0005g0218a0001c0001t0005g0220others(10): Show | 13 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-4-15970_-4-15968d others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7237213 | |||||
| chrX:7237213
|
CA | C | 4 | a0001c0001t0001g0044a0001c0001t0002g0036a0001c0001t0002g0187others(1): Show | 4 | HG00099.hp2 HG01433.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4-15968delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7237213 | |||||
| chrX:7237642
|
T | C | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-4-15554T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7237642 | ||||||
| chrX:7238121
|
G | GGT | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(29): Show | 34 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.-4-15036_-4-15035d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7238121 | |||||
| chrX:7238121
|
G | GGTGT | 16 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(13): Show | 16 | HG00558.hp2 HG00642.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.-4-15038_-4-15035d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7238121 | |||||
| chrX:7238121
|
G | GGTGTGT | 10 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(7): Show | 10 | HG02071.hp1 HG02257.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-4-15040_-4-15035d others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7238121 | |||||
| chrX:7238121
|
G | GGTGTGTG others(3): Show |
1 | a0001c0001t0001g0017 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-4-15044_-4-15035d others(12): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7238121 | |||||
| chrX:7238121
|
GGT | G | 12 | a0001c0001t0002g0004a0001c0001t0002g0192a0001c0001t0002g0208others(9): Show | 12 | HG00639.hp1 HG01516.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-4-15036_-4-15035d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7238121 | |||||
| chrX:7238121
|
GGTGT | G | 73 | a0001c0001t0001g0082a0001c0001t0001g0215a0001c0001t0002g0083others(70): Show | 73 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.-4-15038_-4-15035d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7238121 | |||||
| chrX:7238121
|
GGTGTGT | G | 67 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(64): Show | 67 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.-4-15040_-4-15035d others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7238121 | |||||
| chrX:7238121
|
GGTGTGTG others(1): Show |
G | 3 | a0001c0001t0002g0080a0001c0001t0002g0094a0001c0001t0003g0166 | 3 | HG02723.hp2 HG02809.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-4-15042_-4-15035d others(10): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7238121 | |||||
| chrX:7238178
|
G | GTAGA | 8 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0070others(5): Show | 8 | HG00639.hp1 HG00741.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-14974_-4-14971d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7238178 | |||||
| chrX:7238178
|
G | GTAGATAG others(1): Show |
2 | a0001c0001t0012g0028a0001c0001t0012g0029 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-4-14978_-4-14971d others(10): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7238178 | |||||
| chrX:7238178
|
GTAGA | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(106): Show | 111 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.-4-14974_-4-14971d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7238178 | |||||
| chrX:7238178
|
GTAGATAG others(1): Show |
G | 10 | a0001c0001t0004g0093a0001c0001t0005g0218a0001c0001t0005g0220others(7): Show | 10 | HG00140.hp1 HG01074.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-4-14978_-4-14971d others(10): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7238178 | |||||
| chrX:7238178
|
GTAGATAG others(5): Show |
G | 6 | a0001c0001t0002g0204a0001c0001t0002g0206a0001c0001t0002g0207others(3): Show | 6 | HG00609.hp1 HG02572.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4-14982_-4-14971d others(14): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7238178 | |||||
| chrX:7238178
|
GTAGATAG others(9): Show |
G | 40 | a0001c0001t0001g0215a0001c0001t0002g0179a0001c0001t0002g0180others(37): Show | 40 | HG00099.hp2 HG00323.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.-4-14986_-4-14971d others(18): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7238178 | |||||
| chrX:7238178
|
GTAGATAG others(13): Show |
G | 1 | a0001c0001t0002g0189 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-4-14990_-4-14971d others(22): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7238178 | |||||
| chrX:7238371
|
C | T | 1 | a0001c0001t0003g0173 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-4-14825C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7238371 | ||||||
| chrX:7238670
|
AT | A | 1 | a0001c0001t0007g0126 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-4-14519delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7238670 | |||||
| chrX:7238677
|
TA | T | 1 | a0001c0001t0003g0167 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-4-14514delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7238677 | |||||
| chrX:7238737
|
CAGG | C | 68 | a0001c0001t0001g0082a0001c0001t0001g0215a0001c0001t0002g0004others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-4-14454_-4-14452d others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7238737 | |||||
| chrX:7238934
|
G | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(6): Show | 10 | HG00621.hp1 HG01081.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.-4-14262G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7238934 | ||||||
| chrX:7239087
|
T | C | 158 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-4-14109T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7239087 | ||||||
| chrX:7239282
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-4-13914C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7239282 | ||||||
| chrX:7239611
|
G | A | 89 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(86): Show | 89 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(86): Show |
intron_variant | MODIFIER | c.-4-13585G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7239611 | ||||||
| chrX:7239630
|
AGTTT | A | 1 | a0001c0001t0011g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-4-13562_-4-13559d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7239630 | |||||
| chrX:7239802
|
G | A | 1 | a0001c0001t0002g0207 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-4-13394G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7239802 | ||||||
| chrX:7239881
|
C | CT | 3 | a0001c0001t0001g0030a0001c0001t0001g0050a0001c0001t0003g0111 | 3 | HG02027.hp1 HG02071.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.-4-13298dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7239881 | |||||
| chrX:7239881
|
CT | C | 139 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0082others(136): Show | 139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-4-13298delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7239881 | |||||
| chrX:7239881
|
CTT | C | 12 | a0001c0001t0002g0099a0001c0001t0005g0218a0001c0001t0005g0220others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-4-13299_-4-13298d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7239881 | |||||
| chrX:7240073
|
A | G | 75 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.-4-13123A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7240073 | ||||||
| chrX:7240076
|
C | T | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-13120C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7240076 | ||||||
| chrX:7240077
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-4-13119G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7240077 | ||||||
| chrX:7240465
|
G | GCA | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | NA18981.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-4-12712_-4-12711d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240465 | |||||
| chrX:7240465
|
GCA | G | 73 | a0001c0001t0001g0087a0001c0001t0001g0114a0001c0001t0001g0149others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.-4-12712_-4-12711d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240465 | |||||
| chrX:7240467
|
A | G | 1 | a0001c0001t0038g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-4-12729A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7240467 | ||||||
| chrX:7240484
|
C | G | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-4-12712C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7240484 | ||||||
| chrX:7240486
|
G | T | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-4-12710G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7240486 | ||||||
| chrX:7240487
|
ATATG | A | 1 | a0002c0002t0020g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-4-12703_-4-12700d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240487 | |||||
| chrX:7240489
|
A | G | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-4-12707A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7240489 | ||||||
| chrX:7240493
|
A | ATG | 1 | a0001c0001t0005g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-4-12663_-4-12662d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240493 | |||||
| chrX:7240493
|
A | G | 2 | a0001c0001t0002g0098a0002c0002t0027g0097 | 2 | HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-4-12703A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7240493 | ||||||
| chrX:7240493
|
ATG | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0061 | 2 | HG00741.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-4-12663_-4-12662d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240493 | |||||
| chrX:7240493
|
ATGTGTGT others(9): Show |
A | 3 | a0001c0001t0001g0110a0001c0001t0001g0130a0001c0001t0003g0163 | 3 | HG02717.hp1 NA18522.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-4-12677_-4-12662d others(18): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240493 | |||||
| chrX:7240493
|
ATGTGTGT others(13): Show |
A | 2 | a0001c0001t0003g0172a0007c0004t0003g0150 | 2 | NA19003.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-4-12681_-4-12662d others(22): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240493 | |||||
| chrX:7240493
|
ATGTGTGT others(15): Show |
A | 55 | a0001c0001t0001g0087a0001c0001t0003g0101a0001c0001t0003g0107others(52): Show | 55 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.-4-12683_-4-12662d others(24): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240493 | |||||
| chrX:7240493
|
ATGTGTGT others(17): Show |
A | 15 | a0001c0001t0001g0114a0001c0001t0001g0149a0001c0001t0002g0104others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.-4-12685_-4-12662d others(26): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240493 | |||||
| chrX:7240507
|
GTGT | G | 1 | a0001c0001t0004g0075 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-4-12688_-4-12686d others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7240507 | ||||||
| chrX:7240525
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0130a0001c0001t0003g0163 | 3 | HG02717.hp1 NA18522.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-4-12671G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7240525 | ||||||
| chrX:7240525
|
GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0025g0202 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-4-12669_-4-12658d others(14): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240525 | |||||
| chrX:7240527
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0130a0001c0001t0003g0163 | 3 | HG02717.hp1 NA18522.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-4-12669G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7240527 | ||||||
| chrX:7240527
|
GTGTGTGT others(1): Show |
G | 1 | a0001c0001t0002g0212 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-4-12667_-4-12660d others(10): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240527 | |||||
| chrX:7240527
|
GTGTGTGT others(3): Show |
G | 8 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0182others(5): Show | 8 | HG00280.hp1 HG00323.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-12667_-4-12658d others(12): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240527 | |||||
| chrX:7240529
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0130a0001c0001t0003g0163 | 3 | HG02717.hp1 NA18522.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-4-12667G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7240529 | ||||||
| chrX:7240529
|
G | GTA | 3 | a0001c0001t0001g0021a0001c0001t0001g0032a0001c0001t0031g0018 | 3 | HG02074.hp1 NA18961.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-4-12666_-4-12665i others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240529 | |||||
| chrX:7240529
|
GTGTGTAT others(1): Show |
G | 52 | a0001c0001t0001g0082a0001c0001t0001g0215a0001c0001t0002g0004others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-4-12665_-4-12658d others(10): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240529 | |||||
| chrX:7240531
|
G | A | 66 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0027others(63): Show | 66 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.-4-12665G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7240531 | ||||||
| chrX:7240531
|
G | GTA | 23 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(20): Show | 24 | HG00621.hp1 HG00642.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-4-12664_-4-12663i others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240531 | |||||
| chrX:7240531
|
G | GTATA | 6 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(3): Show | 7 | HG01361.hp1 HG02129.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4-12664_-4-12663i others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240531 | |||||
| chrX:7240531
|
G | GTATATA | 2 | a0001c0001t0001g0023a0001c0001t0002g0036 | 2 | NA18941.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.-4-12664_-4-12663i others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240531 | |||||
| chrX:7240531
|
GTGTATA | G | 5 | a0001c0001t0002g0094a0001c0001t0002g0206a0001c0001t0002g0208others(2): Show | 5 | HG00609.hp1 HG02738.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-12663_-4-12658d others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240531 | |||||
| chrX:7240531
|
GTGTATAT others(1): Show |
G | 1 | a0001c0001t0002g0184 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-4-12663_-4-12656d others(10): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240531 | |||||
| chrX:7240533
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(119): Show | 124 | HG00140.hp1 HG00621.hp1 HG00639.hp2 others(121): Show |
intron_variant | MODIFIER | c.-4-12663G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7240533 | ||||||
| chrX:7240533
|
G | GTA | 5 | a0001c0001t0001g0022a0001c0001t0001g0043a0001c0001t0001g0048others(2): Show | 5 | HG01192.hp1 HG02109.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-12644_-4-12643d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240533 | |||||
| chrX:7240533
|
G | GTATA | 4 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0050others(1): Show | 4 | HG01515.hp1 HG02071.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-12646_-4-12643d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240533 | |||||
| chrX:7240533
|
G | GTATATA | 1 | a0001c0001t0001g0052 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-4-12648_-4-12643d others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240533 | |||||
| chrX:7240533
|
G | GTGTA | 2 | a0001c0001t0005g0223a0002c0002t0027g0097 | 2 | HG02886.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-4-12662_-4-12661i others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240533 | |||||
| chrX:7240533
|
G | GTGTATA | 3 | a0001c0001t0001g0047a0001c0001t0001g0063a0001c0001t0001g0064 | 3 | HG02976.hp2 HG03195.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.-4-12662_-4-12661i others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240533 | |||||
| chrX:7240533
|
G | GTGTGTAT others(1): Show |
4 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0222others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-12662_-4-12661i others(10): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240533 | |||||
| chrX:7240533
|
G | GTGTGTGT others(1): Show |
1 | a0001c0001t0037g0224 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-4-12662_-4-12661i others(10): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240533 | |||||
| chrX:7240533
|
G | GTGTGTGT others(3): Show |
3 | a0001c0001t0023g0228a0001c0001t0038g0219a0001c0001t0040g0227 | 3 | HG01074.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-4-12662_-4-12661i others(12): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240533 | |||||
| chrX:7240533
|
G | GTGTGTGT others(3): Show |
1 | a0004c0009t0002g0225 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-4-12662_-4-12661i others(12): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240533 | |||||
| chrX:7240533
|
GTATA | G | 1 | a0001c0001t0004g0075 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-4-12646_-4-12643d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7240533 | |||||
| chrX:7240534
|
T | TG | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-4-12662_-4-12661i others(3): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7240534 | ||||||
| chrX:7240535
|
A | G | 2 | a0001c0001t0001g0071a0001c0001t0005g0221 | 2 | HG00099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-4-12661A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7240535 | ||||||
| chrX:7240711
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-4-12485C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7240711 | ||||||
| chrX:7241078
|
A | G | 75 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.-4-12118A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7241078 | ||||||
| chrX:7241133
|
A | C | 75 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.-4-12063A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7241133 | ||||||
| chrX:7241573
|
A | G | 1 | a0001c0001t0019g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-4-11623A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7241573 | ||||||
| chrX:7241599
|
C | T | 3 | a0001c0001t0002g0135a0001c0001t0002g0139a0001c0001t0026g0143 | 3 | HG03516.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-4-11597C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7241599 | ||||||
| chrX:7241931
|
A | AT | 1 | a0001c0001t0001g0054 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-4-11256dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7241931 | |||||
| chrX:7242109
|
C | G | 1 | a0001c0001t0002g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-4-11087C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7242109 | ||||||
| chrX:7242521
|
GC | G | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-10672delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7242521 | |||||
| chrX:7242562
|
TGCACTCC others(3): Show |
T | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-10633_-4-10624d others(12): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7242562 | ||||||
| chrX:7242579
|
GA | G | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-10614delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7242579 | |||||
| chrX:7242594
|
T | C | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-10602T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7242594 | ||||||
| chrX:7242599
|
CA | C | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-10593delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7242599 | |||||
| chrX:7242657
|
CA | C | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-10535delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7242657 | |||||
| chrX:7242680
|
A | AT | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-10514dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7242680 | |||||
| chrX:7242761
|
G | GA | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-10432dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7242761 | |||||
| chrX:7242788
|
C | T | 2 | a0001c0001t0003g0167a0001c0001t0003g0168 | 2 | HG01168.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-4-10408C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7242788 | ||||||
| chrX:7242818
|
G | GT | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-10375dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7242818 | |||||
| chrX:7242836
|
T | TC | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-10358dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7242836 | |||||
| chrX:7242871
|
T | TG | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-10324dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7242871 | |||||
| chrX:7242926
|
T | TG | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-10267dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7242926 | |||||
| chrX:7242985
|
C | CT | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-10208dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7242985 | |||||
| chrX:7243050
|
A | T | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-10146A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7243050 | ||||||
| chrX:7243146
|
T | TA | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-10050_-4-10049i others(3): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7243146 | ||||||
| chrX:7243150
|
A | AG | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-10046_-4-10045i others(3): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7243150 | ||||||
| chrX:7243263
|
A | G | 1 | a0001c0001t0035g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-4-9933A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7243263 | ||||||
| chrX:7243290
|
T | TG | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-9905dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7243290 | |||||
| chrX:7243403
|
C | G | 1 | a0001c0001t0001g0069 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-4-9793C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7243403 | ||||||
| chrX:7243434
|
T | C | 75 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.-4-9762T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7243434 | ||||||
| chrX:7243463
|
A | AT | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-9732dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7243463 | |||||
| chrX:7243503
|
C | T | 1 | a0001c0001t0003g0124 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-4-9693C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7243503 | ||||||
| chrX:7243524
|
C | CA | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-9672_-4-9671ins others(1): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7243524 | ||||||
| chrX:7243537
|
G | GT | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-9659_-4-9658ins others(1): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7243537 | ||||||
| chrX:7243600
|
A | AG | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-9595dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7243600 | |||||
| chrX:7243612
|
T | TA | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-9582dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7243612 | |||||
| chrX:7243724
|
AG | A | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-9470delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7243724 | |||||
| chrX:7243739
|
TG | T | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-9455delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7243739 | |||||
| chrX:7243785
|
TG | T | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-9408delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7243785 | |||||
| chrX:7243821
|
T | TG | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-9372dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7243821 | |||||
| chrX:7243850
|
G | GA | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-9345dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7243850 | |||||
| chrX:7243950
|
TC | T | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-9243delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7243950 | |||||
| chrX:7244043
|
T | TG | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-9150dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7244043 | |||||
| chrX:7244049
|
A | AC | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-9146dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7244049 | |||||
| chrX:7244075
|
AAAG | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064 | 3 | HG02922.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-4-9113_-4-9111del others(3): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7244075 | |||||
| chrX:7244096
|
C | A | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-9100C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7244096 | ||||||
| chrX:7244098
|
A | T | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-9098A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7244098 | ||||||
| chrX:7244099
|
T | G | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-9097T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7244099 | ||||||
| chrX:7244257
|
GA | G | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-8937delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7244257 | |||||
| chrX:7244316
|
T | C | 1 | a0001c0001t0035g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-4-8880T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7244316 | ||||||
| chrX:7244361
|
A | AT | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-8834dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7244361 | |||||
| chrX:7244493
|
A | AT | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-8703_-4-8702ins others(1): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7244493 | ||||||
| chrX:7244672
|
G | GA | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-8524_-4-8523ins others(1): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7244672 | ||||||
| chrX:7244688
|
CG | C | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-8504delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7244688 | |||||
| chrX:7244710
|
AG | A | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-8483delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7244710 | |||||
| chrX:7244814
|
T | TA | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-8380dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7244814 | |||||
| chrX:7244891
|
G | A | 1 | a0001c0001t0005g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-4-8305G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7244891 | ||||||
| chrX:7244947
|
C | CA | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-8243dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7244947 | |||||
| chrX:7244990
|
T | TC | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-8204dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7244990 | |||||
| chrX:7245006
|
A | AC | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-8189dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7245006 | |||||
| chrX:7245049
|
T | TG | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-8145dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7245049 | |||||
| chrX:7245121
|
C | CT | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-8071dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7245121 | |||||
| chrX:7245163
|
T | TA | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-8030dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7245163 | |||||
| chrX:7245189
|
T | TC | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-8005dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7245189 | |||||
| chrX:7245214
|
T | TAA | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-7982_-4-7981ins others(2): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7245214 | ||||||
| chrX:7245266
|
C | T | 2 | a0001c0001t0008g0177a0001c0001t0008g0178 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-4-7930C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7245266 | ||||||
| chrX:7245327
|
AT | A | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-7866delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7245327 | |||||
| chrX:7245383
|
AG | A | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-7810delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7245383 | |||||
| chrX:7245535
|
CA | C | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-7660delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7245535 | ||||||
| chrX:7245554
|
T | C | 1 | a0001c0001t0030g0038 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-4-7642T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7245554 | ||||||
| chrX:7245715
|
A | T | 1 | a0001c0001t0001g0050 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-4-7481A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7245715 | ||||||
| chrX:7245727
|
G | T | 1 | a0001c0001t0003g0174 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-4-7469G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7245727 | ||||||
| chrX:7245759
|
C | G | 1 | a0004c0009t0002g0225 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-4-7437C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7245759 | ||||||
| chrX:7245769
|
AG | A | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-7425delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7245769 | |||||
| chrX:7245789
|
C | CCT | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-7407_-4-7406ins others(2): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7245789 | ||||||
| chrX:7245790
|
T | A | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-7406T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7245790 | ||||||
| chrX:7245833
|
C | T | 1 | a0001c0001t0034g0045 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-4-7363C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7245833 | ||||||
| chrX:7245839
|
C | CA | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-7354dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7245839 | |||||
| chrX:7245886
|
C | CTCCAATA others(5): Show |
1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-7305_-4-7294dup others(12): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7245886 | |||||
| chrX:7246048
|
A | AT | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-7145dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7246048 | |||||
| chrX:7246100
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0149a0001c0001t0002g0099 | 3 | HG01243.hp1 HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-4-7096A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7246100 | ||||||
| chrX:7246122
|
A | G | 1 | a0001c0001t0004g0193 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-4-7074A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7246122 | ||||||
| chrX:7246262
|
C | CT | 2 | a0001c0001t0001g0049a0001c0001t0002g0098 | 2 | HG03139.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-4-6917dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7246262 | |||||
| chrX:7246262
|
CT | C | 15 | a0001c0001t0001g0087a0001c0001t0005g0218a0001c0001t0005g0220others(12): Show | 15 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-4-6917delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7246262 | |||||
| chrX:7246284
|
C | T | 1 | a0004c0009t0002g0225 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-4-6912C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7246284 | ||||||
| chrX:7246293
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-4-6903G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7246293 | ||||||
| chrX:7246341
|
G | A | 2 | a0001c0001t0002g0080a0001c0001t0002g0094 | 2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-4-6855G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7246341 | ||||||
| chrX:7246426
|
C | T | 26 | a0001c0001t0001g0082a0001c0001t0002g0004a0001c0001t0002g0080others(23): Show | 26 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.-4-6770C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7246426 | ||||||
| chrX:7246468
|
A | AT | 142 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(139): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.-4-6717dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7246468 | |||||
| chrX:7246468
|
A | ATT | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-4-6718_-4-6717dup others(2): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7246468 | |||||
| chrX:7246474
|
T | TG | 13 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(10): Show | 13 | HG02055.hp1 HG02559.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.-4-6722_-4-6721ins others(1): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7246474 | ||||||
| chrX:7246527
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-4-6669C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7246527 | ||||||
| chrX:7246585
|
C | CT | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-6611_-4-6610ins others(1): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7246585 | ||||||
| chrX:7246597
|
C | T | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.-4-6599C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7246597 | ||||||
| chrX:7246600
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-4-6596C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7246600 | ||||||
| chrX:7246601
|
C | T | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-4-6595C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7246601 | ||||||
| chrX:7246612
|
G | A | 1 | a0001c0001t0002g0217 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-4-6584G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7246612 | ||||||
| chrX:7247065
|
G | GT | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-6127dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7247065 | |||||
| chrX:7247086
|
T | TG | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-4-6110_-4-6109ins others(1): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7247086 | ||||||
| chrX:7247150
|
T | C | 158 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-4-6046T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7247150 | ||||||
| chrX:7247438
|
TA | T | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-4-5752delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7247438 | |||||
| chrX:7247450
|
T | C | 42 | a0001c0001t0001g0215a0001c0001t0002g0179a0001c0001t0002g0180others(39): Show | 42 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.-4-5746T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7247450 | ||||||
| chrX:7247488
|
C | CT | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-5708_-4-5707ins others(1): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7247488 | ||||||
| chrX:7247833
|
C | G | 1 | a0001c0001t0002g0106 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-4-5363C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7247833 | ||||||
| chrX:7248073
|
CA | C | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-4-5116delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7248073 | |||||
| chrX:7248136
|
A | AT | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-5057dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7248136 | |||||
| chrX:7248136
|
AT | A | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-4-5057delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7248136 | |||||
| chrX:7248171
|
C | A | 69 | a0001c0001t0001g0082a0001c0001t0001g0215a0001c0001t0002g0004others(66): Show | 69 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-4-5025C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7248171 | ||||||
| chrX:7248439
|
A | T | 1 | a0001c0001t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-4-4757A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7248439 | ||||||
| chrX:7248504
|
T | TG | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-4690dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7248504 | |||||
| chrX:7248672
|
T | TCTTAA | 157 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(154): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-4-4521_-4-4520ins others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7248672 | |||||
| chrX:7248830
|
ACTG | A | 1 | a0001c0001t0002g0004 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-4-4365_-4-4363del others(3): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7248830 | ||||||
| chrX:7248890
|
TA | T | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-4-4298delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7248890 | |||||
| chrX:7248937
|
A | AT | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-4254dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7248937 | |||||
| chrX:7248994
|
GC | G | 1 | a0001c0001t0001g0024 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-4-4199delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7248994 | |||||
| chrX:7249080
|
T | TA | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-4110dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7249080 | |||||
| chrX:7249137
|
C | T | 1 | a0001c0001t0031g0018 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-4-4059C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7249137 | ||||||
| chrX:7249475
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-4-3721G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7249475 | ||||||
| chrX:7249543
|
C | T | 68 | a0001c0001t0001g0082a0001c0001t0001g0215a0001c0001t0002g0004others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-4-3653C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7249543 | ||||||
| chrX:7249559
|
AT | A | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-4-3635delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7249559 | |||||
| chrX:7249989
|
G | A | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-4-3207G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7249989 | ||||||
| chrX:7250260
|
A | G | 1 | a0006c0007t0001g0039 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-4-2936A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7250260 | ||||||
| chrX:7250403
|
T | TA | 3 | a0001c0001t0001g0040a0001c0001t0005g0220a0001c0001t0041g0003 | 3 | HG02109.hp1 NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.-4-2781dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7250403 | |||||
| chrX:7250403
|
T | TAAAA | 2 | a0001c0001t0001g0114a0001c0001t0001g0149 | 2 | HG01243.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-4-2784_-4-2781dup others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7250403 | |||||
| chrX:7250415
|
AG | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0048a0001c0001t0002g0187others(4): Show | 7 | HG00099.hp2 HG03490.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4-2780delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7250415 | ||||||
| chrX:7250416
|
G | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(211): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.-4-2780G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7250416 | ||||||
| chrX:7250480
|
C | T | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-4-2716C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7250480 | ||||||
| chrX:7250498
|
T | C | 158 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-4-2698T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7250498 | ||||||
| chrX:7250557
|
A | AG | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-4-2638dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7250557 | |||||
| chrX:7250600
|
T | TA | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.-4-2595dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 7250600 | |||||
| chrX:7250647
|
G | A | 1 | a0001c0001t0003g0128 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-4-2549G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7250647 | ||||||
| chrX:7251179
|
C | T | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-4-2017C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7251179 | ||||||
| chrX:7251477
|
T | C | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.-4-1719T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7251477 | ||||||
| chrX:7251505
|
G | T | 5 | a0001c0001t0006g0158a0001c0001t0006g0160a0001c0001t0006g0161others(2): Show | 5 | HG00639.hp2 HG02004.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-1691G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7251505 | ||||||
| chrX:7251609
|
A | C | 9 | a0001c0001t0002g0180a0001c0001t0002g0182a0001c0001t0002g0186others(6): Show | 9 | HG00609.hp1 HG00673.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4-1587A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7251609 | ||||||
| chrX:7251727
|
G | A | 2 | a0002c0002t0020g0009a0002c0002t0027g0097 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-4-1469G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7251727 | ||||||
| chrX:7252884
|
C | G | 158 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-4-312C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 2/10 | chrX | 7252884 | ||||||
| chrX:7253428
|
T | C | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.137+92T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | chrX | 7253428 | ||||||
| chrX:7253514
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0024 | 2 | NA18988.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.137+178T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | chrX | 7253514 | ||||||
| chrX:7253755
|
T | C | 1 | a0001c0001t0035g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.137+419T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | chrX | 7253755 | ||||||
| chrX:7253944
|
G | C | 1 | a0001c0001t0002g0184 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.137+608G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | chrX | 7253944 | ||||||
| chrX:7254129
|
A | G | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.137+793A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | chrX | 7254129 | ||||||
| chrX:7254320
|
C | G | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.137+984C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | chrX | 7254320 | ||||||
| chrX:7254363
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.137+1027C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | chrX | 7254363 | ||||||
| chrX:7254467
|
T | C | 70 | a0001c0001t0001g0082a0001c0001t0001g0215a0001c0001t0002g0004others(67): Show | 70 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.137+1131T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | chrX | 7254467 | ||||||
| chrX:7254577
|
C | CT | 8 | a0001c0001t0001g0042a0001c0001t0002g0179a0001c0001t0003g0166others(5): Show | 8 | HG00639.hp1 HG02015.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.137+1263dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 7254577 | |||||
| chrX:7254577
|
C | CTT | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.137+1262_137+1263d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 7254577 | |||||
| chrX:7254577
|
CT | C | 21 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0032others(18): Show | 21 | HG01943.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.137+1263delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 7254577 | |||||
| chrX:7254841
|
C | A | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.137+1505C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | chrX | 7254841 | ||||||
| chrX:7254844
|
A | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0149 | 2 | HG01243.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.137+1508A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | chrX | 7254844 | ||||||
| chrX:7255879
|
G | T | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.138-1363G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | chrX | 7255879 | ||||||
| chrX:7256024
|
T | A | 1 | a0001c0001t0002g0190 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.138-1218T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | chrX | 7256024 | ||||||
| chrX:7256094
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.138-1148A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | chrX | 7256094 | ||||||
| chrX:7256158
|
G | A | 5 | a0001c0001t0002g0184a0001c0001t0002g0187a0001c0001t0002g0214others(2): Show | 5 | HG00099.hp2 HG01123.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-1084G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | chrX | 7256158 | ||||||
| chrX:7256372
|
C | T | 1 | a0001c0001t0038g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138-870C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | chrX | 7256372 | ||||||
| chrX:7256772
|
G | A | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.138-470G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | chrX | 7256772 | ||||||
| chrX:7256780
|
C | T | 1 | a0006c0007t0001g0039 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.138-462C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 3/10 | chrX | 7256780 | ||||||
| chrX:7257801
|
A | ATG | 2 | a0001c0001t0012g0028a0001c0001t0012g0029 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.382+231_382+232dup others(2): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7257801 | |||||
| chrX:7257801
|
ATG | A | 2 | a0001c0001t0001g0071a0002c0002t0027g0097 | 2 | HG00099.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.382+231_382+232del others(2): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7257801 | |||||
| chrX:7257801
|
ATGTG | A | 1 | a0001c0001t0023g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.382+229_382+232del others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7257801 | |||||
| chrX:7257828
|
TTG | T | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.382+253_382+254del others(2): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7257828 | |||||
| chrX:7258009
|
G | GGGAT | 1 | a0001c0001t0011g0026 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.382+453_382+456dup others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258009 | |||||
| chrX:7258009
|
GGGAT | G | 140 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0114others(137): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.382+453_382+456del others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258009 | |||||
| chrX:7258009
|
GGGATGGA others(1): Show |
G | 1 | a0001c0001t0001g0110 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.382+449_382+456del others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258009 | |||||
| chrX:7258056
|
ATAGCTAG others(1): Show |
A | 1 | a0001c0001t0003g0174 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.382+484_382+491del others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258056 | |||||
| chrX:7258068
|
C | A | 1 | a0001c0001t0001g0052 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.382+480C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | chrX | 7258068 | ||||||
| chrX:7258076
|
C | A | 2 | a0001c0001t0001g0010a0001c0001t0019g0103 | 2 | HG01515.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.382+488C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | chrX | 7258076 | ||||||
| chrX:7258105
|
C | CATAG | 43 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(40): Show | 44 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.382+556_382+559dup others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258105 | |||||
| chrX:7258105
|
C | CATAGATA others(1): Show |
16 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0016others(13): Show | 17 | HG01081.hp2 HG01099.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.382+552_382+559dup others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258105 | |||||
| chrX:7258105
|
C | CATAGATA others(5): Show |
1 | a0001c0001t0001g0022 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.382+548_382+559dup others(12): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258105 | |||||
| chrX:7258105
|
CATAG | C | 15 | a0001c0001t0001g0110a0001c0001t0001g0130a0001c0001t0002g0105others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.382+556_382+559del others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258105 | |||||
| chrX:7258105
|
CATAGATA others(1): Show |
C | 52 | a0001c0001t0002g0099a0001c0001t0002g0144a0001c0001t0002g0197others(49): Show | 52 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.382+552_382+559del others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258105 | |||||
| chrX:7258105
|
CATAGATA others(5): Show |
C | 74 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0114others(71): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.382+548_382+559del others(12): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258105 | |||||
| chrX:7258105
|
CATAGATA others(9): Show |
C | 1 | a0001c0001t0036g0006 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.382+544_382+559del others(16): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258105 | |||||
| chrX:7258105
|
CATAGATA others(13): Show |
C | 2 | a0001c0001t0002g0183a0001c0001t0002g0185 | 2 | NA19066.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.382+540_382+559del others(20): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258105 | |||||
| chrX:7258166
|
GAGAT | G | 5 | a0001c0001t0005g0138a0001c0001t0005g0218a0001c0001t0005g0220others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.382+595_382+598del others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258166 | |||||
| chrX:7258267
|
G | GGATA | 52 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(49): Show | 52 | HG00140.hp1 HG00639.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.382+707_382+710dup others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258267 | |||||
| chrX:7258267
|
G | GGATAGAT others(1): Show |
9 | a0001c0001t0002g0135a0001c0001t0003g0115a0001c0001t0003g0123others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.382+703_382+710dup others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258267 | |||||
| chrX:7258267
|
G | GGATAGAT others(5): Show |
1 | a0001c0001t0003g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.382+699_382+710dup others(12): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258267 | |||||
| chrX:7258267
|
G | GGATAGAT others(9): Show |
1 | a0001c0001t0003g0151 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.382+695_382+710dup others(16): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258267 | |||||
| chrX:7258267
|
GGATA | G | 1 | a0001c0001t0003g0157 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.382+707_382+710del others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258267 | |||||
| chrX:7258346
|
GGATA | G | 10 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(7): Show | 10 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.382+767_382+770del others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258346 | |||||
| chrX:7258413
|
C | T | 75 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.382+825C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | chrX | 7258413 | ||||||
| chrX:7258421
|
TAGAA | T | 1 | a0001c0001t0001g0055 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.382+838_382+841del others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258421 | |||||
| chrX:7258532
|
T | TA | 1 | a0001c0001t0002g0182 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.383-816dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258532 | |||||
| chrX:7258821
|
T | TG | 1 | a0001c0001t0003g0108 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.383-528_383-527ins others(1): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | chrX | 7258821 | ||||||
| chrX:7258907
|
G | GA | 75 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.383-429dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258907 | |||||
| chrX:7258907
|
GA | G | 2 | a0001c0001t0002g0182a0001c0001t0002g0200 | 2 | HG02257.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.383-429delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7258907 | |||||
| chrX:7259158
|
G | A | 1 | a0001c0001t0002g0139 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.383-191G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | chrX | 7259158 | ||||||
| chrX:7259254
|
A | G | 1 | a0002c0002t0020g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.383-95A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | chrX | 7259254 | ||||||
| chrX:7259297
|
TG | T | 1 | a0001c0001t0003g0108 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.383-50delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 7259297 | |||||
| chrX:7259333
|
C | T | 1 | a0001c0001t0003g0167 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.383-16C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 5/10 | chrX | 7259333 | ||||||
| chrX:7259937
|
G | A | 69 | a0001c0001t0001g0082a0001c0001t0001g0215a0001c0001t0002g0004others(66): Show | 69 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.806+165G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7259937 | ||||||
| chrX:7259986
|
C | T | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.806+214C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7259986 | ||||||
| chrX:7260016
|
T | C | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.806+244T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7260016 | ||||||
| chrX:7260024
|
C | T | 2 | a0001c0001t0038g0219a0001c0001t0040g0227 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.806+252C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7260024 | ||||||
| chrX:7260352
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.806+580G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7260352 | ||||||
| chrX:7260751
|
A | T | 2 | a0001c0001t0004g0084a0001c0001t0004g0085 | 2 | NA19005.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.806+979A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7260751 | ||||||
| chrX:7261047
|
G | A | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.806+1275G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7261047 | ||||||
| chrX:7262045
|
C | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0130 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.806+2273C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7262045 | ||||||
| chrX:7262075
|
A | G | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.806+2303A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7262075 | ||||||
| chrX:7262169
|
A | C | 4 | a0001c0001t0002g0197a0001c0001t0007g0126a0001c0001t0008g0177others(1): Show | 4 | HG00323.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.806+2397A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7262169 | ||||||
| chrX:7262489
|
G | T | 74 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(71): Show | 74 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.806+2717G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7262489 | ||||||
| chrX:7262505
|
T | G | 1 | a0001c0001t0005g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.806+2733T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7262505 | ||||||
| chrX:7262546
|
G | T | 1 | a0001c0001t0001g0042 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.806+2774G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7262546 | ||||||
| chrX:7263038
|
A | G | 75 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.806+3266A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7263038 | ||||||
| chrX:7263100
|
G | A | 1 | a0004c0009t0002g0225 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.806+3328G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7263100 | ||||||
| chrX:7263215
|
T | C | 87 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(84): Show | 87 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(84): Show |
intron_variant | MODIFIER | c.806+3443T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7263215 | ||||||
| chrX:7263361
|
G | A | 2 | a0001c0001t0003g0115a0001c0001t0009g0120 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.806+3589G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7263361 | ||||||
| chrX:7263412
|
A | T | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.806+3640A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7263412 | ||||||
| chrX:7263431
|
T | C | 2 | a0002c0002t0020g0009a0002c0002t0027g0097 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.806+3659T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7263431 | ||||||
| chrX:7263564
|
G | A | 5 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG01109.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.806+3792G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7263564 | ||||||
| chrX:7263829
|
ATG | A | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.806+4068_806+4069d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7263829 | |||||
| chrX:7263918
|
T | A | 1 | a0001c0001t0001g0087 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.806+4146T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7263918 | ||||||
| chrX:7264134
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.806+4362G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7264134 | ||||||
| chrX:7264242
|
C | A | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.806+4470C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7264242 | ||||||
| chrX:7264451
|
G | A | 26 | a0001c0001t0001g0082a0001c0001t0002g0004a0001c0001t0002g0080others(23): Show | 26 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.806+4679G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7264451 | ||||||
| chrX:7264577
|
A | AG | 1 | a0001c0001t0002g0189 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.806+4809dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7264577 | |||||
| chrX:7264728
|
A | T | 1 | a0001c0001t0002g0212 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.806+4956A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7264728 | ||||||
| chrX:7265022
|
G | GT | 8 | a0001c0001t0002g0099a0001c0001t0002g0179a0001c0001t0002g0196others(5): Show | 8 | HG01952.hp1 HG02622.hp2 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.806+5266dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7265022 | |||||
| chrX:7265022
|
GT | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(147): Show | 152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.806+5266delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7265022 | |||||
| chrX:7265022
|
GTT | G | 6 | a0001c0001t0001g0031a0001c0001t0001g0064a0001c0001t0003g0163others(3): Show | 6 | HG02040.hp1 HG02976.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.806+5265_806+5266d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7265022 | |||||
| chrX:7265069
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.806+5297T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7265069 | ||||||
| chrX:7265188
|
G | C | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.806+5416G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7265188 | ||||||
| chrX:7265890
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0149 | 2 | HG01243.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.806+6118C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7265890 | ||||||
| chrX:7266174
|
CAT | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(183): Show | 188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.806+6415_806+6416d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7266174 | |||||
| chrX:7266574
|
G | A | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.806+6802G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7266574 | ||||||
| chrX:7266593
|
A | G | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.806+6821A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7266593 | ||||||
| chrX:7267086
|
A | G | 87 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(84): Show | 87 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(84): Show |
intron_variant | MODIFIER | c.806+7314A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7267086 | ||||||
| chrX:7267427
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0149a0001c0001t0002g0099 | 3 | HG01243.hp1 HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.806+7655A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7267427 | ||||||
| chrX:7267758
|
A | G | 1 | a0001c0001t0003g0109 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.806+7986A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7267758 | ||||||
| chrX:7267813
|
A | G | 9 | a0001c0001t0003g0101a0001c0001t0003g0109a0001c0001t0003g0113others(6): Show | 9 | HG00738.hp1 HG01081.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.806+8041A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7267813 | ||||||
| chrX:7268036
|
C | T | 5 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG01109.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.807-7915C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7268036 | ||||||
| chrX:7268193
|
C | G | 14 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(11): Show | 14 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.807-7758C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7268193 | ||||||
| chrX:7268494
|
AAG | A | 2 | a0001c0001t0002g0187a0001c0001t0002g0214 | 2 | HG00099.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.807-7454_807-7453d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7268494 | |||||
| chrX:7268624
|
ATAAT | A | 1 | a0001c0001t0002g0139 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.807-7323_807-7320d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7268624 | |||||
| chrX:7268815
|
C | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(67): Show | 72 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.807-7136C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7268815 | ||||||
| chrX:7268985
|
C | CA | 1 | a0001c0001t0003g0122 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.807-6960dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7268985 | |||||
| chrX:7269023
|
C | T | 2 | a0001c0001t0002g0183a0001c0001t0002g0185 | 2 | NA19066.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.807-6928C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7269023 | ||||||
| chrX:7269466
|
A | C | 1 | a0001c0001t0002g0194 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.807-6485A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7269466 | ||||||
| chrX:7269738
|
G | A | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.807-6213G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7269738 | ||||||
| chrX:7269751
|
T | C | 75 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.807-6200T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7269751 | ||||||
| chrX:7269778
|
A | G | 8 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0071others(5): Show | 8 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.807-6173A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7269778 | ||||||
| chrX:7269851
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.807-6100C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7269851 | ||||||
| chrX:7270118
|
G | A | 1 | a0001c0001t0002g0194 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.807-5833G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7270118 | ||||||
| chrX:7270186
|
C | T | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.807-5765C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7270186 | ||||||
| chrX:7270998
|
C | CT | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.807-4940dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7270998 | |||||
| chrX:7270998
|
CT | C | 4 | a0001c0001t0001g0023a0001c0001t0004g0077a0001c0001t0004g0198others(1): Show | 4 | HG00558.hp1 HG01256.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.807-4940delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7270998 | |||||
| chrX:7271000
|
T | TC | 1 | a0001c0001t0003g0157 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.807-4951_807-4950i others(3): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7271000 | ||||||
| chrX:7271576
|
A | T | 1 | a0001c0001t0001g0044 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.807-4375A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7271576 | ||||||
| chrX:7271719
|
A | AT | 6 | a0001c0001t0002g0139a0001c0001t0002g0196a0001c0001t0003g0122others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.807-4218dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7271719 | |||||
| chrX:7271719
|
AT | A | 5 | a0001c0001t0002g0135a0001c0001t0004g0198a0001c0001t0008g0177others(2): Show | 5 | HG01169.hp1 HG02976.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.807-4218delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7271719 | |||||
| chrX:7271740
|
C | T | 8 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0222others(5): Show | 8 | HG01074.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.807-4211C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7271740 | ||||||
| chrX:7271785
|
T | TA | 2 | a0001c0001t0003g0107a0001c0001t0014g0216 | 2 | HG02083.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.807-4153dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7271785 | |||||
| chrX:7271901
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.807-4050C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7271901 | ||||||
| chrX:7272030
|
T | C | 1 | a0001c0001t0037g0224 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.807-3921T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7272030 | ||||||
| chrX:7272079
|
G | C | 2 | a0001c0001t0004g0078a0001c0001t0004g0090 | 2 | NA18945.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.807-3872G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7272079 | ||||||
| chrX:7272217
|
C | CAT | 1 | a0001c0001t0003g0172 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.807-3717_807-3716d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7272217 | |||||
| chrX:7272217
|
C | CATAT | 70 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(67): Show | 70 | HG00140.hp1 HG00738.hp1 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.807-3719_807-3716d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7272217 | |||||
| chrX:7272217
|
C | CATATAT | 39 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(36): Show | 39 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.807-3721_807-3716d others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7272217 | |||||
| chrX:7272217
|
C | CATATATA others(1): Show |
11 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0063others(8): Show | 11 | HG00099.hp1 HG01243.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.807-3723_807-3716d others(10): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7272217 | |||||
| chrX:7272217
|
C | CATATATA others(3): Show |
21 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(18): Show | 22 | HG01081.hp2 HG01099.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.807-3725_807-3716d others(12): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7272217 | |||||
| chrX:7272217
|
C | CATATATA others(5): Show |
32 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(29): Show | 33 | HG00558.hp2 HG00621.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.807-3727_807-3716d others(14): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7272217 | |||||
| chrX:7272217
|
C | CATATATA others(7): Show |
7 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0024others(4): Show | 7 | HG01074.hp1 HG03098.hp1 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.807-3729_807-3716d others(16): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7272217 | |||||
| chrX:7272217
|
C | CATATATA others(9): Show |
2 | a0001c0001t0001g0012a0001c0001t0001g0031 | 2 | HG00642.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.807-3731_807-3716d others(18): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7272217 | |||||
| chrX:7272217
|
C | CATATATA others(11): Show |
2 | a0001c0001t0001g0050a0006c0007t0001g0039 | 2 | HG02071.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.807-3733_807-3716d others(20): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7272217 | |||||
| chrX:7272217
|
CAT | C | 1 | a0001c0001t0003g0107 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.807-3717_807-3716d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7272217 | |||||
| chrX:7272296
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.807-3655A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7272296 | ||||||
| chrX:7272682
|
A | C | 1 | a0001c0001t0002g0201 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.807-3269A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7272682 | ||||||
| chrX:7273114
|
C | T | 1 | a0001c0001t0028g0195 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.807-2837C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7273114 | ||||||
| chrX:7273145
|
A | G | 75 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.807-2806A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7273145 | ||||||
| chrX:7273481
|
C | T | 2 | a0001c0001t0007g0153a0001c0001t0007g0154 | 2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.807-2470C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7273481 | ||||||
| chrX:7273592
|
C | T | 1 | a0001c0001t0005g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.807-2359C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7273592 | ||||||
| chrX:7273593
|
G | A | 1 | a0001c0001t0035g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.807-2358G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7273593 | ||||||
| chrX:7273779
|
T | TA | 2 | a0001c0001t0002g0105a0001c0001t0002g0207 | 2 | HG02922.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.807-2162dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7273779 | |||||
| chrX:7273779
|
TAAAAAA | T | 1 | a0001c0001t0002g0106 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.807-2167_807-2162d others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7273779 | |||||
| chrX:7274121
|
CTG | C | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.807-1825_807-1824d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7274121 | |||||
| chrX:7274124
|
T | G | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.807-1827T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7274124 | ||||||
| chrX:7274660
|
A | C | 2 | a0002c0002t0020g0009a0002c0002t0027g0097 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.807-1291A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7274660 | ||||||
| chrX:7274767
|
C | T | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.807-1184C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7274767 | ||||||
| chrX:7275389
|
G | A | 3 | a0001c0001t0002g0144a0001c0001t0010g0100a0001c0001t0010g0145 | 3 | HG02055.hp1 HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.807-562G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7275389 | ||||||
| chrX:7275514
|
T | C | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.807-437T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7275514 | ||||||
| chrX:7275544
|
G | C | 1 | a0001c0001t0001g0027 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.807-407G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7275544 | ||||||
| chrX:7275559
|
T | C | 1 | a0001c0001t0009g0170 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.807-392T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | chrX | 7275559 | ||||||
| chrX:7275929
|
C | CT | 10 | a0001c0001t0001g0022a0001c0001t0002g0181a0001c0001t0002g0185others(7): Show | 10 | HG01168.hp2 HG01358.hp1 HG01516.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.807-5dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7275929 | |||||
| chrX:7275929
|
CT | C | 3 | a0001c0001t0001g0046a0001c0001t0006g0160a0001c0001t0006g0176 | 3 | HG02735.hp1 NA18999.hp1 NA20805.hp1 |
splice_region_variant&intron_variant | LOW | c.807-5delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 7275929 | |||||
| chrX:7276187
|
A | C | 1 | a0001c0001t0002g0139 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.943+100A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7276187 | ||||||
| chrX:7276477
|
A | T | 1 | a0001c0001t0007g0154 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.943+390A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7276477 | ||||||
| chrX:7276488
|
C | A | 1 | a0001c0001t0002g0203 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.943+401C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7276488 | ||||||
| chrX:7276736
|
C | T | 1 | a0001c0001t0002g0213 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.943+649C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7276736 | ||||||
| chrX:7276742
|
C | G | 1 | a0002c0002t0020g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.943+655C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7276742 | ||||||
| chrX:7276950
|
T | A | 1 | a0001c0001t0002g0212 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.943+863T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7276950 | ||||||
| chrX:7277065
|
T | G | 1 | a0001c0001t0003g0175 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.943+978T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7277065 | ||||||
| chrX:7277626
|
A | G | 1 | a0001c0001t0003g0171 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.943+1539A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7277626 | ||||||
| chrX:7277632
|
G | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0130 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.943+1545G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7277632 | ||||||
| chrX:7277761
|
C | T | 7 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0035others(4): Show | 7 | HG02015.hp1 NA18982.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.943+1674C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7277761 | ||||||
| chrX:7277851
|
C | T | 1 | a0002c0002t0020g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.943+1764C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7277851 | ||||||
| chrX:7277902
|
AT | A | 1 | a0001c0001t0002g0189 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.943+1819delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7277902 | |||||
| chrX:7278113
|
T | A | 1 | a0001c0001t0002g0189 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.943+2026T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7278113 | ||||||
| chrX:7278114
|
A | G | 1 | a0001c0001t0002g0189 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.943+2027A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7278114 | ||||||
| chrX:7278115
|
G | C | 1 | a0001c0001t0002g0189 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.943+2028G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7278115 | ||||||
| chrX:7278552
|
G | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.943+2465G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7278552 | ||||||
| chrX:7278848
|
C | T | 2 | a0001c0001t0002g0180a0001c0001t0002g0186 | 2 | HG00673.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.943+2761C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7278848 | ||||||
| chrX:7279161
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.943+3074G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279161 | ||||||
| chrX:7279173
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.943+3086G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279173 | ||||||
| chrX:7279279
|
G | GA | 8 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0135others(5): Show | 8 | HG02647.hp1 HG02922.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.943+3206dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279279 | |||||
| chrX:7279279
|
G | GAAA | 2 | a0001c0001t0002g0136a0001c0008t0005g0134 | 2 | HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.943+3204_943+3206d others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279279 | |||||
| chrX:7279279
|
GA | G | 9 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.943+3206delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279279 | |||||
| chrX:7279292
|
A | AAAAT | 1 | a0001c0001t0035g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.943+3206_943+3207i others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279292 | |||||
| chrX:7279292
|
A | AAAT | 1 | a0001c0001t0005g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.943+3206_943+3207i others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279292 | |||||
| chrX:7279292
|
A | AAATAT | 4 | a0001c0001t0005g0218a0001c0001t0005g0226a0001c0001t0038g0219others(1): Show | 4 | HG02258.hp1 HG02486.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+3206_943+3207i others(7): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279292 | |||||
| chrX:7279292
|
A | AAATATAT others(2): Show |
1 | a0001c0001t0005g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.943+3206_943+3207i others(11): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279292 | |||||
| chrX:7279292
|
A | AAT | 9 | a0001c0001t0002g0180a0001c0001t0002g0182a0001c0001t0002g0186others(6): Show | 9 | HG00609.hp1 HG00673.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.943+3224_943+3225d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279292 | |||||
| chrX:7279292
|
A | AATAT | 1 | a0001c0001t0002g0194 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.943+3222_943+3225d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279292 | |||||
| chrX:7279292
|
A | AT | 2 | a0001c0001t0002g0104a0002c0002t0020g0009 | 2 | HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.943+3205_943+3206i others(3): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279292 | ||||||
| chrX:7279292
|
A | ATATAT | 3 | a0001c0001t0023g0228a0001c0001t0037g0224a0004c0009t0002g0225 | 3 | HG01074.hp1 HG01106.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.943+3205_943+3206i others(7): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279292 | ||||||
| chrX:7279292
|
A | ATATATAT | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG02109.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.943+3205_943+3206i others(9): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279292 | ||||||
| chrX:7279292
|
A | T | 27 | a0001c0001t0001g0019a0001c0001t0001g0082a0001c0001t0002g0004others(24): Show | 27 | HG00558.hp1 HG00621.hp1 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.943+3205A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279292 | ||||||
| chrX:7279293
|
AT | A | 9 | a0001c0001t0001g0110a0001c0001t0001g0130a0001c0001t0003g0113others(6): Show | 9 | HG01943.hp1 HG02040.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.943+3207delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279293 | ||||||
| chrX:7279294
|
T | A | 63 | a0001c0001t0001g0035a0001c0001t0001g0060a0001c0001t0001g0062others(60): Show | 63 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.943+3207T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279294 | ||||||
| chrX:7279309
|
ATATGTGT others(1): Show |
A | 1 | a0001c0001t0002g0181 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.943+3224_943+3231d others(10): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279309 | |||||
| chrX:7279311
|
A | ATATG | 2 | a0001c0001t0002g0199a0001c0001t0005g0138 | 2 | HG01952.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.943+3225_943+3226i others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279311 | |||||
| chrX:7279311
|
A | ATATGTG | 2 | a0001c0001t0001g0014a0001c0001t0013g0051 | 2 | HG01256.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.943+3225_943+3226i others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279311 | |||||
| chrX:7279311
|
A | ATG | 2 | a0001c0001t0002g0080a0001c0001t0002g0179 | 2 | HG02723.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.943+3250_943+3251d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279311 | |||||
| chrX:7279311
|
A | G | 4 | a0001c0001t0001g0017a0001c0001t0002g0136a0001c0001t0002g0205others(1): Show | 4 | HG02897.hp2 HG03453.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+3224A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279311 | ||||||
| chrX:7279311
|
ATG | A | 1 | a0001c0001t0002g0213 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.943+3250_943+3251d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279311 | |||||
| chrX:7279311
|
ATGTG | A | 1 | a0001c0001t0002g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.943+3248_943+3251d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279311 | |||||
| chrX:7279311
|
ATGTGTGT others(5): Show |
A | 2 | a0001c0001t0003g0113a0001c0001t0003g0129 | 2 | HG01943.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.943+3240_943+3251d others(14): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279311 | |||||
| chrX:7279311
|
ATGTGTGT others(7): Show |
A | 58 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(55): Show | 58 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.943+3238_943+3251d others(16): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279311 | |||||
| chrX:7279313
|
G | A | 13 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0005g0056others(10): Show | 13 | HG01074.hp1 HG01109.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.943+3226G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279313 | ||||||
| chrX:7279315
|
G | A | 1 | a0001c0001t0023g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.943+3228G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279315 | ||||||
| chrX:7279325
|
G | A | 1 | a0001c0001t0003g0113 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.943+3238G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279325 | ||||||
| chrX:7279331
|
GTGTGTGT others(1): Show |
G | 1 | a0001c0001t0005g0056 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.943+3252_943+3259d others(10): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279331 | |||||
| chrX:7279333
|
GTGTGTA | G | 5 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG01109.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+3252_943+3257d others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279333 | |||||
| chrX:7279337
|
G | GTGTA | 6 | a0001c0001t0002g0106a0001c0001t0002g0135a0001c0001t0002g0136others(3): Show | 6 | HG02897.hp2 HG02970.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.943+3251_943+3252i others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279337 | |||||
| chrX:7279337
|
G | GTGTGTA | 2 | a0001c0001t0002g0104a0001c0001t0002g0137 | 2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.943+3251_943+3252i others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279337 | |||||
| chrX:7279339
|
A | ATG | 1 | a0001c0001t0005g0138 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.943+3270_943+3271d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279339 | |||||
| chrX:7279339
|
A | G | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(69): Show | 74 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.943+3252A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279339 | ||||||
| chrX:7279341
|
G | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0061a0001c0001t0001g0068others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+3254G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279341 | ||||||
| chrX:7279341
|
G | GTA | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(53): Show | 58 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.943+3255_943+3256i others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279341 | |||||
| chrX:7279341
|
G | GTGTA | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.943+3257_943+3258i others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279341 | |||||
| chrX:7279357
|
G | A | 7 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0222others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.943+3270G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279357 | ||||||
| chrX:7279359
|
A | ATG | 7 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0222others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.943+3273_943+3274i others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279359 | |||||
| chrX:7279359
|
A | ATGTGTGT others(11): Show |
1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.943+3273_943+3274i others(20): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279359 | |||||
| chrX:7279359
|
A | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(58): Show | 63 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.943+3272A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279359 | ||||||
| chrX:7279361
|
A | ATG | 1 | a0001c0001t0005g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.943+3290_943+3291d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279361 | |||||
| chrX:7279361
|
A | ATGTG | 3 | a0001c0001t0035g0229a0001c0001t0037g0224a0004c0009t0002g0225 | 3 | HG01106.hp1 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.943+3288_943+3291d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279361 | |||||
| chrX:7279361
|
A | G | 7 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0222others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.943+3274A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279361 | ||||||
| chrX:7279361
|
ATG | A | 11 | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0055others(8): Show | 11 | HG01070.hp2 HG01109.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.943+3290_943+3291d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279361 | |||||
| chrX:7279363
|
G | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(59): Show | 64 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.943+3276G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279363 | ||||||
| chrX:7279369
|
GTGTGTGT others(9): Show |
G | 1 | a0001c0001t0002g0200 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.943+3308_943+3323d others(18): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279369 | |||||
| chrX:7279373
|
GTGTGTAT others(5): Show |
G | 1 | a0001c0001t0023g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.943+3292_943+3303d others(14): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279373 | |||||
| chrX:7279379
|
A | G | 1 | a0001c0001t0040g0227 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.943+3292A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279379 | ||||||
| chrX:7279413
|
C | CTG | 2 | a0001c0001t0004g0198a0001c0001t0024g0211 | 2 | NA18959.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.943+3352_943+3353d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279413 | |||||
| chrX:7279413
|
C | CTGTGTG | 1 | a0001c0001t0002g0213 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.943+3348_943+3353d others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279413 | |||||
| chrX:7279413
|
CTG | C | 3 | a0001c0001t0002g0086a0001c0001t0002g0092a0001c0001t0002g0099 | 3 | HG01255.hp1 HG01361.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.943+3352_943+3353d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279413 | |||||
| chrX:7279413
|
CTGTG | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0053a0002c0002t0020g0009others(1): Show | 4 | HG02257.hp2 NA18951.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+3350_943+3353d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279413 | |||||
| chrX:7279413
|
CTGTGTG | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(152): Show | 157 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.943+3348_943+3353d others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7279413 | |||||
| chrX:7279697
|
T | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(224): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.943+3610T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279697 | ||||||
| chrX:7279807
|
C | G | 1 | a0001c0001t0035g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.943+3720C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7279807 | ||||||
| chrX:7280028
|
C | T | 75 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.943+3941C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7280028 | ||||||
| chrX:7280071
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.943+3984A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7280071 | ||||||
| chrX:7280337
|
A | C | 1 | a0001c0001t0003g0152 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.943+4250A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7280337 | ||||||
| chrX:7280428
|
T | C | 75 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.943+4341T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7280428 | ||||||
| chrX:7280580
|
T | C | 75 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0114others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.943+4493T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7280580 | ||||||
| chrX:7280628
|
G | A | 1 | a0005c0005t0003g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.943+4541G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7280628 | ||||||
| chrX:7281163
|
C | CA | 3 | a0001c0001t0001g0014a0001c0001t0002g0135a0001c0001t0025g0202 | 3 | HG03516.hp1 NA19057.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.943+5091dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7281163 | |||||
| chrX:7281163
|
CA | C | 2 | a0001c0001t0021g0096a0002c0002t0027g0097 | 2 | NA19058.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.943+5091delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7281163 | |||||
| chrX:7281349
|
C | T | 1 | a0001c0001t0013g0051 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.943+5262C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7281349 | ||||||
| chrX:7281435
|
A | G | 1 | a0001c0001t0002g0203 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.943+5348A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7281435 | ||||||
| chrX:7281594
|
C | T | 1 | a0001c0001t0015g0102 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.943+5507C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7281594 | ||||||
| chrX:7281600
|
A | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0149 | 2 | HG01243.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.943+5513A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7281600 | ||||||
| chrX:7281619
|
G | A | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.943+5532G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7281619 | ||||||
| chrX:7281789
|
C | T | 1 | a0001c0001t0006g0161 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.943+5702C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7281789 | ||||||
| chrX:7281876
|
A | G | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.943+5789A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7281876 | ||||||
| chrX:7282185
|
GGTTT | G | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.943+6122_943+6125d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7282185 | |||||
| chrX:7282185
|
GGTTTGTT others(1): Show |
G | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.943+6118_943+6125d others(10): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7282185 | |||||
| chrX:7282425
|
T | C | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.943+6338T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7282425 | ||||||
| chrX:7282743
|
A | G | 2 | a0001c0001t0002g0135a0001c0001t0026g0143 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.943+6656A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7282743 | ||||||
| chrX:7282993
|
C | T | 1 | a0001c0001t0002g0192 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.943+6906C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7282993 | ||||||
| chrX:7283755
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.943+7668G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7283755 | ||||||
| chrX:7283863
|
G | C | 2 | a0001c0001t0002g0183a0001c0001t0002g0185 | 2 | NA19066.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.943+7776G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7283863 | ||||||
| chrX:7283910
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(67): Show | 72 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.943+7823G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7283910 | ||||||
| chrX:7284016
|
C | T | 1 | a0001c0001t0006g0161 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.943+7929C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7284016 | ||||||
| chrX:7284173
|
T | C | 1 | a0001c0001t0005g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.943+8086T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7284173 | ||||||
| chrX:7284295
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.943+8208G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7284295 | ||||||
| chrX:7284472
|
G | A | 73 | a0001c0001t0001g0087a0001c0001t0001g0110a0001c0001t0001g0130others(70): Show | 73 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.943+8385G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7284472 | ||||||
| chrX:7284542
|
C | A | 1 | a0001c0001t0003g0124 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.943+8455C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7284542 | ||||||
| chrX:7284639
|
T | C | 1 | a0001c0001t0028g0195 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.943+8552T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7284639 | ||||||
| chrX:7284946
|
CTGA | C | 1 | a0001c0001t0002g0212 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.943+8865_943+8867d others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7284946 | |||||
| chrX:7285045
|
T | C | 1 | a0001c0001t0011g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.943+8958T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7285045 | ||||||
| chrX:7285076
|
GATA | G | 1 | a0001c0001t0001g0010 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.943+8992_943+8994d others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7285076 | |||||
| chrX:7285619
|
G | C | 1 | a0001c0001t0005g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.943+9532G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7285619 | ||||||
| chrX:7285620
|
A | G | 1 | a0001c0001t0011g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.943+9533A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7285620 | ||||||
| chrX:7285688
|
T | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(156): Show | 161 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.943+9601T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7285688 | ||||||
| chrX:7285995
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(67): Show | 72 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.943+9908G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7285995 | ||||||
| chrX:7286145
|
A | ATGTG | 1 | a0006c0007t0001g0039 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.943+10064_943+1006 others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7286145 | |||||
| chrX:7286173
|
A | G | 1 | a0001c0001t0001g0005 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.943+10086A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7286173 | ||||||
| chrX:7286239
|
T | A | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.943+10152T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7286239 | ||||||
| chrX:7286905
|
T | C | 2 | a0001c0001t0003g0169a0001c0001t0009g0170 | 2 | NA18965.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.943+10818T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7286905 | ||||||
| chrX:7287153
|
A | G | 4 | a0001c0001t0002g0197a0001c0001t0007g0126a0001c0001t0008g0177others(1): Show | 4 | HG00323.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+11066A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7287153 | ||||||
| chrX:7287240
|
G | GA | 1 | a0002c0002t0020g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.943+11162dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7287240 | |||||
| chrX:7287658
|
T | A | 9 | a0001c0001t0003g0101a0001c0001t0003g0109a0001c0001t0003g0113others(6): Show | 9 | HG00738.hp1 HG01081.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.943+11571T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7287658 | ||||||
| chrX:7287678
|
T | TTTTA | 75 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.943+11611_943+1161 others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7287678 | |||||
| chrX:7287678
|
T | TTTTATTT others(1): Show |
1 | a0001c0001t0003g0168 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.943+11607_943+1161 others(12): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7287678 | |||||
| chrX:7287710
|
G | A | 88 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(85): Show | 88 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(85): Show |
intron_variant | MODIFIER | c.943+11623G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7287710 | ||||||
| chrX:7287860
|
T | C | 16 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(13): Show | 16 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.943+11773T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7287860 | ||||||
| chrX:7287973
|
C | G | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.943+11886C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7287973 | ||||||
| chrX:7288157
|
C | CT | 93 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0068others(90): Show | 93 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.943+12080dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7288157 | |||||
| chrX:7288157
|
C | CTT | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(64): Show | 69 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.943+12079_943+1208 others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7288157 | |||||
| chrX:7288333
|
C | T | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.943+12246C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7288333 | ||||||
| chrX:7288639
|
C | CGT | 12 | a0001c0001t0002g0099a0001c0001t0002g0181a0001c0001t0002g0183others(9): Show | 12 | HG00323.hp1 HG00558.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.943+12595_943+1259 others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7288639 | |||||
| chrX:7288639
|
C | CGTGT | 4 | a0001c0001t0002g0180a0001c0001t0002g0186a0001c0001t0002g0201others(1): Show | 4 | HG00323.hp2 HG00673.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+12593_943+1259 others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7288639 | |||||
| chrX:7288639
|
C | CGTGTGT | 1 | a0001c0001t0002g0086 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.943+12591_943+1259 others(10): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7288639 | |||||
| chrX:7288639
|
CGT | C | 13 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0058others(10): Show | 13 | HG00099.hp2 HG01109.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.943+12595_943+1259 others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7288639 | |||||
| chrX:7288639
|
CGTGT | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(72): Show | 77 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.943+12593_943+1259 others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7288639 | |||||
| chrX:7288639
|
CGTGTGT | C | 9 | a0001c0001t0001g0114a0001c0001t0001g0149a0001c0001t0002g0104others(6): Show | 9 | HG00280.hp1 HG01243.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.943+12591_943+1259 others(10): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7288639 | |||||
| chrX:7288639
|
CGTGTGTG others(1): Show |
C | 49 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0044others(46): Show | 49 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.943+12589_943+1259 others(12): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7288639 | |||||
| chrX:7288639
|
CGTGTGTG others(3): Show |
C | 4 | a0001c0001t0001g0014a0001c0001t0003g0128a0001c0001t0003g0163others(1): Show | 4 | HG02273.hp1 HG04228.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.943+12587_943+1259 others(14): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7288639 | |||||
| chrX:7288639
|
CGTGTGTG others(5): Show |
C | 1 | a0001c0001t0010g0145 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.943+12585_943+1259 others(16): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7288639 | |||||
| chrX:7288639
|
CGTGTGTG others(23): Show |
C | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.943+12567_943+1259 others(34): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7288639 | |||||
| chrX:7289517
|
C | G | 1 | a0002c0002t0020g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.943+13430C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7289517 | ||||||
| chrX:7289853
|
C | A | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.943+13766C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7289853 | ||||||
| chrX:7290100
|
T | C | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.943+14013T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7290100 | ||||||
| chrX:7290231
|
A | G | 1 | a0001c0001t0003g0152 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.943+14144A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7290231 | ||||||
| chrX:7290351
|
G | C | 1 | a0001c0001t0001g0014 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.943+14264G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7290351 | ||||||
| chrX:7290360
|
ATAATAT | A | 3 | a0001c0001t0001g0069a0001c0001t0012g0028a0001c0001t0012g0029 | 3 | HG01069.hp1 HG01071.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.943+14279_943+1428 others(10): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7290360 | |||||
| chrX:7290373
|
T | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0011g0026 | 3 | HG00621.hp1 NA18975.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.943+14286T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7290373 | ||||||
| chrX:7290393
|
G | A | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.943+14306G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7290393 | ||||||
| chrX:7290519
|
A | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0149 | 2 | HG01243.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.943+14432A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7290519 | ||||||
| chrX:7290957
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.944-14089C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7290957 | ||||||
| chrX:7291142
|
G | A | 1 | a0001c0001t0037g0224 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.944-13904G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7291142 | ||||||
| chrX:7291194
|
G | T | 2 | a0001c0001t0002g0183a0001c0001t0002g0185 | 2 | NA19066.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.944-13852G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7291194 | ||||||
| chrX:7291317
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.944-13729G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7291317 | ||||||
| chrX:7291386
|
T | A | 74 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(71): Show | 74 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.944-13660T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7291386 | ||||||
| chrX:7291437
|
A | C | 1 | a0001c0001t0002g0203 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.944-13609A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7291437 | ||||||
| chrX:7291489
|
G | C | 1 | a0003c0003t0003g0146 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.944-13557G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7291489 | ||||||
| chrX:7291786
|
A | AT | 3 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0001t0003g0118 | 3 | HG01070.hp1 HG01071.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.944-13250dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7291786 | |||||
| chrX:7291786
|
AT | A | 1 | a0001c0001t0026g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.944-13250delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7291786 | |||||
| chrX:7292515
|
C | T | 1 | a0001c0001t0005g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.944-12531C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7292515 | ||||||
| chrX:7293616
|
TA | T | 1 | a0001c0001t0001g0032 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.944-11427delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7293616 | |||||
| chrX:7293692
|
G | C | 1 | a0001c0001t0001g0054 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.944-11354G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7293692 | ||||||
| chrX:7293897
|
A | AATGAGCT | 1 | a0001c0001t0040g0227 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.944-11144_944-1113 others(11): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7293897 | |||||
| chrX:7293968
|
A | T | 48 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(45): Show | 48 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.944-11078A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7293968 | ||||||
| chrX:7294168
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.944-10878G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7294168 | ||||||
| chrX:7294236
|
G | A | 90 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(87): Show | 90 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.944-10810G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7294236 | ||||||
| chrX:7294609
|
A | G | 3 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0001t0003g0118 | 3 | HG01070.hp1 HG01071.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.944-10437A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7294609 | ||||||
| chrX:7295268
|
CA | C | 1 | a0001c0001t0001g0032 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.944-9771delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7295268 | |||||
| chrX:7295897
|
G | A | 3 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0001t0002g0190 | 3 | HG01934.hp1 NA18981.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.944-9149G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7295897 | ||||||
| chrX:7295998
|
G | A | 2 | a0002c0002t0020g0009a0002c0002t0027g0097 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.944-9048G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7295998 | ||||||
| chrX:7296007
|
G | A | 76 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(73): Show | 76 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.944-9039G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7296007 | ||||||
| chrX:7296166
|
A | G | 2 | a0002c0002t0020g0009a0002c0002t0027g0097 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.944-8880A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7296166 | ||||||
| chrX:7296436
|
A | G | 1 | a0001c0001t0037g0224 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.944-8610A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7296436 | ||||||
| chrX:7296662
|
T | C | 1 | a0004c0009t0002g0225 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.944-8384T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7296662 | ||||||
| chrX:7296764
|
T | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(158): Show | 163 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.944-8282T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7296764 | ||||||
| chrX:7296992
|
G | A | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.944-8054G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7296992 | ||||||
| chrX:7297025
|
A | C | 1 | a0001c0001t0007g0126 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.944-8021A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7297025 | ||||||
| chrX:7297234
|
G | T | 1 | a0001c0001t0002g0213 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.944-7812G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7297234 | ||||||
| chrX:7297257
|
C | CT | 2 | a0001c0001t0001g0020a0001c0001t0002g0099 | 2 | HG02622.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.944-7773dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7297257 | |||||
| chrX:7297257
|
C | CTT | 1 | a0001c0001t0024g0211 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.944-7774_944-7773d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7297257 | |||||
| chrX:7297257
|
CT | C | 7 | a0001c0001t0001g0005a0001c0001t0002g0189a0001c0001t0002g0214others(4): Show | 7 | HG01516.hp1 HG02735.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.944-7773delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7297257 | |||||
| chrX:7297295
|
C | T | 5 | a0001c0001t0006g0158a0001c0001t0006g0160a0001c0001t0006g0161others(2): Show | 5 | HG00639.hp2 HG02004.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-7751C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7297295 | ||||||
| chrX:7297393
|
C | T | 5 | a0001c0001t0006g0158a0001c0001t0006g0160a0001c0001t0006g0161others(2): Show | 5 | HG00639.hp2 HG02004.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-7653C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7297393 | ||||||
| chrX:7297762
|
A | G | 76 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(73): Show | 76 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.944-7284A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7297762 | ||||||
| chrX:7297992
|
G | A | 3 | a0001c0001t0005g0221a0001c0001t0037g0224a0004c0009t0002g0225 | 3 | HG01106.hp1 HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.944-7054G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7297992 | ||||||
| chrX:7298102
|
GA | G | 1 | a0001c0001t0002g0189 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.944-6936delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7298102 | |||||
| chrX:7298150
|
A | G | 2 | a0001c0001t0002g0180a0001c0001t0002g0186 | 2 | HG00673.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.944-6896A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7298150 | ||||||
| chrX:7298300
|
G | T | 74 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(71): Show | 74 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.944-6746G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7298300 | ||||||
| chrX:7298675
|
T | C | 1 | a0001c0001t0002g0197 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.944-6371T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7298675 | ||||||
| chrX:7298710
|
G | A | 5 | a0001c0001t0006g0158a0001c0001t0006g0160a0001c0001t0006g0161others(2): Show | 5 | HG00639.hp2 HG02004.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-6336G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7298710 | ||||||
| chrX:7298830
|
A | G | 2 | a0003c0003t0003g0146a0003c0003t0003g0147 | 2 | NA18957.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.944-6216A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7298830 | ||||||
| chrX:7298962
|
C | CTATGTTT | 1 | a0001c0001t0005g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.944-6080_944-6074d others(9): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7298962 | |||||
| chrX:7298999
|
A | ATTATATA others(26): Show |
1 | a0001c0001t0001g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.944-6030_944-6029i others(35): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7298999 | |||||
| chrX:7299006
|
ATTTATAT others(14): Show |
A | 1 | a0001c0001t0030g0038 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.944-6034_944-6014d others(23): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7299006 | |||||
| chrX:7299017
|
T | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.944-6029T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7299017 | ||||||
| chrX:7299026
|
AT | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(70): Show | 75 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.944-6016delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7299026 | |||||
| chrX:7299027
|
TTTTATTT others(25): Show |
T | 74 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(71): Show | 74 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.944-6005_944-5974d others(34): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7299027 | |||||
| chrX:7299065
|
T | A | 2 | a0001c0001t0002g0182a0001c0001t0002g0206 | 2 | HG00609.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.944-5981T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7299065 | ||||||
| chrX:7299085
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.944-5961A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7299085 | ||||||
| chrX:7299157
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0036g0006 | 2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.944-5889T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7299157 | ||||||
| chrX:7299204
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.944-5842A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7299204 | ||||||
| chrX:7299231
|
TA | T | 4 | a0001c0001t0001g0114a0001c0001t0001g0149a0001c0001t0002g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.944-5814delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7299231 | ||||||
| chrX:7299340
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0070 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.944-5706A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7299340 | ||||||
| chrX:7299399
|
C | T | 1 | a0001c0001t0002g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.944-5647C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7299399 | ||||||
| chrX:7299806
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.944-5240C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7299806 | ||||||
| chrX:7299928
|
A | G | 76 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(73): Show | 76 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.944-5118A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7299928 | ||||||
| chrX:7300311
|
G | C | 4 | a0001c0001t0003g0166a0001c0001t0003g0167a0001c0001t0003g0168others(1): Show | 4 | HG01168.hp2 HG01358.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.944-4735G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7300311 | ||||||
| chrX:7300538
|
G | A | 1 | a0001c0001t0005g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.944-4508G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7300538 | ||||||
| chrX:7300849
|
CA | C | 1 | a0001c0001t0037g0224 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.944-4196delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7300849 | ||||||
| chrX:7300859
|
C | T | 86 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(83): Show | 86 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.944-4187C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7300859 | ||||||
| chrX:7301107
|
T | C | 1 | a0001c0001t0007g0154 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.944-3939T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7301107 | ||||||
| chrX:7301233
|
C | CA | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(183): Show | 188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.944-3803dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7301233 | |||||
| chrX:7301501
|
T | G | 1 | a0001c0001t0025g0202 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.944-3545T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7301501 | ||||||
| chrX:7302187
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.944-2859A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7302187 | ||||||
| chrX:7302868
|
C | T | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.944-2178C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7302868 | ||||||
| chrX:7303398
|
C | T | 5 | a0001c0001t0006g0158a0001c0001t0006g0160a0001c0001t0006g0161others(2): Show | 5 | HG00639.hp2 HG02004.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.944-1648C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7303398 | ||||||
| chrX:7303746
|
T | C | 1 | a0001c0001t0023g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.944-1300T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7303746 | ||||||
| chrX:7304024
|
G | A | 2 | a0001c0001t0002g0086a0001c0001t0002g0092 | 2 | HG01255.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.944-1022G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7304024 | ||||||
| chrX:7304082
|
C | CTG | 52 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(49): Show | 52 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.944-963_944-962dup others(2): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7304082 | |||||
| chrX:7304178
|
T | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(158): Show | 163 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.944-868T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7304178 | ||||||
| chrX:7304321
|
T | C | 1 | a0004c0009t0002g0225 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.944-725T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7304321 | ||||||
| chrX:7304401
|
TGTTA | T | 1 | a0001c0001t0002g0139 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.944-641_944-638del others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 7304401 | |||||
| chrX:7304457
|
C | T | 3 | a0001c0001t0002g0144a0001c0001t0010g0100a0001c0001t0010g0145 | 3 | HG02055.hp1 HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.944-589C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7304457 | ||||||
| chrX:7304901
|
A | T | 1 | a0001c0001t0005g0138 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.944-145A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 7/10 | chrX | 7304901 | ||||||
| chrX:7305334
|
A | G | 1 | a0001c0001t0026g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1081+151A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7305334 | ||||||
| chrX:7305408
|
T | A | 1 | a0001c0001t0003g0123 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1081+225T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7305408 | ||||||
| chrX:7305428
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064 | 3 | HG02922.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1081+245C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7305428 | ||||||
| chrX:7305483
|
C | G | 1 | a0001c0001t0001g0044 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1081+300C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7305483 | ||||||
| chrX:7306015
|
A | G | 1 | a0001c0001t0002g0200 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1081+832A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7306015 | ||||||
| chrX:7306253
|
A | G | 2 | a0001c0001t0002g0180a0001c0001t0002g0186 | 2 | HG00673.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1081+1070A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7306253 | ||||||
| chrX:7306401
|
G | A | 2 | a0001c0001t0003g0112a0001c0001t0003g0148 | 2 | NA18951.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1081+1218G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7306401 | ||||||
| chrX:7306934
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(46): Show | 51 | HG00558.hp2 HG00621.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1081+1751C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7306934 | ||||||
| chrX:7306967
|
G | A | 13 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(10): Show | 13 | HG02055.hp1 HG02559.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1081+1784G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7306967 | ||||||
| chrX:7307180
|
A | G | 77 | a0001c0001t0001g0030a0001c0001t0001g0082a0001c0001t0001g0087others(74): Show | 77 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.1081+1997A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7307180 | ||||||
| chrX:7307567
|
G | T | 1 | a0001c0001t0001g0059 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1081+2384G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7307567 | ||||||
| chrX:7307715
|
A | G | 1 | a0001c0001t0002g0192 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1081+2532A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7307715 | ||||||
| chrX:7307718
|
A | G | 2 | a0001c0001t0002g0183a0001c0001t0002g0185 | 2 | NA19066.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1081+2535A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7307718 | ||||||
| chrX:7307968
|
A | G | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1081+2785A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7307968 | ||||||
| chrX:7308231
|
C | T | 1 | a0001c0001t0005g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1081+3048C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7308231 | ||||||
| chrX:7308431
|
G | A | 1 | a0001c0001t0037g0224 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1081+3248G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7308431 | ||||||
| chrX:7308503
|
C | T | 3 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0210 | 3 | HG03491.hp1 HG03492.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1081+3320C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7308503 | ||||||
| chrX:7308593
|
G | C | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1081+3410G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7308593 | ||||||
| chrX:7308611
|
CT | C | 1 | a0001c0001t0003g0175 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1081+3438delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7308611 | |||||
| chrX:7308924
|
T | G | 1 | a0001c0001t0001g0012 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1081+3741T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7308924 | ||||||
| chrX:7308946
|
C | T | 5 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG01109.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1081+3763C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7308946 | ||||||
| chrX:7309013
|
C | CT | 2 | a0003c0003t0003g0146a0003c0003t0003g0147 | 2 | NA18957.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1081+3840dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7309013 | |||||
| chrX:7309415
|
A | G | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1081+4232A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7309415 | ||||||
| chrX:7309567
|
T | TA | 1 | a0001c0001t0003g0166 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1081+4387dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7309567 | |||||
| chrX:7309575
|
A | G | 1 | a0001c0001t0007g0126 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1081+4392A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7309575 | ||||||
| chrX:7309598
|
T | TA | 87 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(84): Show | 87 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(84): Show |
intron_variant | MODIFIER | c.1081+4425dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7309598 | |||||
| chrX:7309598
|
T | TAA | 2 | a0002c0002t0020g0009a0002c0002t0027g0097 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1081+4424_1081+442 others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7309598 | |||||
| chrX:7309603
|
A | AG | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(69): Show | 74 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1081+4420_1081+442 others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7309603 | ||||||
| chrX:7309909
|
A | G | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1081+4726A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7309909 | ||||||
| chrX:7309909
|
A | T | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+4726A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7309909 | ||||||
| chrX:7309912
|
TAATTC | T | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+4730_1081+473 others(9): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7309912 | ||||||
| chrX:7309922
|
CA | C | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+4742delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7309922 | |||||
| chrX:7309931
|
GA | G | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+4751delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7309931 | |||||
| chrX:7310144
|
A | AC | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+4963dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7310144 | |||||
| chrX:7310223
|
G | GT | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+5040_1081+504 others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7310223 | ||||||
| chrX:7310387
|
AT | A | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+5207delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7310387 | |||||
| chrX:7310426
|
TG | T | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+5245delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7310426 | |||||
| chrX:7310457
|
A | G | 1 | a0001c0001t0004g0078 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1081+5274A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7310457 | ||||||
| chrX:7310495
|
G | GA | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+5314dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7310495 | |||||
| chrX:7310581
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1081+5398T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7310581 | ||||||
| chrX:7310706
|
A | AC | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+5525dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7310706 | |||||
| chrX:7310898
|
C | CA | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+5716dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7310898 | |||||
| chrX:7310991
|
A | AC | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+5812dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7310991 | |||||
| chrX:7311056
|
CT | C | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+5876delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7311056 | |||||
| chrX:7311130
|
T | TC | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+5948dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7311130 | |||||
| chrX:7311256
|
A | AG | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+6074dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7311256 | |||||
| chrX:7311586
|
AC | A | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+6405delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7311586 | |||||
| chrX:7311771
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1081+6588G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7311771 | ||||||
| chrX:7311777
|
G | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0130 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1081+6594G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7311777 | ||||||
| chrX:7311853
|
C | CA | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+6677dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7311853 | |||||
| chrX:7311875
|
A | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0130 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1081+6692A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7311875 | ||||||
| chrX:7311892
|
T | G | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+6709T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7311892 | ||||||
| chrX:7311944
|
T | C | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1081+6761T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7311944 | ||||||
| chrX:7311959
|
C | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0149a0001c0001t0002g0099 | 3 | HG01243.hp1 HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1081+6776C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7311959 | ||||||
| chrX:7312119
|
G | GT | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+6940dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7312119 | |||||
| chrX:7312133
|
T | TC | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+6951dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7312133 | |||||
| chrX:7312142
|
C | CT | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+6963dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7312142 | |||||
| chrX:7312326
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0032 | 2 | NA18961.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1081+7143G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7312326 | ||||||
| chrX:7312485
|
GT | G | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+7305delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7312485 | |||||
| chrX:7313007
|
T | C | 1 | a0001c0001t0002g0036 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1081+7824T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7313007 | ||||||
| chrX:7313114
|
AC | A | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+7932delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7313114 | ||||||
| chrX:7313196
|
A | AT | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1081+8017dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7313196 | |||||
| chrX:7313767
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1081+8584C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7313767 | ||||||
| chrX:7313963
|
C | T | 1 | a0001c0001t0002g0213 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1081+8780C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7313963 | ||||||
| chrX:7314029
|
T | C | 5 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG01192.hp1 HG01361.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1081+8846T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7314029 | ||||||
| chrX:7314395
|
A | G | 2 | a0003c0003t0003g0146a0003c0003t0003g0147 | 2 | NA18957.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1081+9212A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7314395 | ||||||
| chrX:7314475
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1081+9292G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7314475 | ||||||
| chrX:7314775
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1081+9592A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7314775 | ||||||
| chrX:7314818
|
A | G | 5 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0011g0041others(2): Show | 5 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1081+9635A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7314818 | ||||||
| chrX:7315056
|
A | G | 1 | a0001c0001t0023g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1081+9873A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7315056 | ||||||
| chrX:7315367
|
G | A | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1082-9972G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7315367 | ||||||
| chrX:7316012
|
C | T | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1082-9327C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7316012 | ||||||
| chrX:7316013
|
A | G | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1082-9326A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7316013 | ||||||
| chrX:7316238
|
TC | T | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1082-9095delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7316238 | |||||
| chrX:7316245
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0053 | 2 | NA18951.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1082-9094G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7316245 | ||||||
| chrX:7316303
|
C | CA | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1082-9030dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7316303 | |||||
| chrX:7316337
|
T | TG | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1082-9000dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7316337 | |||||
| chrX:7316658
|
A | AC | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1082-8680dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7316658 | |||||
| chrX:7316965
|
C | CT | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1082-8373dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7316965 | |||||
| chrX:7317026
|
C | A | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1082-8313C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7317026 | ||||||
| chrX:7317190
|
GA | G | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1082-8147delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7317190 | |||||
| chrX:7317209
|
C | CA | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1082-8125dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7317209 | |||||
| chrX:7317285
|
G | GT | 69 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(66): Show | 69 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.1082-8043dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7317285 | |||||
| chrX:7317454
|
G | GGTTT | 4 | a0001c0001t0001g0114a0001c0001t0001g0149a0001c0001t0002g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1082-7856_1082-785 others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7317454 | |||||
| chrX:7317454
|
GGTTT | G | 3 | a0001c0001t0001g0060a0001c0001t0006g0161a0001c0001t0013g0033 | 3 | NA19063.hp1 NA20300.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1082-7856_1082-785 others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7317454 | |||||
| chrX:7317529
|
C | CT | 1 | a0001c0001t0019g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1082-7810_1082-780 others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7317529 | ||||||
| chrX:7317530
|
G | A | 1 | a0001c0001t0019g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1082-7809G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7317530 | ||||||
| chrX:7317531
|
T | G | 1 | a0001c0001t0019g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1082-7808T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7317531 | ||||||
| chrX:7317533
|
A | G | 1 | a0001c0001t0019g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1082-7806A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7317533 | ||||||
| chrX:7317548
|
G | A | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1082-7791G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7317548 | ||||||
| chrX:7317631
|
G | A | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1082-7708G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7317631 | ||||||
| chrX:7317815
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1082-7524G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7317815 | ||||||
| chrX:7317922
|
G | A | 5 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG01109.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1082-7417G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7317922 | ||||||
| chrX:7318545
|
T | C | 1 | a0002c0002t0020g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1082-6794T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7318545 | ||||||
| chrX:7318717
|
A | G | 1 | a0001c0001t0002g0194 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1082-6622A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7318717 | ||||||
| chrX:7318929
|
T | A | 53 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0003g0101others(50): Show | 53 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.1082-6410T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7318929 | ||||||
| chrX:7318996
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0130 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1082-6343A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7318996 | ||||||
| chrX:7319069
|
T | A | 3 | a0001c0001t0002g0080a0001c0001t0002g0094a0001c0001t0002g0098 | 3 | HG02723.hp2 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1082-6270T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7319069 | ||||||
| chrX:7319955
|
TTA | T | 1 | a0006c0007t0001g0039 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1082-5374_1082-537 others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7319955 | |||||
| chrX:7319968
|
TTATATAT others(3): Show |
T | 8 | a0001c0001t0002g0104a0001c0001t0002g0135a0001c0001t0002g0136others(5): Show | 8 | HG02647.hp1 HG02886.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1082-5361_1082-535 others(14): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7319968 | |||||
| chrX:7319978
|
G | T | 76 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(73): Show | 76 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(73): Show |
intron_variant | MODIFIER | c.1082-5361G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7319978 | ||||||
| chrX:7319984
|
ATATT | A | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1082-5351_1082-534 others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7319984 | |||||
| chrX:7319986
|
ATT | A | 2 | a0001c0001t0001g0022a0001c0001t0036g0006 | 2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1082-5351_1082-535 others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7319986 | |||||
| chrX:7319988
|
TTA | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064 | 3 | HG02922.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1082-5341_1082-534 others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7319988 | |||||
| chrX:7319996
|
ATATT | A | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1082-5341_1082-533 others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7319996 | |||||
| chrX:7320002
|
T | A | 1 | a0006c0007t0001g0039 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1082-5337T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7320002 | ||||||
| chrX:7320002
|
T | TTA | 1 | a0001c0001t0002g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1082-5327_1082-532 others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7320002 | |||||
| chrX:7320002
|
T | TTATATAT others(29): Show |
2 | a0001c0001t0001g0025a0001c0001t0030g0038 | 2 | NA19077.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1082-5331_1082-529 others(40): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7320002 | |||||
| chrX:7320004
|
A | T | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1082-5335A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7320004 | ||||||
| chrX:7320004
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0002g0201 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1082-5315_1082-530 others(14): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7320004 | |||||
| chrX:7320014
|
TTATATAT others(5): Show |
T | 2 | a0001c0001t0003g0151a0001c0001t0003g0163 | 2 | NA18999.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1082-5307_1082-529 others(16): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7320014 | |||||
| chrX:7320055
|
ATATATAT others(4): Show |
A | 4 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0072others(1): Show | 4 | HG00741.hp2 HG03654.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1082-5264_1082-525 others(15): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7320055 | |||||
| chrX:7320059
|
A | ATATTTAT others(32): Show |
2 | a0002c0002t0020g0009a0002c0002t0027g0097 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1082-5277_1082-527 others(43): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7320059 | |||||
| chrX:7320079
|
A | G | 68 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(65): Show | 68 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.1082-5260A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7320079 | ||||||
| chrX:7320095
|
AT | A | 2 | a0002c0002t0020g0009a0002c0002t0027g0097 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1082-5238delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7320095 | |||||
| chrX:7320130
|
T | C | 68 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(65): Show | 68 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.1082-5209T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7320130 | ||||||
| chrX:7320131
|
AT | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0149a0001c0001t0002g0099 | 3 | HG01243.hp1 HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1082-5203delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7320131 | |||||
| chrX:7320275
|
A | G | 1 | a0001c0001t0002g0213 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1082-5064A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7320275 | ||||||
| chrX:7320533
|
G | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(224): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1082-4806G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7320533 | ||||||
| chrX:7320711
|
C | T | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1082-4628C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7320711 | ||||||
| chrX:7320798
|
A | T | 1 | a0001c0001t0002g0190 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1082-4541A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7320798 | ||||||
| chrX:7320939
|
A | G | 1 | a0001c0001t0002g0036 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1082-4400A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7320939 | ||||||
| chrX:7321045
|
A | G | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1082-4294A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7321045 | ||||||
| chrX:7321147
|
C | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0149a0001c0001t0002g0099 | 3 | HG01243.hp1 HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1082-4192C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7321147 | ||||||
| chrX:7321170
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1082-4169G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7321170 | ||||||
| chrX:7321228
|
A | C | 14 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(11): Show | 14 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1082-4111A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7321228 | ||||||
| chrX:7321307
|
A | G | 29 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0003g0101others(26): Show | 29 | HG00738.hp1 HG01081.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.1082-4032A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7321307 | ||||||
| chrX:7321322
|
G | A | 59 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0003g0101others(56): Show | 59 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.1082-4017G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7321322 | ||||||
| chrX:7321495
|
A | G | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1082-3844A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7321495 | ||||||
| chrX:7321735
|
A | C | 1 | a0001c0001t0002g0179 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1082-3604A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7321735 | ||||||
| chrX:7321736
|
A | G | 2 | a0001c0001t0004g0078a0001c0001t0004g0090 | 2 | NA18945.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1082-3603A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7321736 | ||||||
| chrX:7322317
|
G | A | 2 | a0003c0003t0003g0146a0003c0003t0003g0147 | 2 | NA18957.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1082-3022G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7322317 | ||||||
| chrX:7322390
|
T | TTC | 1 | a0001c0001t0002g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1082-2933_1082-293 others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7322390 | |||||
| chrX:7322461
|
T | C | 1 | a0001c0001t0028g0195 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1082-2878T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7322461 | ||||||
| chrX:7322481
|
A | C | 2 | a0001c0001t0002g0187a0001c0001t0002g0214 | 2 | HG00099.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1082-2858A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7322481 | ||||||
| chrX:7322549
|
C | T | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1082-2790C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7322549 | ||||||
| chrX:7322550
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG01192.hp1 HG01361.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1082-2789G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7322550 | ||||||
| chrX:7322559
|
C | G | 1 | a0001c0001t0001g0012 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1082-2780C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7322559 | ||||||
| chrX:7322758
|
C | T | 12 | a0001c0001t0005g0218a0001c0001t0005g0220a0001c0001t0005g0221others(9): Show | 12 | HG01074.hp1 HG01106.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1082-2581C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7322758 | ||||||
| chrX:7322885
|
C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0020others(3): Show | 6 | HG00621.hp1 NA18964.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1082-2454C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7322885 | ||||||
| chrX:7323016
|
C | G | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1082-2323C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7323016 | ||||||
| chrX:7323021
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0149a0001c0001t0002g0099 | 3 | HG01243.hp1 HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1082-2318A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7323021 | ||||||
| chrX:7323041
|
C | G | 61 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0110others(58): Show | 61 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.1082-2298C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7323041 | ||||||
| chrX:7323096
|
C | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0149a0001c0001t0002g0099 | 3 | HG01243.hp1 HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1082-2243C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7323096 | ||||||
| chrX:7323214
|
C | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0040 | 2 | NA18964.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1082-2125C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7323214 | ||||||
| chrX:7323225
|
G | GT | 1 | a0001c0001t0040g0227 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1082-2102dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7323225 | |||||
| chrX:7323225
|
GT | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0035others(4): Show | 7 | HG02015.hp1 NA18982.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.1082-2102delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7323225 | |||||
| chrX:7323259
|
C | T | 1 | a0001c0001t0007g0153 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1082-2080C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7323259 | ||||||
| chrX:7323379
|
C | G | 1 | a0001c0001t0023g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1082-1960C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7323379 | ||||||
| chrX:7323709
|
T | A | 1 | a0001c0001t0005g0226 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1082-1630T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7323709 | ||||||
| chrX:7323763
|
G | A | 1 | a0001c0001t0003g0174 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1082-1576G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7323763 | ||||||
| chrX:7323828
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1082-1511A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7323828 | ||||||
| chrX:7323903
|
C | G | 3 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0001t0003g0118 | 3 | HG01070.hp1 HG01071.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1082-1436C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7323903 | ||||||
| chrX:7323957
|
C | G | 1 | a0001c0001t0003g0124 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1082-1382C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7323957 | ||||||
| chrX:7324028
|
C | G | 2 | a0003c0003t0003g0146a0003c0003t0003g0147 | 2 | NA18957.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1082-1311C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7324028 | ||||||
| chrX:7324030
|
C | T | 1 | a0001c0001t0037g0224 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1082-1309C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7324030 | ||||||
| chrX:7324061
|
T | C | 4 | a0001c0001t0001g0114a0001c0001t0001g0149a0001c0001t0002g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1082-1278T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7324061 | ||||||
| chrX:7324131
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1082-1208T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7324131 | ||||||
| chrX:7324171
|
G | C | 2 | a0001c0001t0004g0091a0001c0001t0025g0202 | 2 | NA18980.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1082-1168G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7324171 | ||||||
| chrX:7324185
|
G | C | 6 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1082-1154G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7324185 | ||||||
| chrX:7324198
|
A | G | 74 | a0001c0001t0001g0020a0001c0001t0001g0071a0001c0001t0001g0082others(71): Show | 74 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1082-1141A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7324198 | ||||||
| chrX:7324249
|
A | G | 3 | a0001c0001t0001g0061a0001c0001t0001g0072a0001c0001t0001g0073 | 3 | HG00741.hp2 HG03710.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1082-1090A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7324249 | ||||||
| chrX:7324358
|
C | T | 98 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0110others(95): Show | 98 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.1082-981C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7324358 | ||||||
| chrX:7324426
|
G | A | 1 | a0001c0001t0011g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1082-913G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7324426 | ||||||
| chrX:7324485
|
G | A | 1 | a0001c0001t0005g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1082-854G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7324485 | ||||||
| chrX:7324488
|
A | C | 1 | a0007c0004t0003g0150 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1082-851A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7324488 | ||||||
| chrX:7324592
|
TACAA | T | 1 | a0001c0001t0003g0173 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1082-743_1082-740d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 7324592 | |||||
| chrX:7324673
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1082-666G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7324673 | ||||||
| chrX:7324686
|
G | C | 1 | a0001c0001t0007g0154 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1082-653G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7324686 | ||||||
| chrX:7324809
|
G | C | 12 | a0001c0001t0002g0099a0001c0001t0002g0104a0001c0001t0002g0105others(9): Show | 12 | HG02055.hp1 HG02559.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1082-530G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7324809 | ||||||
| chrX:7324881
|
G | C | 1 | a0001c0001t0001g0027 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1082-458G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7324881 | ||||||
| chrX:7324931
|
C | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0040g0227 | 3 | HG02895.hp1 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1082-408C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7324931 | ||||||
| chrX:7324995
|
A | C | 1 | a0001c0001t0030g0038 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1082-344A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7324995 | ||||||
| chrX:7325007
|
G | C | 64 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(61): Show | 64 | HG00099.hp1 HG00558.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1082-332G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7325007 | ||||||
| chrX:7325235
|
G | A | 1 | a0001c0001t0003g0175 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1082-104G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7325235 | ||||||
| chrX:7325251
|
T | C | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1082-88T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7325251 | ||||||
| chrX:7325263
|
G | A | 69 | a0001c0001t0001g0035a0001c0001t0001g0082a0001c0001t0001g0087others(66): Show | 69 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.1082-76G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7325263 | ||||||
| chrX:7325284
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1082-55C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7325284 | ||||||
| chrX:7325286
|
T | A | 1 | a0001c0001t0026g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1082-53T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 8/10 | chrX | 7325286 | ||||||
| chrX:7325513
|
G | C | 2 | a0001c0001t0003g0107a0001c0001t0003g0108 | 2 | HG02083.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1241+15G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7325513 | ||||||
| chrX:7325535
|
C | G | 1 | a0001c0001t0019g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1241+37C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7325535 | ||||||
| chrX:7325608
|
G | GT | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1241+114dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7325608 | |||||
| chrX:7326164
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(186): Show | 191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1241+666A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7326164 | ||||||
| chrX:7326398
|
G | C | 1 | a0001c0001t0004g0076 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1241+900G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7326398 | ||||||
| chrX:7326559
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1241+1061G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7326559 | ||||||
| chrX:7326667
|
T | A | 2 | a0002c0002t0020g0009a0002c0002t0027g0097 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1241+1169T>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7326667 | ||||||
| chrX:7327014
|
C | G | 2 | a0003c0003t0003g0146a0003c0003t0003g0147 | 2 | NA18957.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1241+1516C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7327014 | ||||||
| chrX:7327376
|
C | CT | 10 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(7): Show | 10 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1241+1889dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7327376 | |||||
| chrX:7327376
|
CT | C | 1 | a0001c0001t0002g0196 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1241+1889delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7327376 | |||||
| chrX:7327388
|
C | CT | 1 | a0001c0001t0026g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1241+1902dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7327388 | |||||
| chrX:7327388
|
CT | C | 1 | a0001c0001t0041g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1241+1902delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7327388 | |||||
| chrX:7327447
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(130): Show | 135 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.1241+1949G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7327447 | ||||||
| chrX:7327470
|
G | A | 1 | a0001c0001t0003g0166 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1241+1972G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7327470 | ||||||
| chrX:7327654
|
G | A | 3 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0001t0003g0118 | 3 | HG01070.hp1 HG01071.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1241+2156G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7327654 | ||||||
| chrX:7328194
|
C | T | 1 | a0001c0001t0025g0202 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1241+2696C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7328194 | ||||||
| chrX:7328275
|
TG | T | 1 | a0001c0001t0007g0154 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1241+2782delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7328275 | |||||
| chrX:7328555
|
A | AT | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(147): Show | 152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1241+3074dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7328555 | |||||
| chrX:7328555
|
A | ATT | 20 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0030others(17): Show | 20 | HG01515.hp1 HG02040.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.1241+3073_1241+307 others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7328555 | |||||
| chrX:7328555
|
AT | A | 12 | a0001c0001t0005g0056a0001c0001t0005g0138a0001c0001t0005g0218others(9): Show | 12 | HG01106.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1241+3074delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7328555 | |||||
| chrX:7328705
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1241+3207G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7328705 | ||||||
| chrX:7329895
|
A | ATTGTTG | 1 | a0001c0001t0013g0051 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1242-4073_1242-406 others(10): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7329895 | |||||
| chrX:7329895
|
ATTG | A | 1 | a0001c0001t0001g0014 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1242-4070_1242-406 others(7): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7329895 | |||||
| chrX:7330095
|
C | G | 13 | a0001c0001t0005g0056a0001c0001t0005g0138a0001c0001t0005g0218others(10): Show | 13 | HG01106.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1242-3891C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7330095 | ||||||
| chrX:7330278
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1242-3708A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7330278 | ||||||
| chrX:7330331
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1242-3655G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7330331 | ||||||
| chrX:7330381
|
C | T | 1 | a0001c0001t0002g0205 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1242-3605C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7330381 | ||||||
| chrX:7330914
|
C | T | 1 | a0001c0001t0007g0126 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1242-3072C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7330914 | ||||||
| chrX:7331115
|
C | T | 13 | a0001c0001t0005g0056a0001c0001t0005g0138a0001c0001t0005g0218others(10): Show | 13 | HG01106.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1242-2871C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7331115 | ||||||
| chrX:7331125
|
A | G | 2 | a0001c0001t0038g0219a0001c0001t0040g0227 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1242-2861A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7331125 | ||||||
| chrX:7331461
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1242-2525C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7331461 | ||||||
| chrX:7331700
|
C | A | 1 | a0001c0001t0005g0138 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1242-2286C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7331700 | ||||||
| chrX:7331887
|
T | TA | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(128): Show | 133 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.1242-2079dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7331887 | |||||
| chrX:7331887
|
T | TAA | 14 | a0001c0001t0001g0037a0001c0001t0002g0099a0001c0001t0002g0104others(11): Show | 14 | HG02055.hp1 HG02559.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.1242-2080_1242-207 others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7331887 | |||||
| chrX:7331887
|
T | TAAA | 1 | a0001c0001t0002g0106 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1242-2081_1242-207 others(7): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7331887 | |||||
| chrX:7331887
|
TA | T | 4 | a0001c0001t0002g0203a0001c0001t0002g0210a0001c0001t0007g0154others(1): Show | 4 | HG00323.hp2 HG01070.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1242-2079delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7331887 | |||||
| chrX:7332071
|
A | G | 1 | a0001c0008t0005g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1242-1915A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7332071 | ||||||
| chrX:7332163
|
C | CA | 2 | a0001c0001t0003g0157a0006c0007t0001g0039 | 2 | HG04184.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1242-1811dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7332163 | |||||
| chrX:7332286
|
G | A | 1 | a0001c0001t0005g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1242-1700G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7332286 | ||||||
| chrX:7332331
|
T | TA | 5 | a0001c0001t0002g0135a0001c0001t0002g0184a0001c0001t0003g0133others(2): Show | 5 | HG01123.hp1 HG01168.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.1242-1640dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7332331 | |||||
| chrX:7332331
|
TA | T | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1242-1640delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7332331 | |||||
| chrX:7332432
|
G | GA | 3 | a0001c0001t0002g0135a0001c0001t0002g0217a0001c0001t0005g0220 | 3 | HG01175.hp1 HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1242-1540dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7332432 | |||||
| chrX:7332432
|
GA | G | 1 | a0001c0001t0001g0049 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1242-1540delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7332432 | |||||
| chrX:7332569
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1242-1417G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7332569 | ||||||
| chrX:7332745
|
G | A | 1 | a0001c0001t0035g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1242-1241G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7332745 | ||||||
| chrX:7332821
|
C | T | 1 | a0001c0001t0002g0201 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1242-1165C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7332821 | ||||||
| chrX:7332893
|
T | TAGAATAT others(313): Show |
1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1242-1082_1242-108 others(324): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 7332893 | |||||
| chrX:7332943
|
G | A | 1 | a0001c0001t0017g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1242-1043G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7332943 | ||||||
| chrX:7332981
|
T | C | 2 | a0001c0001t0004g0084a0001c0001t0004g0085 | 2 | NA19005.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1242-1005T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7332981 | ||||||
| chrX:7333055
|
C | T | 1 | a0001c0001t0003g0171 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1242-931C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7333055 | ||||||
| chrX:7333391
|
T | C | 11 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(8): Show | 11 | HG02055.hp1 HG02559.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1242-595T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7333391 | ||||||
| chrX:7333574
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1242-412C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 9/10 | chrX | 7333574 | ||||||
| chrX:7334393
|
G | A | 12 | a0001c0001t0005g0056a0001c0001t0005g0138a0001c0001t0005g0218others(9): Show | 12 | HG01106.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1363+286G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7334393 | ||||||
| chrX:7334396
|
G | A | 12 | a0001c0001t0005g0056a0001c0001t0005g0138a0001c0001t0005g0218others(9): Show | 12 | HG01106.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1363+289G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7334396 | ||||||
| chrX:7334461
|
C | G | 1 | a0001c0001t0037g0224 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1363+354C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7334461 | ||||||
| chrX:7334841
|
A | G | 1 | a0001c0001t0002g0004 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1363+734A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7334841 | ||||||
| chrX:7334997
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1363+890C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7334997 | ||||||
| chrX:7335131
|
T | G | 1 | a0001c0001t0023g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1363+1024T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7335131 | ||||||
| chrX:7335215
|
C | G | 1 | a0001c0001t0005g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1363+1108C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7335215 | ||||||
| chrX:7335377
|
T | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(158): Show | 163 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.1363+1270T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7335377 | ||||||
| chrX:7335550
|
C | T | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | NA18981.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1363+1443C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7335550 | ||||||
| chrX:7335669
|
G | A | 3 | a0001c0001t0005g0221a0001c0001t0037g0224a0004c0009t0002g0225 | 3 | HG01106.hp1 HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1363+1562G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7335669 | ||||||
| chrX:7336024
|
G | A | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1363+1917G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7336024 | ||||||
| chrX:7336134
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1363+2027A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7336134 | ||||||
| chrX:7336239
|
G | GC | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(131): Show | 136 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.1363+2140dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7336239 | |||||
| chrX:7336239
|
G | GCC | 1 | a0001c0001t0001g0025 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1363+2139_1363+214 others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7336239 | |||||
| chrX:7336440
|
C | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(50): Show | 55 | HG00558.hp2 HG00642.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.1363+2333C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7336440 | ||||||
| chrX:7336611
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1363+2504A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7336611 | ||||||
| chrX:7336775
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0003g0142 | 3 | NA18948.hp1 NA18984.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1363+2668G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7336775 | ||||||
| chrX:7337218
|
G | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(217): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1363+3111G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7337218 | ||||||
| chrX:7337571
|
G | A | 1 | a0001c0001t0005g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1363+3464G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7337571 | ||||||
| chrX:7337791
|
C | T | 1 | a0001c0001t0023g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1363+3684C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7337791 | ||||||
| chrX:7337830
|
CT | C | 1 | a0001c0001t0023g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1363+3724delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7337830 | ||||||
| chrX:7338389
|
A | G | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1363+4282A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7338389 | ||||||
| chrX:7338463
|
T | C | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1363+4356T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7338463 | ||||||
| chrX:7338601
|
C | T | 1 | a0001c0001t0003g0171 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1363+4494C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7338601 | ||||||
| chrX:7338756
|
A | G | 1 | a0001c0001t0040g0227 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1363+4649A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7338756 | ||||||
| chrX:7339666
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1363+5559G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7339666 | ||||||
| chrX:7339871
|
A | G | 12 | a0001c0001t0002g0099a0001c0001t0002g0104a0001c0001t0002g0105others(9): Show | 12 | HG02055.hp1 HG02559.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1363+5764A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7339871 | ||||||
| chrX:7339970
|
T | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0149a0001c0001t0035g0229 | 3 | HG01243.hp1 HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1363+5863T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7339970 | ||||||
| chrX:7340056
|
C | CA | 4 | a0001c0001t0003g0124a0001c0001t0003g0163a0001c0001t0021g0096others(1): Show | 4 | HG01358.hp1 NA19000.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1363+5965dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7340056 | |||||
| chrX:7340056
|
CA | C | 2 | a0001c0001t0001g0060a0001c0001t0013g0033 | 2 | NA19063.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1363+5965delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7340056 | |||||
| chrX:7340146
|
A | C | 12 | a0001c0001t0002g0099a0001c0001t0002g0104a0001c0001t0002g0105others(9): Show | 12 | HG02055.hp1 HG02559.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1363+6039A>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7340146 | ||||||
| chrX:7340665
|
T | TA | 1 | a0001c0001t0005g0138 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1363+6567dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7340665 | |||||
| chrX:7340665
|
TA | T | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1363+6567delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7340665 | |||||
| chrX:7340732
|
C | T | 1 | a0001c0008t0005g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1363+6625C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7340732 | ||||||
| chrX:7340783
|
AC | A | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1363+6678delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7340783 | |||||
| chrX:7340856
|
CG | C | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1363+6752delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7340856 | |||||
| chrX:7340975
|
G | GGT | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1363+6869_1363+687 others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7340975 | |||||
| chrX:7340999
|
G | T | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1363+6892G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7340999 | ||||||
| chrX:7341004
|
T | TG | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1363+6897_1363+689 others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7341004 | ||||||
| chrX:7341039
|
A | AG | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1363+6934dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7341039 | |||||
| chrX:7341046
|
C | T | 2 | a0001c0001t0002g0086a0001c0001t0002g0092 | 2 | HG01255.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1363+6939C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7341046 | ||||||
| chrX:7341048
|
G | GA | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1363+6942dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7341048 | |||||
| chrX:7341111
|
G | GT | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1363+7004_1363+700 others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7341111 | ||||||
| chrX:7341124
|
AT | A | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1363+7019delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7341124 | |||||
| chrX:7341321
|
A | AT | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1363+7216dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7341321 | |||||
| chrX:7341401
|
C | T | 2 | a0001c0001t0002g0182a0001c0001t0002g0206 | 2 | HG00609.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1363+7294C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7341401 | ||||||
| chrX:7341451
|
T | TC | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1363+7346dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7341451 | |||||
| chrX:7341473
|
G | GC | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1363+7371dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7341473 | |||||
| chrX:7341516
|
G | GCA | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1363+7410_1363+741 others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7341516 | |||||
| chrX:7341536
|
C | CT | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1363+7431dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7341536 | |||||
| chrX:7341558
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1363+7451C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7341558 | ||||||
| chrX:7341671
|
C | T | 1 | a0001c0001t0028g0195 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1363+7564C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7341671 | ||||||
| chrX:7341707
|
CT | C | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1363+7602delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7341707 | |||||
| chrX:7341751
|
TC | T | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1363+7648delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7341751 | |||||
| chrX:7341792
|
C | CT | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1363+7696dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7341792 | |||||
| chrX:7341792
|
CT | C | 1 | a0001c0001t0002g0207 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1363+7696delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7341792 | |||||
| chrX:7341818
|
A | AT | 1 | a0001c0001t0002g0189 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1363+7722dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7341818 | |||||
| chrX:7341818
|
AT | A | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1363+7722delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7341818 | |||||
| chrX:7341851
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1363+7744T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7341851 | ||||||
| chrX:7341852
|
G | A | 1 | a0001c0001t0014g0216 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1363+7745G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7341852 | ||||||
| chrX:7342000
|
CG | C | 1 | a0001c0001t0003g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1364-7884delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7342000 | |||||
| chrX:7342004
|
G | GT | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-7881dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7342004 | |||||
| chrX:7342059
|
C | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(132): Show | 137 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.1364-7829C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7342059 | ||||||
| chrX:7342139
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1364-7749C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7342139 | ||||||
| chrX:7342141
|
A | ATTGGGCC | 1 | a0001c0001t0001g0001 | 2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1364-7746_1364-774 others(11): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7342141 | |||||
| chrX:7342146
|
A | T | 1 | a0001c0001t0001g0001 | 2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1364-7742A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7342146 | ||||||
| chrX:7342147
|
G | T | 1 | a0001c0001t0001g0001 | 2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1364-7741G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7342147 | ||||||
| chrX:7342148
|
A | T | 1 | a0001c0001t0001g0001 | 2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1364-7740A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7342148 | ||||||
| chrX:7342151
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1364-7737C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7342151 | ||||||
| chrX:7342152
|
TAGGCACT others(217): Show |
T | 1 | a0001c0001t0001g0001 | 2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1364-7735_1364-751 others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7342152 | ||||||
| chrX:7342193
|
G | GC | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-7693dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7342193 | |||||
| chrX:7342395
|
T | TC | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-7492dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7342395 | |||||
| chrX:7342511
|
TG | T | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-7374delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7342511 | |||||
| chrX:7342579
|
T | TC | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-7307dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7342579 | |||||
| chrX:7342615
|
T | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(144): Show | 149 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(146): Show |
intron_variant | MODIFIER | c.1364-7273T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7342615 | ||||||
| chrX:7342692
|
A | AG | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-7191dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7342692 | |||||
| chrX:7342698
|
T | C | 12 | a0001c0001t0002g0099a0001c0001t0002g0104a0001c0001t0002g0105others(9): Show | 12 | HG02055.hp1 HG02559.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1364-7190T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7342698 | ||||||
| chrX:7342705
|
T | TA | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-7182dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7342705 | |||||
| chrX:7342749
|
C | CT | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-7137dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7342749 | |||||
| chrX:7342764
|
CT | C | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-7120delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7342764 | |||||
| chrX:7342780
|
A | AT | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-7107dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7342780 | |||||
| chrX:7342800
|
C | T | 4 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1364-7088C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7342800 | ||||||
| chrX:7342843
|
TG | T | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-7042delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7342843 | |||||
| chrX:7342880
|
A | T | 1 | a0001c0001t0018g0141 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1364-7008A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7342880 | ||||||
| chrX:7342922
|
T | TG | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-6964dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7342922 | |||||
| chrX:7343033
|
G | T | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1364-6855G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7343033 | ||||||
| chrX:7343126
|
GA | G | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-6758delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7343126 | |||||
| chrX:7343186
|
C | G | 1 | a0001c0001t0013g0051 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1364-6702C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7343186 | ||||||
| chrX:7343248
|
G | GC | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-6640_1364-663 others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7343248 | ||||||
| chrX:7343467
|
C | T | 1 | a0003c0003t0003g0147 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1364-6421C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7343467 | ||||||
| chrX:7343612
|
A | AG | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-6275dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7343612 | |||||
| chrX:7343685
|
G | GA | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-6203_1364-620 others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7343685 | ||||||
| chrX:7343768
|
C | CCT | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-6118_1364-611 others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7343768 | |||||
| chrX:7343816
|
A | AG | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-6071dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7343816 | |||||
| chrX:7343874
|
C | CG | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-6011dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7343874 | |||||
| chrX:7343893
|
C | CT | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-5993dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7343893 | |||||
| chrX:7343962
|
T | TG | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-5924dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7343962 | |||||
| chrX:7344032
|
G | GA | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-5855dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7344032 | |||||
| chrX:7344076
|
T | G | 1 | a0001c0001t0023g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1364-5812T>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7344076 | ||||||
| chrX:7344094
|
T | TC | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-5793dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7344094 | |||||
| chrX:7344138
|
T | TG | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-5748dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7344138 | |||||
| chrX:7344166
|
GC | G | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-5719delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7344166 | |||||
| chrX:7344188
|
GC | G | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-5697delC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7344188 | |||||
| chrX:7344333
|
C | CT | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-5554dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7344333 | |||||
| chrX:7344417
|
A | AG | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-5470dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7344417 | |||||
| chrX:7344453
|
T | TG | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-5430dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7344453 | |||||
| chrX:7344489
|
G | T | 12 | a0001c0001t0002g0099a0001c0001t0002g0104a0001c0001t0002g0105others(9): Show | 12 | HG02055.hp1 HG02559.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1364-5399G>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7344489 | ||||||
| chrX:7344501
|
C | G | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1364-5387C>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7344501 | ||||||
| chrX:7344565
|
TG | T | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-5320delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7344565 | |||||
| chrX:7344685
|
C | T | 1 | a0001c0001t0005g0138 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1364-5203C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7344685 | ||||||
| chrX:7344709
|
T | TTTG | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-5178_1364-517 others(7): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7344709 | |||||
| chrX:7344756
|
T | TG | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-5129dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7344756 | |||||
| chrX:7344768
|
A | AG | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-5116dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7344768 | |||||
| chrX:7344778
|
A | AG | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-5107dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7344778 | |||||
| chrX:7344843
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1364-5045C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7344843 | ||||||
| chrX:7344862
|
T | TG | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-5024dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7344862 | |||||
| chrX:7344955
|
TG | T | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-4931delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7344955 | |||||
| chrX:7344966
|
G | A | 6 | a0001c0001t0003g0151a0001c0001t0003g0163a0001c0001t0003g0171others(3): Show | 6 | HG02040.hp1 NA18747.hp1 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.1364-4922G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7344966 | ||||||
| chrX:7345104
|
G | GT | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-4782dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7345104 | |||||
| chrX:7345118
|
G | GT | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-4770_1364-476 others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7345118 | ||||||
| chrX:7345158
|
A | AG | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-4728dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7345158 | |||||
| chrX:7345240
|
AG | A | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-4645delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7345240 | |||||
| chrX:7345290
|
T | C | 1 | a0001c0001t0019g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1364-4598T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7345290 | ||||||
| chrX:7345420
|
G | GT | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-4467dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7345420 | |||||
| chrX:7345436
|
T | TA | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-4449dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7345436 | |||||
| chrX:7345477
|
T | TC | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-4409dupC | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7345477 | |||||
| chrX:7345493
|
AG | A | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-4393delG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7345493 | |||||
| chrX:7345618
|
T | C | 4 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(1): Show | 4 | NA18980.hp2 NA18981.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.1364-4270T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7345618 | ||||||
| chrX:7345633
|
C | T | 1 | a0001c0001t0024g0211 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1364-4255C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7345633 | ||||||
| chrX:7345645
|
G | GT | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-4243_1364-424 others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7345645 | ||||||
| chrX:7345760
|
A | AG | 1 | a0001c0001t0021g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1364-4126dupG | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7345760 | |||||
| chrX:7346227
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1364-3661T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7346227 | ||||||
| chrX:7346458
|
T | TA | 4 | a0001c0001t0002g0186a0001c0001t0002g0196a0001c0001t0002g0212others(1): Show | 4 | HG00673.hp1 HG02258.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1364-3408dupA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7346458 | |||||
| chrX:7346458
|
TA | T | 38 | a0001c0001t0001g0024a0001c0001t0001g0047a0001c0001t0001g0054others(35): Show | 38 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.1364-3408delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7346458 | |||||
| chrX:7346458
|
TAA | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(136): Show | 141 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1364-3409_1364-340 others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7346458 | |||||
| chrX:7346458
|
TAAA | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0003g0109others(2): Show | 5 | HG00639.hp1 HG01074.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.1364-3410_1364-340 others(7): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7346458 | |||||
| chrX:7346605
|
G | C | 1 | a0001c0001t0001g0019 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1364-3283G>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7346605 | ||||||
| chrX:7346658
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1364-3230C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7346658 | ||||||
| chrX:7346679
|
TA | T | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1364-3204delA | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7346679 | |||||
| chrX:7347060
|
C | A | 1 | a0001c0001t0001g0054 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1364-2828C>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7347060 | ||||||
| chrX:7347228
|
A | G | 1 | a0001c0001t0030g0038 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1364-2660A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7347228 | ||||||
| chrX:7347338
|
A | G | 1 | a0001c0001t0019g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1364-2550A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7347338 | ||||||
| chrX:7347887
|
A | T | 1 | a0001c0001t0031g0018 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1364-2001A>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7347887 | ||||||
| chrX:7347901
|
C | T | 1 | a0001c0001t0002g0212 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1364-1987C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7347901 | ||||||
| chrX:7347902
|
G | A | 2 | a0001c0001t0003g0157a0001c0001t0003g0162 | 2 | HG03017.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1364-1986G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7347902 | ||||||
| chrX:7348158
|
C | T | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(158): Show | 163 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.1364-1730C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7348158 | ||||||
| chrX:7348384
|
G | A | 1 | a0001c0001t0002g0206 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1364-1504G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7348384 | ||||||
| chrX:7348739
|
T | C | 11 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0003g0111others(8): Show | 11 | HG02027.hp1 HG02132.hp1 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.1364-1149T>C | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7348739 | ||||||
| chrX:7348789
|
A | G | 1 | a0001c0001t0003g0169 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1364-1099A>G | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7348789 | ||||||
| chrX:7349145
|
C | CT | 8 | a0001c0001t0002g0086a0001c0001t0002g0092a0001c0001t0002g0105others(5): Show | 8 | HG01255.hp1 HG01361.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.1364-723dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7349145 | |||||
| chrX:7349145
|
CT | C | 19 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0042others(16): Show | 19 | HG01069.hp1 HG01074.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.1364-723delT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7349145 | |||||
| chrX:7349229
|
TCA | T | 1 | a0001c0001t0001g0016 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1364-658_1364-657d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7349229 | ||||||
| chrX:7349235
|
C | T | 1 | a0001c0001t0003g0111 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1364-653C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7349235 | ||||||
| chrX:7349315
|
CCTTT | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0037a0001c0001t0001g0063 | 3 | HG03195.hp1 NA18988.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1364-572_1364-569d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7349315 | ||||||
| chrX:7349315
|
CCTTTT | C | 16 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0022others(13): Show | 16 | HG01074.hp1 HG01243.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1364-572_1364-568d others(7): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7349315 | ||||||
| chrX:7349315
|
CCTTTTT | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(48): Show | 53 | HG00558.hp2 HG00621.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1364-572_1364-567d others(8): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7349315 | ||||||
| chrX:7349315
|
CCTTTTTT | C | 69 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(66): Show | 69 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1364-572_1364-566d others(9): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7349315 | ||||||
| chrX:7349315
|
CCTTTTTT others(1): Show |
C | 4 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 4 | HG01109.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1364-572_1364-565d others(10): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7349315 | ||||||
| chrX:7349315
|
CCTTTTTT others(6): Show |
C | 1 | a0002c0002t0027g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1364-572_1364-560d others(15): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7349315 | ||||||
| chrX:7349315
|
CCTTTTTT others(15): Show |
C | 1 | a0001c0001t0003g0142 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1364-572_1364-551d others(24): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7349315 | ||||||
| chrX:7349316
|
C | CT | 27 | a0001c0001t0002g0004a0001c0001t0002g0080a0001c0001t0002g0086others(24): Show | 27 | HG00323.hp1 HG00323.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1364-535dupT | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7349316 | |||||
| chrX:7349316
|
C | CTT | 23 | a0001c0001t0002g0092a0001c0001t0002g0095a0001c0001t0002g0187others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1364-536_1364-535d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7349316 | |||||
| chrX:7349316
|
C | CTTT | 10 | a0001c0001t0002g0036a0001c0001t0002g0083a0001c0001t0002g0179others(7): Show | 10 | HG00558.hp1 HG00673.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1364-537_1364-535d others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7349316 | |||||
| chrX:7349316
|
C | CTTTT | 3 | a0001c0001t0002g0182a0001c0001t0004g0084a0001c0001t0040g0227 | 3 | HG03471.hp1 NA18975.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1364-538_1364-535d others(6): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7349316 | |||||
| chrX:7349316
|
C | CTTTTT | 1 | a0001c0001t0038g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1364-539_1364-535d others(7): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7349316 | |||||
| chrX:7349316
|
CTT | C | 1 | a0001c0001t0002g0217 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1364-536_1364-535d others(4): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7349316 | |||||
| chrX:7349316
|
CTTT | C | 1 | a0001c0001t0028g0195 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1364-537_1364-535d others(5): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7349316 | |||||
| chrX:7349316
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0002g0135a0001c0001t0010g0100a0001c0001t0010g0145 | 3 | HG02055.hp1 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1364-546_1364-535d others(14): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7349316 | |||||
| chrX:7349316
|
CTTTTTTT others(6): Show |
C | 9 | a0001c0001t0002g0099a0001c0001t0002g0104a0001c0001t0002g0105others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1364-547_1364-535d others(15): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7349316 | |||||
| chrX:7349316
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0002g0188 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1364-552_1364-535d others(20): Show |
STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 7349316 | |||||
| chrX:7349431
|
G | A | 9 | a0001c0001t0005g0056a0001c0001t0005g0138a0001c0001t0005g0218others(6): Show | 9 | HG01074.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1364-457G>A | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7349431 | ||||||
| chrX:7349525
|
C | T | 1 | a0001c0001t0024g0211 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1364-363C>T | STS | ENSG00000101846.9 | transcript | ENST00000674429.1 | protein_coding | 10/10 | chrX | 7349525 |