| geneid | 8239 |
|---|---|
| ensemblid | ENSG00000124486.15 |
| hgncid | 12632 |
| symbol | USP9X |
| name | ubiquitin specific peptidase 9 X-linked |
| refseq_nuc | NM_001039591.3 |
| refseq_prot | NP_001034680.2 |
| ensembl_nuc | ENST00000378308.7 |
| ensembl_prot | ENSP00000367558.2 |
| mane_status | MANE Select |
| chr | chrX |
| start | 41085445 |
| end | 41236579 |
| strand | + |
| ver | v1.2 |
| region | chrX:41085445-41236579 |
| region5000 | chrX:41080445-41241579 |
| regionname0 | USP9X_chrX_41085445_41236579 |
| regionname5000 | USP9X_chrX_41080445_41241579 |
| 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 | 2554 | 285 | 66 | 54 | 126 | 9 | 28 | 95 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0002 | 0/0 | 2554 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0003 | 0/0 | 1369 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0004 | 0/0 | 1629 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0005 | 0/0 | 2554 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0006 | 0/0 | 397 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0007 | 0/0 | 2554 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0008 | 0/0 | 36 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| 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 | 7665 | 267 | 51 | 54 | 123 | 9 | 28 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| c0002 | 0/0 | 7665 | 11 | 11 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| c0003 | 0/0 | 7665 | 3 | 0 | 0 | 3 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| c0004 | 0/0 | 7665 | 3 | 3 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| c0005 | 0/0 | 7665 | 2 | 2 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| c0006 | 0/0 | 7667 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| c0007 | 0/0 | 7664 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| c0008 | 0/0 | 7665 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| c0009 | 0/0 | 7663 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| c0010 | 0/0 | 7666 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| c0011 | 0/0 | 7665 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| c0012 | 0/0 | 7665 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| 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 | 0/1 | 4879 | 97 | 15 | 17 | 52 | 4 | 8 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0002 | 1/0 | 4879 | 83 | 32 | 10 | 35 | 1 | 4 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0003 | 0/0 | 4880 | 31 | 7 | 2 | 14 | 1 | 7 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0004 | 0/0 | 4880 | 22 | 0 | 10 | 12 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0005 | 0/0 | 4879 | 13 | 1 | 1 | 6 | 0 | 5 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0006 | 0/0 | 4878 | 6 | 0 | 1 | 4 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0007 | 0/0 | 4879 | 5 | 2 | 1 | 0 | 1 | 1 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0008 | 0/0 | 4879 | 5 | 0 | 4 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0009 | 0/0 | 4879 | 3 | 0 | 2 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0010 | 0/0 | 4879 | 2 | 0 | 2 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0011 | 0/0 | 4881 | 2 | 2 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0012 | 0/0 | 4880 | 2 | 2 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0013 | 0/0 | 4879 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0014 | 0/0 | 4879 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0015 | 0/0 | 4878 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0016 | 0/0 | 4878 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0017 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0018 | 0/0 | 4879 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0019 | 0/0 | 4879 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0020 | 0/0 | 4880 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0021 | 0/0 | 4879 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0022 | 0/0 | 4879 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0023 | 0/0 | 4879 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0024 | 0/0 | 4877 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0025 | 0/0 | 4880 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0026 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0027 | 0/0 | 4880 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0028 | 0/0 | 4879 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0029 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0030 | 0/0 | 4879 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0031 | 0/0 | 4880 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0032 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0033 | 0/0 | 4880 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| t0034 | 0/0 | 4877 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0005 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0125 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| 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 | 7665 | 267 | 51 | 54 | 123 | 9 | 28 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0002 | 0/0 | 7665 | 11 | 11 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0003 | 0/0 | 7665 | 3 | 0 | 0 | 3 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0004 | 0/0 | 7665 | 3 | 3 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0008 | 0/0 | 7665 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0002c0005 | 0/0 | 7665 | 2 | 2 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0003c0010 | 0/0 | 7666 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0004c0009 | 0/0 | 7663 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0005c0011 | 0/0 | 7665 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0006c0007 | 0/0 | 7664 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0007c0012 | 0/0 | 7665 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0008c0006 | 0/0 | 7667 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 12543 | 92 | 14 | 17 | 48 | 4 | 8 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0002 | 1/0 | 12543 | 67 | 17 | 10 | 34 | 1 | 4 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0003 | 0/0 | 12544 | 31 | 7 | 2 | 14 | 1 | 7 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0004 | 0/0 | 12544 | 22 | 0 | 10 | 12 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0005 | 0/0 | 12543 | 13 | 1 | 1 | 6 | 0 | 5 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0006 | 0/0 | 12542 | 5 | 0 | 1 | 3 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0007 | 0/0 | 12543 | 5 | 2 | 1 | 0 | 1 | 1 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0008 | 0/0 | 12543 | 5 | 0 | 4 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0009 | 0/0 | 12543 | 3 | 0 | 2 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0010 | 0/0 | 12543 | 2 | 0 | 2 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0012 | 0/0 | 12544 | 2 | 2 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0013 | 0/0 | 12543 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0014 | 0/0 | 12543 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0015 | 0/0 | 12542 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0016 | 0/0 | 12542 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0017 | 0/0 | 12542 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0018 | 0/0 | 12543 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0019 | 0/0 | 12543 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0022 | 0/0 | 12543 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0023 | 0/0 | 12543 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0024 | 0/0 | 12541 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0025 | 0/0 | 12544 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0026 | 0/0 | 12542 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0027 | 0/0 | 12544 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0028 | 0/0 | 12543 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0029 | 0/0 | 12545 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0030 | 0/0 | 12543 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0031 | 0/0 | 12544 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0032 | 0/0 | 12542 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0033 | 0/0 | 12544 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0001t0034 | 0/0 | 12541 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0002t0002 | 0/0 | 12543 | 10 | 10 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0002t0021 | 0/0 | 12543 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0003t0001 | 0/0 | 12543 | 3 | 0 | 0 | 3 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0004t0002 | 0/0 | 12543 | 3 | 3 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0001c0008t0002 | 0/0 | 12543 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0002c0005t0011 | 0/0 | 12545 | 2 | 2 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0003c0010t0002 | 0/0 | 12544 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0004c0009t0006 | 0/0 | 12540 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0005c0011t0002 | 0/0 | 12543 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0006c0007t0020 | 0/0 | 12543 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0007c0012t0001 | 0/0 | 12543 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| a0008c0006t0001 | 0/0 | 12545 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | copy fasta | chrX | 41080445 | 41241579 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0125 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0005 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0006g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0006g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0007g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0007g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0007g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0008g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0008g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0008g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0008g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0008g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0009g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0009g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0009g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0010g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0010g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0012g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0012g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0013g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0014g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0015g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0016g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0017g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0018g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0019g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0022g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0023g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0024g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0025g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0026g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0027g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0028g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0029g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0030g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0031g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0032g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0033g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0001t0034g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0002t0021g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0004t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0004t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0004t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0001c0008t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0002c0005t0011g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0002c0005t0011g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0003c0010t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0004c0009t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0005c0011t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0006c0007t0020g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0007c0012t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| a0008c0006t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0009 | g0025 | EUR | GBR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | GBR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | GBR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0017 | EUR | FIN | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0280 | EUR | FIN | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0019 | EUR | FIN | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | CHS | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0252 | EAS | CHS | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | CHS | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | CHS | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | CHS | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00735 | hp2 | a0001 | c0001 | t0009 | g0061 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00738 | hp1 | a0001 | c0001 | t0010 | g0157 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00741 | hp1 | a0001 | c0001 | t0010 | g0156 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG00741 | hp2 | a0001 | c0001 | t0009 | g0233 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01070 | hp1 | a0001 | c0001 | t0006 | g0123 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01070 | hp2 | a0001 | c0001 | t0008 | g0142 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0242 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01099 | hp1 | a0001 | c0001 | t0016 | g0185 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0257 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01168 | hp1 | a0001 | c0001 | t0007 | g0020 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01168 | hp2 | a0001 | c0001 | t0008 | g0135 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0265 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01192 | hp1 | a0001 | c0001 | t0008 | g0136 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01243 | hp1 | a0001 | c0001 | t0033 | g0240 | AMR | PUR | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0272 | AMR | CLM | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01258 | hp1 | a0001 | c0001 | t0018 | g0032 | AMR | CLM | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01261 | hp1 | a0001 | c0001 | t0014 | g0279 | AMR | CLM | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0264 | AMR | CLM | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01433 | hp1 | a0001 | c0001 | t0008 | g0103 | AMR | CLM | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0245 | AMR | CLM | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0128 | EUR | IBS | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0122 | AFR | ACB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0251 | AMR | PEL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0258 | AMR | PEL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0270 | AMR | PEL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0262 | AMR | PEL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0281 | AMR | PEL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02040 | hp1 | a0001 | c0001 | t0024 | g0234 | EAS | KHV | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0286 | EAS | KHV | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | ACB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0091 | AMR | PEL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CDX | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | CDX | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CDX | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0118 | AFR | ACB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02280 | hp2 | a0001 | c0001 | t0012 | g0082 | AFR | ACB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0278 | AMR | PEL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0119 | AFR | ACB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | KHV | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0066 | SAS | PJL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0276 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0254 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0287 | SAS | PJL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0289 | SAS | PJL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0121 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02723 | hp1 | a0001 | c0001 | t0023 | g0022 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02723 | hp2 | a0001 | c0004 | t0002 | g0178 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02895 | hp1 | a0001 | c0001 | t0032 | g0222 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02896 | hp1 | a0001 | c0004 | t0002 | g0177 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02922 | hp1 | a0001 | c0001 | t0022 | g0014 | AFR | ESN | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0045 | AFR | ESN | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0174 | AFR | ESN | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0052 | SAS | PJL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03041 | hp1 | a0005 | c0011 | t0002 | g0117 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03098 | hp1 | a0001 | c0001 | t0019 | g0018 | AFR | MSL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0175 | AFR | ESN | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03195 | hp1 | a0001 | c0001 | t0028 | g0179 | AFR | ESN | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03209 | hp1 | a0001 | c0001 | t0027 | g0104 | AFR | MSL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0044 | AFR | MSL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03453 | hp1 | a0007 | c0012 | t0001 | g0105 | AFR | MSL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | MSL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0215 | AFR | MSL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03490 | hp1 | a0001 | c0001 | t0008 | g0137 | SAS | PJL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03491 | hp2 | a0001 | c0001 | t0007 | g0043 | SAS | PJL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0120 | AFR | GWD | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03579 | hp1 | a0001 | c0008 | t0002 | g0216 | AFR | MSL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0290 | SAS | PJL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0282 | SAS | STU | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03704 | hp1 | a0001 | c0001 | t0015 | g0021 | SAS | PJL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0292 | SAS | PJL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0284 | SAS | BEB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | STU | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0253 | SAS | BEB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0054 | SAS | BEB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG04199 | hp1 | a0001 | c0001 | t0025 | g0133 | SAS | STU | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0080 | SAS | STU | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | STU | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | YRI | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18612 | hp1 | a0001 | c0001 | t0026 | g0166 | EAS | CHB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | CHB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0238 | AFR | YRI | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18906 | hp2 | a0001 | c0002 | t0021 | g0195 | AFR | YRI | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18939 | hp2 | a0001 | c0001 | t0005 | g0063 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18941 | hp1 | a0001 | c0001 | t0034 | g0001 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18946 | hp2 | a0001 | c0001 | t0006 | g0148 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18948 | hp1 | a0001 | c0001 | t0006 | g0165 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18954 | hp2 | a0001 | c0003 | t0001 | g0130 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18957 | hp1 | a0001 | c0003 | t0001 | g0150 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0064 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18973 | hp2 | a0001 | c0001 | t0005 | g0090 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18981 | hp2 | a0003 | c0010 | t0002 | g0074 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18982 | hp1 | a0001 | c0003 | t0001 | g0151 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | LWK | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0196 | AFR | LWK | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0241 | AFR | LWK | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19063 | hp1 | a0001 | c0001 | t0031 | g0273 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19067 | hp1 | a0006 | c0007 | t0020 | g0098 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19072 | hp1 | a0004 | c0009 | t0006 | g0116 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19078 | hp1 | a0008 | c0006 | t0001 | g0002 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19087 | hp2 | a0001 | c0001 | t0029 | g0077 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19091 | hp1 | a0001 | c0001 | t0017 | g0023 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | YRI | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA19240 | hp2 | a0002 | c0005 | t0011 | g0235 | AFR | YRI | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0239 | AFR | ASW | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | ASW | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | TSI | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0051 | SAS | GIH | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | CLM | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | ACB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02109 | hp2 | a0001 | c0001 | t0030 | g0275 | AFR | ACB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02486 | hp1 | a0001 | c0001 | t0012 | g0107 | AFR | ACB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02559 | hp1 | a0001 | c0001 | t0013 | g0180 | AFR | ACB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0176 | AFR | ACB | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | MSL | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG06807 | hp1 | a0002 | c0005 | t0011 | g0236 | AFR | USA | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | USA | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA20300 | hp1 | a0001 | c0004 | t0002 | g0211 | AFR | USA | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0092 | AFR | USA | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0125 | REF | REF | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0005 | REF | REF | USP9X_chrX_41080445_41241579 | USP9X | chrX | 41080445 | 41241579 |
| 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:41123703
|
G | GC | 1 | a0008 | 1 | NA19078.hp1 | frameshift_variant | HIGH | c.82dupC | p.Leu28fs | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/45 | 906/12543 | 83/7665 | 28/2554 | INFO_REALIGN_3_PRIME | chrX | 41123703 | |
| chrX:41131500
|
G | T | 1 | a0002 | 2 | HG06807.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.286G>T | p.Val96Leu | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/45 | 1109/12543 | 286/7665 | 96/2554 | chrX | 41131500 | ||
| chrX:41140696
|
A | G | 1 | a0007 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.695A>G | p.Asn232Ser | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 7/45 | 1518/12543 | 695/7665 | 232/2554 | chrX | 41140696 | ||
| chrX:41141427
|
TG | T | 1 | a0006 | 1 | NA19067.hp1 | frameshift_variant&splice_region_variant | HIGH | c.1159delG | p.Ala387fs | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 9/45 | 1982/12543 | 1159/7665 | 387/2554 | INFO_REALIGN_3_PRIME | chrX | 41141427 | |
| chrX:41150982
|
A | T | 1 | a0005 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.1688A>T | p.Asp563Val | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/45 | 2511/12543 | 1688/7665 | 563/2554 | chrX | 41150982 | ||
| chrX:41196307
|
T | TG | 1 | a0008 | 1 | NA19078.hp1 | frameshift_variant | HIGH | c.4037dupG | p.His1347fs | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 27/45 | 4861/12543 | 4038/7665 | 1346/2554 | INFO_REALIGN_3_PRIME | chrX | 41196307 | |
| chrX:41196331
|
T | TC | 1 | a0003 | 1 | NA18981.hp2 | frameshift_variant | HIGH | c.4059dupC | p.Ile1354fs | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 27/45 | 4883/12543 | 4060/7665 | 1354/2554 | INFO_REALIGN_3_PRIME | chrX | 41196331 | |
| chrX:41196720
|
T | A | 1 | a0003 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.4215T>A | p.Asp1405Glu | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 28/45 | 5038/12543 | 4215/7665 | 1405/2554 | chrX | 41196720 | ||
| chrX:41197462
|
G | GA | 1 | a0003 | 1 | NA18981.hp2 | frameshift_variant | HIGH | c.4338dupA | p.Phe1447fs | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 29/45 | 5162/12543 | 4339/7665 | 1447/2554 | INFO_REALIGN_3_PRIME | chrX | 41197462 | |
| chrX:41198647
|
TG | T | 1 | a0003 | 1 | NA18981.hp2 | frameshift_variant | HIGH | c.4502delG | p.Gly1501fs | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 30/45 | 5325/12543 | 4502/7665 | 1501/2554 | INFO_REALIGN_3_PRIME | chrX | 41198647 | |
| chrX:41205314
|
TC | T | 1 | a0004 | 1 | NA19072.hp1 | frameshift_variant | HIGH | c.4839delC | p.Arg1614fs | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/45 | 5662/12543 | 4839/7665 | 1613/2554 | INFO_REALIGN_3_PRIME | chrX | 41205314 | |
| chrX:41214670
|
AG | A | 1 | a0004 | 1 | NA19072.hp1 | frameshift_variant | HIGH | c.5294delG | p.Gly1765fs | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 34/45 | 6117/12543 | 5294/7665 | 1765/2554 | INFO_REALIGN_3_PRIME | chrX | 41214670 | |
| chrX:41214709
|
G | T | 1 | a0004 | 1 | NA19072.hp1 | missense_variant&splice_region_variant | MODERATE | c.5331G>T | p.Lys1777Asn | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 34/45 | 6154/12543 | 5331/7665 | 1777/2554 | chrX | 41214709 |
| 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:41196356
|
G | A | 3 | a0001c0002a0001c0008a0005c0011 | 13 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(10): Show |
synonymous_variant | LOW | c.4083G>A | p.Leu1361Leu | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 27/45 | 4906/12543 | 4083/7665 | 1361/2554 | chrX | 41196356 | ||
| chrX:41196660
|
C | T | 1 | a0001c0008 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.4155C>T | p.Tyr1385Tyr | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 28/45 | 4978/12543 | 4155/7665 | 1385/2554 | chrX | 41196660 | ||
| chrX:41201205
|
C | T | 1 | a0001c0004 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.4749C>T | p.Asn1583Asn | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/45 | 5572/12543 | 4749/7665 | 1583/2554 | chrX | 41201205 | ||
| chrX:41201268
|
G | A | 2 | a0001c0003a0008c0006 | 4 | NA18954.hp2 NA18957.hp1 NA18982.hp1 others(1): Show |
synonymous_variant | LOW | c.4812G>A | p.Lys1604Lys | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/45 | 5635/12543 | 4812/7665 | 1604/2554 | chrX | 41201268 | ||
| chrX:41216285
|
A | G | 1 | a0002c0005 | 2 | HG06807.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.5718A>G | p.Thr1906Thr | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 35/45 | 6541/12543 | 5718/7665 | 1906/2554 | chrX | 41216285 |
| 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:41085481
|
C | A | 1 | a0001c0001t0013 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-787C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/45 | 38148 | chrX | 41085481 | |||||
| chrX:41085587
|
TC | T | 1 | a0001c0001t0034 | 1 | NA18941.hp1 | 5_prime_UTR_variant | MODIFIER | c.-678delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/45 | 38039 | INFO_REALIGN_3_PRIME | chrX | 41085587 | ||||
| chrX:41085599
|
CG | C | 1 | a0001c0001t0014 | 1 | HG01261.hp1 | 5_prime_UTR_variant | MODIFIER | c.-666delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/45 | 38027 | INFO_REALIGN_3_PRIME | chrX | 41085599 | ||||
| chrX:41085795
|
A | AC | 1 | a0001c0001t0014 | 1 | HG01261.hp1 | 5_prime_UTR_variant | MODIFIER | c.-471dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/45 | 37831 | INFO_REALIGN_3_PRIME | chrX | 41085795 | ||||
| chrX:41085942
|
C | T | 1 | a0001c0001t0033 | 1 | HG01243.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-326C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/45 | chrX | 41085942 | ||||||
| chrX:41086060
|
G | A | 2 | a0001c0001t0005a0001c0001t0015 | 14 | HG02148.hp1 HG02602.hp1 HG03017.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-208G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/45 | 37569 | chrX | 41086060 | |||||
| chrX:41232688
|
A | G | 1 | a0001c0001t0008 | 5 | HG01070.hp2 HG01168.hp2 HG01192.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*164A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 164 | chrX | 41232688 | |||||
| chrX:41232933
|
GA | G | 1 | a0001c0001t0032 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*421delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 421 | INFO_REALIGN_3_PRIME | chrX | 41232933 | ||||
| chrX:41233194
|
G | C | 1 | a0001c0001t0004 | 22 | HG00423.hp1 HG00597.hp2 HG01074.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*670G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 670 | chrX | 41233194 | |||||
| chrX:41233411
|
G | A | 1 | a0001c0001t0007 | 5 | HG00280.hp1 HG01168.hp1 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*887G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 887 | chrX | 41233411 | |||||
| chrX:41233595
|
G | A | 1 | a0001c0001t0010 | 2 | HG00738.hp1 HG00741.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1071G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 1071 | chrX | 41233595 | |||||
| chrX:41234018
|
G | GT | 1 | a0001c0001t0012 | 2 | HG02280.hp2 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1504dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 1505 | INFO_REALIGN_3_PRIME | chrX | 41234018 | ||||
| chrX:41234045
|
C | CT | 6 | a0001c0001t0003a0001c0001t0004a0001c0001t0027others(3): Show | 57 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1536dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 1537 | INFO_REALIGN_3_PRIME | chrX | 41234045 | ||||
| chrX:41234045
|
C | CTT | 2 | a0001c0001t0029a0002c0005t0011 | 3 | HG06807.hp1 NA19087.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1535_*1536dupTT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 1537 | INFO_REALIGN_3_PRIME | chrX | 41234045 | ||||
| chrX:41234045
|
CT | C | 4 | a0001c0001t0006a0001c0001t0015a0001c0001t0016others(1): Show | 8 | HG01070.hp1 HG01099.hp1 HG01515.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1536delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 1536 | INFO_REALIGN_3_PRIME | chrX | 41234045 | ||||
| chrX:41234061
|
A | T | 8 | a0001c0001t0003a0001c0001t0004a0001c0001t0013others(5): Show | 60 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1537A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 1537 | chrX | 41234061 | |||||
| chrX:41234160
|
A | T | 15 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(12): Show | 117 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1636A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 1636 | chrX | 41234160 | |||||
| chrX:41234685
|
C | T | 1 | a0001c0001t0023 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2161C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 2161 | chrX | 41234685 | |||||
| chrX:41234879
|
AT | A | 1 | a0001c0001t0017 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2358delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 2358 | INFO_REALIGN_3_PRIME | chrX | 41234879 | ||||
| chrX:41235103
|
C | G | 1 | a0001c0001t0022 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2579C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 2579 | chrX | 41235103 | |||||
| chrX:41235211
|
GA | G | 1 | a0001c0001t0026 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2690delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 2690 | INFO_REALIGN_3_PRIME | chrX | 41235211 | ||||
| chrX:41235214
|
A | G | 1 | a0001c0002t0021 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2690A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 2690 | chrX | 41235214 | |||||
| chrX:41235214
|
AGT | A | 1 | a0001c0001t0024 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2692_*2693delTG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 2692 | INFO_REALIGN_3_PRIME | chrX | 41235214 | ||||
| chrX:41235425
|
A | G | 1 | a0001c0001t0016 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2901A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 2901 | chrX | 41235425 | |||||
| chrX:41235596
|
A | C | 1 | a0001c0001t0031 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3072A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 3072 | chrX | 41235596 | |||||
| chrX:41235635
|
G | A | 1 | a0001c0001t0009 | 3 | HG00099.hp1 HG00735.hp2 HG00741.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3111G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 3111 | chrX | 41235635 | |||||
| chrX:41235670
|
T | G | 1 | a0001c0001t0018 | 1 | HG01258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3146T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 3146 | chrX | 41235670 | |||||
| chrX:41235701
|
GT | G | 1 | a0001c0001t0030 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3187delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 3187 | INFO_REALIGN_3_PRIME | chrX | 41235701 | ||||
| chrX:41235889
|
G | A | 1 | a0001c0001t0019 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3365G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 3365 | chrX | 41235889 | |||||
| chrX:41236142
|
T | C | 1 | a0002c0005t0011 | 2 | HG06807.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3618T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 3618 | chrX | 41236142 | |||||
| chrX:41236167
|
G | GA | 1 | a0001c0001t0025 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3653dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 3654 | INFO_REALIGN_3_PRIME | chrX | 41236167 | ||||
| chrX:41236386
|
C | CG | 1 | a0006c0007t0020 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3867dupG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 45/45 | 3868 | INFO_REALIGN_3_PRIME | chrX | 41236386 |
| 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:41086108
|
CG | C | 1 | a0001c0001t0034g0001 | 1 | NA18941.hp1 | splice_donor_variant&intron_variant | HIGH | c.-159+1delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41086108 | |||||
| chrX:41086119
|
C | A | 1 | a0001c0001t0034g0001 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-159+10C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41086119 | ||||||
| chrX:41086157
|
G | C | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-159+48G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41086157 | ||||||
| chrX:41086158
|
C | G | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-159+49C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41086158 | ||||||
| chrX:41086185
|
AG | A | 14 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(11): Show | 14 | HG00323.hp1 HG02004.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-159+82delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41086185 | |||||
| chrX:41086244
|
T | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | NA18951.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.-159+135T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41086244 | ||||||
| chrX:41086264
|
GC | G | 1 | a0001c0001t0014g0279 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-159+158delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41086264 | |||||
| chrX:41086369
|
C | CCCTCCCC others(2): Show |
2 | a0001c0001t0003g0280a0001c0001t0003g0281 | 2 | HG00323.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-159+270_-159+278d others(11): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41086369 | |||||
| chrX:41086442
|
G | GC | 1 | a0001c0001t0014g0279 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-159+340dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41086442 | |||||
| chrX:41086515
|
C | G | 59 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-159+406C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41086515 | ||||||
| chrX:41086597
|
G | C | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-159+488G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41086597 | ||||||
| chrX:41086598
|
C | G | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-159+489C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41086598 | ||||||
| chrX:41086624
|
C | T | 1 | a0001c0001t0004g0278 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-159+515C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41086624 | ||||||
| chrX:41086743
|
C | T | 1 | a0001c0001t0009g0233 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-159+634C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41086743 | ||||||
| chrX:41087031
|
A | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0109others(130): Show | 133 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.-159+922A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41087031 | ||||||
| chrX:41087082
|
C | T | 292 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.-159+973C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41087082 | ||||||
| chrX:41087141
|
CT | C | 1 | a0001c0001t0034g0001 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-159+1036delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41087141 | |||||
| chrX:41087357
|
CT | C | 1 | a0001c0001t0008g0103 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-159+1250delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41087357 | |||||
| chrX:41087378
|
C | CT | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-159+1269_-159+127 others(5): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41087378 | ||||||
| chrX:41087380
|
T | G | 64 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(61): Show | 64 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.-159+1271T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41087380 | ||||||
| chrX:41087492
|
A | G | 63 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(60): Show | 63 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.-159+1383A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41087492 | ||||||
| chrX:41087612
|
TC | T | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-159+1505delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41087612 | |||||
| chrX:41087752
|
C | G | 1 | a0001c0001t0001g0232 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-159+1643C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41087752 | ||||||
| chrX:41087907
|
T | C | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-159+1798T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41087907 | ||||||
| chrX:41087919
|
A | T | 61 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(58): Show | 61 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.-159+1810A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41087919 | ||||||
| chrX:41088008
|
G | GT | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-159+1906dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41088008 | |||||
| chrX:41088022
|
C | T | 5 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0101others(2): Show | 5 | NA18955.hp1 NA19000.hp1 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.-159+1913C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41088022 | ||||||
| chrX:41088052
|
CG | C | 1 | a0001c0001t0034g0001 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-159+1945delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41088052 | |||||
| chrX:41088074
|
C | A | 1 | a0001c0001t0027g0104 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-159+1965C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41088074 | ||||||
| chrX:41088113
|
A | G | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-159+2004A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41088113 | ||||||
| chrX:41088167
|
T | TAG | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-159+2062_-159+206 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41088167 | |||||
| chrX:41088206
|
A | ATC | 1 | a0001c0001t0001g0231 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-159+2100_-159+210 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41088206 | |||||
| chrX:41088215
|
C | T | 9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 9 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-159+2106C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41088215 | ||||||
| chrX:41088226
|
G | C | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-159+2117G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41088226 | ||||||
| chrX:41088227
|
C | G | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-159+2118C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41088227 | ||||||
| chrX:41088250
|
A | G | 1 | a0001c0001t0027g0104 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-159+2141A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41088250 | ||||||
| chrX:41088343
|
T | C | 134 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0109others(131): Show | 134 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.-159+2234T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41088343 | ||||||
| chrX:41088526
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-159+2417A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41088526 | ||||||
| chrX:41088691
|
G | T | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-159+2582G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41088691 | ||||||
| chrX:41088717
|
T | TA | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-159+2609dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41088717 | |||||
| chrX:41088765
|
CT | C | 2 | a0001c0001t0004g0237a0001c0001t0034g0001 | 2 | NA18941.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.-159+2666delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41088765 | |||||
| chrX:41088977
|
C | CA | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-159+2875dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41088977 | |||||
| chrX:41089001
|
AC | A | 1 | a0001c0001t0034g0001 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-159+2897delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41089001 | |||||
| chrX:41089077
|
T | G | 1 | a0001c0001t0002g0011 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-159+2968T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41089077 | ||||||
| chrX:41089160
|
A | AT | 1 | a0001c0001t0002g0097 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-159+3058dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41089160 | |||||
| chrX:41089208
|
AT | A | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-159+3101delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41089208 | |||||
| chrX:41089394
|
T | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(10): Show | 13 | HG00438.hp2 HG02074.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-159+3285T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41089394 | ||||||
| chrX:41089584
|
A | G | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG01167.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-159+3475A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41089584 | ||||||
| chrX:41089599
|
C | T | 3 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096 | 3 | HG02572.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-159+3490C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41089599 | ||||||
| chrX:41089652
|
TTC | T | 1 | a0001c0001t0004g0277 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-159+3545_-159+354 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41089652 | |||||
| chrX:41089691
|
C | T | 1 | a0001c0001t0003g0293 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-159+3582C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41089691 | ||||||
| chrX:41089773
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-159+3664C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41089773 | ||||||
| chrX:41089903
|
G | GT | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(10): Show | 13 | HG00673.hp1 HG02055.hp1 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.-159+3822dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41089903 | |||||
| chrX:41089903
|
G | GTTTTT | 2 | a0001c0001t0003g0238a0001c0001t0003g0239 | 2 | NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-159+3818_-159+382 others(9): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41089903 | |||||
| chrX:41089903
|
G | GTTTTTT | 19 | a0001c0001t0002g0106a0001c0001t0003g0241a0001c0001t0003g0243others(16): Show | 19 | HG00423.hp1 HG00597.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-159+3817_-159+382 others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41089903 | |||||
| chrX:41089903
|
G | GTTTTTTT | 27 | a0001c0001t0003g0254a0001c0001t0003g0259a0001c0001t0003g0261others(24): Show | 27 | HG00323.hp1 HG01109.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.-159+3816_-159+382 others(11): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41089903 | |||||
| chrX:41089903
|
G | GTTTTTTT others(1): Show |
9 | a0001c0001t0002g0108a0001c0001t0003g0274a0001c0001t0003g0281others(6): Show | 9 | HG02004.hp1 HG02109.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-159+3815_-159+382 others(12): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41089903 | |||||
| chrX:41089903
|
G | GTTTTTTT others(2): Show |
1 | a0001c0001t0003g0276 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-159+3814_-159+382 others(13): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41089903 | |||||
| chrX:41089903
|
GT | G | 133 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(130): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-159+3822delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41089903 | |||||
| chrX:41089903
|
GTT | G | 21 | a0001c0001t0001g0115a0001c0001t0001g0124a0001c0001t0001g0125others(18): Show | 21 | HG00099.hp2 HG01070.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.-159+3821_-159+382 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41089903 | |||||
| chrX:41089903
|
GTTT | G | 2 | a0001c0001t0005g0012a0007c0012t0001g0105 | 2 | HG03453.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.-159+3820_-159+382 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41089903 | |||||
| chrX:41089903
|
GTTTT | G | 1 | a0001c0001t0003g0282 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-159+3819_-159+382 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41089903 | |||||
| chrX:41089931
|
T | C | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-159+3822T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41089931 | ||||||
| chrX:41090003
|
TCAGG | T | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+3895_-159+389 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41090003 | ||||||
| chrX:41090073
|
A | AT | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+3972dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41090073 | |||||
| chrX:41090082
|
C | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-159+3973C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41090082 | ||||||
| chrX:41090183
|
C | G | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-159+4074C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41090183 | ||||||
| chrX:41090184
|
G | C | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-159+4075G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41090184 | ||||||
| chrX:41090330
|
CACTT | C | 1 | a0001c0001t0001g0109 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-159+4224_-159+422 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41090330 | |||||
| chrX:41090557
|
CA | C | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+4450delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41090557 | |||||
| chrX:41090665
|
G | GT | 2 | a0001c0001t0005g0066a0008c0006t0001g0002 | 2 | HG02602.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.-159+4565dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41090665 | |||||
| chrX:41090679
|
T | TC | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+4573dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41090679 | |||||
| chrX:41090701
|
AT | A | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+4594delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41090701 | |||||
| chrX:41090725
|
G | GT | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+4618dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41090725 | |||||
| chrX:41090753
|
T | C | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-159+4644T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41090753 | ||||||
| chrX:41090891
|
C | T | 1 | a0001c0001t0034g0001 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-159+4782C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41090891 | ||||||
| chrX:41091040
|
T | C | 1 | a0001c0001t0005g0067 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-159+4931T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41091040 | ||||||
| chrX:41091060
|
CAT | C | 1 | a0001c0001t0001g0192 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-159+4954_-159+495 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41091060 | |||||
| chrX:41091186
|
T | TA | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+5078dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41091186 | |||||
| chrX:41091212
|
A | ACT | 197 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.-159+5104_-159+510 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41091212 | |||||
| chrX:41091240
|
G | GT | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+5135dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41091240 | |||||
| chrX:41091368
|
GT | G | 1 | a0001c0001t0001g0006 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-159+5260delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41091368 | ||||||
| chrX:41091591
|
G | GT | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+5485dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41091591 | |||||
| chrX:41092173
|
C | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-159+6064C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41092173 | ||||||
| chrX:41092182
|
T | A | 1 | a0001c0001t0001g0214 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-159+6073T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41092182 | ||||||
| chrX:41092540
|
A | G | 1 | a0001c0001t0002g0065 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-159+6431A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41092540 | ||||||
| chrX:41092680
|
G | GA | 1 | a0001c0001t0002g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-159+6576dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41092680 | |||||
| chrX:41092682
|
AAAAC | A | 31 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.-159+6576_-159+657 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41092682 | |||||
| chrX:41092692
|
G | GGT | 1 | a0001c0001t0005g0066 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-159+6595_-159+659 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41092692 | |||||
| chrX:41092863
|
C | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-159+6754C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41092863 | ||||||
| chrX:41092879
|
A | AT | 2 | a0001c0001t0001g0212a0001c0001t0002g0102 | 2 | NA19000.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-159+6781dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41092879 | |||||
| chrX:41092933
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-159+6824C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41092933 | ||||||
| chrX:41093247
|
T | G | 1 | a0001c0001t0002g0068 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-159+7138T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41093247 | ||||||
| chrX:41093376
|
G | C | 1 | a0001c0001t0001g0129 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-159+7267G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41093376 | ||||||
| chrX:41093398
|
TA | T | 1 | a0001c0001t0002g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-159+7292delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41093398 | |||||
| chrX:41093475
|
G | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-159+7366G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41093475 | ||||||
| chrX:41093767
|
A | G | 2 | a0001c0001t0013g0180a0001c0001t0028g0179 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-159+7658A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41093767 | ||||||
| chrX:41094184
|
C | CTTTTT | 59 | a0001c0001t0001g0131a0001c0001t0001g0194a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-159+8080_-159+808 others(9): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41094184 | |||||
| chrX:41094184
|
C | CTTTTTT | 138 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.-159+8079_-159+808 others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41094184 | |||||
| chrX:41094221
|
G | T | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-159+8112G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41094221 | ||||||
| chrX:41094231
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0213 | 2 | HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-159+8122C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41094231 | ||||||
| chrX:41094337
|
C | T | 3 | a0001c0001t0005g0012a0001c0001t0005g0063a0001c0001t0005g0064 | 3 | NA18939.hp2 NA18960.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.-159+8228C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41094337 | ||||||
| chrX:41094465
|
C | T | 3 | a0001c0001t0005g0090a0001c0001t0005g0091a0001c0001t0005g0092 | 3 | HG02148.hp1 NA18973.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-159+8356C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41094465 | ||||||
| chrX:41094503
|
C | T | 1 | a0001c0001t0024g0234 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-159+8394C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41094503 | ||||||
| chrX:41094645
|
T | TCCATA | 8 | a0001c0002t0002g0118a0001c0002t0002g0119a0001c0002t0002g0120others(5): Show | 8 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-159+8537_-159+854 others(9): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41094645 | |||||
| chrX:41094676
|
AT | A | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+8571delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41094676 | |||||
| chrX:41094724
|
C | G | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-159+8615C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41094724 | ||||||
| chrX:41094725
|
G | A | 2 | a0001c0001t0013g0180a0001c0001t0028g0179 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-159+8616G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41094725 | ||||||
| chrX:41094781
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-159+8672G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41094781 | ||||||
| chrX:41094836
|
C | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-159+8727C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41094836 | ||||||
| chrX:41094863
|
A | AC | 1 | a0001c0001t0002g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-159+8759dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41094863 | |||||
| chrX:41094953
|
TC | T | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+8847delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41094953 | |||||
| chrX:41095008
|
C | G | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-159+8899C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41095008 | ||||||
| chrX:41095043
|
C | CA | 8 | a0001c0001t0001g0227a0001c0001t0004g0237a0001c0001t0007g0017others(5): Show | 8 | HG00280.hp1 HG03209.hp1 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.-159+8950dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41095043 | |||||
| chrX:41095043
|
CA | C | 58 | a0001c0001t0001g0230a0001c0001t0002g0062a0001c0001t0003g0238others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.-159+8950delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41095043 | |||||
| chrX:41095043
|
CAAAAA | C | 2 | a0001c0001t0013g0180a0001c0001t0028g0179 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-159+8946_-159+895 others(9): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41095043 | |||||
| chrX:41095564
|
A | G | 1 | a0001c0001t0004g0272 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-159+9455A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41095564 | ||||||
| chrX:41095729
|
A | C | 1 | a0001c0002t0002g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-159+9620A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41095729 | ||||||
| chrX:41095749
|
T | C | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-159+9640T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41095749 | ||||||
| chrX:41095780
|
G | C | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-159+9671G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41095780 | ||||||
| chrX:41095882
|
A | AT | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-159+9774dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41095882 | |||||
| chrX:41096039
|
T | A | 1 | a0001c0001t0005g0012 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-159+9930T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41096039 | ||||||
| chrX:41096189
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-159+10080C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41096189 | ||||||
| chrX:41096194
|
T | TC | 2 | a0001c0001t0002g0210a0006c0007t0020g0098 | 2 | HG02615.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.-159+10092dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41096194 | |||||
| chrX:41096445
|
AT | A | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+10340delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41096445 | |||||
| chrX:41096600
|
C | T | 73 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0131others(70): Show | 73 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.-159+10491C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41096600 | ||||||
| chrX:41096604
|
G | T | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.-159+10495G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41096604 | ||||||
| chrX:41097023
|
T | G | 1 | a0001c0001t0001g0110 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-159+10914T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41097023 | ||||||
| chrX:41097041
|
C | CTG | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-159+10937_-159+10 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41097041 | |||||
| chrX:41097569
|
T | C | 1 | a0001c0001t0019g0018 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-159+11460T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41097569 | ||||||
| chrX:41097667
|
T | C | 1 | a0001c0001t0003g0276 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-159+11558T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41097667 | ||||||
| chrX:41097683
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-159+11574C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41097683 | ||||||
| chrX:41097769
|
TG | T | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-159+11662delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41097769 | |||||
| chrX:41097786
|
A | G | 1 | a0001c0001t0003g0289 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-159+11677A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41097786 | ||||||
| chrX:41097813
|
TG | T | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+11706delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41097813 | |||||
| chrX:41097978
|
C | A | 2 | a0001c0001t0003g0284a0001c0001t0003g0290 | 2 | HG03669.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-159+11869C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41097978 | ||||||
| chrX:41098032
|
A | AT | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+11924dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41098032 | |||||
| chrX:41098053
|
G | C | 1 | a0001c0002t0002g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-159+11944G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41098053 | ||||||
| chrX:41098139
|
C | CT | 1 | a0001c0001t0002g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-159+12046dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41098139 | |||||
| chrX:41098139
|
CT | C | 6 | a0001c0001t0001g0134a0001c0001t0001g0191a0001c0001t0001g0198others(3): Show | 6 | HG02615.hp1 HG02896.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.-159+12046delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41098139 | |||||
| chrX:41098233
|
TG | T | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+12127delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41098233 | |||||
| chrX:41098263
|
C | A | 1 | a0001c0001t0001g0199 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-159+12154C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41098263 | ||||||
| chrX:41098307
|
ATT | A | 1 | a0001c0001t0002g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-159+12201_-159+12 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41098307 | |||||
| chrX:41098351
|
G | GC | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+12243dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41098351 | |||||
| chrX:41098432
|
G | GC | 1 | a0001c0001t0003g0271 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-159+12326dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41098432 | |||||
| chrX:41098503
|
C | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(2): Show | 5 | HG02165.hp1 NA18981.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.-159+12394C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41098503 | ||||||
| chrX:41098503
|
CTA | C | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+12399_-159+12 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41098503 | |||||
| chrX:41098561
|
CT | C | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-159+12455delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41098561 | |||||
| chrX:41098568
|
G | GT | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+12466dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41098568 | |||||
| chrX:41098674
|
G | GC | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+12567dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41098674 | |||||
| chrX:41098785
|
A | C | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-159+12676A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41098785 | ||||||
| chrX:41098806
|
AAGTGCTG others(392): Show |
A | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-159+12725_-159+13 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41098806 | |||||
| chrX:41098835
|
G | A | 1 | a0001c0001t0003g0285 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-159+12726G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41098835 | ||||||
| chrX:41098850
|
C | T | 1 | a0001c0001t0005g0092 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-159+12741C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41098850 | ||||||
| chrX:41098876
|
G | A | 4 | a0001c0002t0002g0196a0001c0002t0002g0215a0001c0002t0021g0195others(1): Show | 4 | HG03486.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-159+12767G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41098876 | ||||||
| chrX:41098902
|
A | AG | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+12793_-159+12 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41098902 | ||||||
| chrX:41098922
|
G | GT | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-159+12820dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41098922 | |||||
| chrX:41099059
|
TG | T | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+12953delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099059 | |||||
| chrX:41099082
|
A | G | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-159+12973A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41099082 | ||||||
| chrX:41099096
|
G | GT | 54 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0134others(51): Show | 54 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.-159+13013dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
G | GTT | 26 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0158others(23): Show | 26 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.-159+13012_-159+13 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
G | GTTT | 15 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0207others(12): Show | 15 | HG01891.hp2 HG01978.hp2 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.-159+13011_-159+13 others(9): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
G | GTTTT | 3 | a0001c0002t0002g0196a0001c0002t0002g0215a0001c0008t0002g0216 | 3 | HG03486.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-159+13010_-159+13 others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
G | GTTTTTTT | 1 | a0001c0002t0002g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-159+13007_-159+13 others(13): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
G | GTTTTTTT others(2): Show |
5 | a0001c0001t0003g0241a0001c0001t0003g0243a0001c0001t0003g0254others(2): Show | 5 | HG01074.hp1 HG01243.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-159+13005_-159+13 others(15): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
G | GTTTTTTT others(3): Show |
22 | a0001c0001t0002g0106a0001c0001t0003g0239a0001c0001t0003g0244others(19): Show | 22 | HG00597.hp2 HG01109.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.-159+13004_-159+13 others(16): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
G | GTTTTTTT others(4): Show |
16 | a0001c0001t0002g0108a0001c0001t0003g0261a0001c0001t0003g0263others(13): Show | 16 | HG00323.hp1 HG01175.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.-159+13003_-159+13 others(17): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
G | GTTTTTTT others(5): Show |
9 | a0001c0001t0003g0269a0001c0001t0003g0271a0001c0001t0003g0281others(6): Show | 9 | HG00423.hp1 HG01978.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.-159+13002_-159+13 others(18): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
G | GTTTTTTT others(6): Show |
2 | a0001c0001t0003g0253a0001c0001t0030g0275 | 2 | HG02109.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-159+13001_-159+13 others(19): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
G | GTTTTTTT others(7): Show |
1 | a0001c0001t0004g0277 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-159+13000_-159+13 others(20): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
G | GTTTTTTT others(12): Show |
1 | a0001c0004t0002g0177 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-159+12995_-159+13 others(25): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
G | GTTTTTTT others(13): Show |
2 | a0001c0001t0003g0292a0001c0004t0002g0178 | 2 | HG02723.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-159+12994_-159+13 others(26): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
G | GTTTTTTT others(28): Show |
1 | a0001c0004t0002g0211 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-159+13013_-159+13 others(41): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
GT | G | 8 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0019others(5): Show | 8 | HG00323.hp2 HG01168.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-159+13013delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
GTT | G | 1 | a0001c0001t0013g0180 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-159+13012_-159+13 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
GTTT | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(1): Show | 4 | HG03195.hp1 NA18951.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-159+13011_-159+13 others(9): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
GTTTT | G | 28 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(25): Show | 28 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.-159+13010_-159+13 others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
GTTTTTT | G | 8 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-159+13008_-159+13 others(12): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
GTTTTTTT | G | 1 | a0001c0001t0032g0222 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-159+13007_-159+13 others(13): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099096
|
GTTTTTTT others(1): Show |
G | 3 | a0001c0001t0008g0135a0001c0001t0008g0136a0001c0001t0008g0137 | 3 | HG01168.hp2 HG01192.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.-159+13006_-159+13 others(14): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099096 | |||||
| chrX:41099099
|
T | TTTTTTTT others(6): Show |
2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-159+13002_-159+13 others(19): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099099 | |||||
| chrX:41099102
|
T | TTTTTTTT others(2): Show |
1 | a0001c0001t0003g0238 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-159+13001_-159+13 others(15): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099102 | |||||
| chrX:41099116
|
TTTTTTTA | T | 1 | a0001c0001t0003g0286 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-159+13008_-159+13 others(13): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41099116 | ||||||
| chrX:41099119
|
TTTTA | T | 1 | a0001c0001t0003g0276 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-159+13011_-159+13 others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41099119 | ||||||
| chrX:41099123
|
A | T | 57 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(54): Show | 57 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.-159+13014A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41099123 | ||||||
| chrX:41099246
|
C | T | 1 | a0001c0001t0002g0056 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-159+13137C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41099246 | ||||||
| chrX:41099386
|
C | T | 31 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.-159+13277C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41099386 | ||||||
| chrX:41099414
|
G | GTC | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+13306_-159+13 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099414 | |||||
| chrX:41099696
|
CT | C | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+13591delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099696 | |||||
| chrX:41099705
|
ATAAACT | A | 2 | a0001c0001t0002g0062a0001c0001t0002g0083 | 2 | HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-159+13600_-159+13 others(12): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099705 | |||||
| chrX:41099706
|
TA | T | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+13600delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099706 | |||||
| chrX:41099744
|
A | G | 1 | a0001c0001t0012g0082 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-159+13635A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41099744 | ||||||
| chrX:41099795
|
G | A | 2 | a0001c0001t0002g0013a0001c0001t0022g0014 | 2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-159+13686G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41099795 | ||||||
| chrX:41099811
|
A | G | 2 | a0001c0001t0010g0156a0001c0001t0010g0157 | 2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.-159+13702A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41099811 | ||||||
| chrX:41099905
|
T | TA | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-159+13797dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41099905 | |||||
| chrX:41099916
|
C | G | 1 | a0001c0001t0002g0081 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-159+13807C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41099916 | ||||||
| chrX:41100630
|
CTTAT | C | 1 | a0001c0001t0002g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-159+14524_-159+14 others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41100630 | |||||
| chrX:41101088
|
T | C | 1 | a0001c0001t0004g0255 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-159+14979T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41101088 | ||||||
| chrX:41101187
|
C | T | 2 | a0001c0002t0002g0121a0001c0002t0002g0122 | 2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-159+15078C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41101187 | ||||||
| chrX:41101214
|
T | C | 9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 9 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-159+15105T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41101214 | ||||||
| chrX:41101229
|
C | A | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-159+15120C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41101229 | ||||||
| chrX:41101309
|
GT | G | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-159+15201delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41101309 | ||||||
| chrX:41101346
|
T | G | 1 | a0001c0001t0027g0104 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-159+15237T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41101346 | ||||||
| chrX:41101423
|
C | CA | 5 | a0001c0001t0001g0140a0001c0001t0002g0084a0001c0001t0002g0108others(2): Show | 5 | HG02738.hp1 NA18989.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.-159+15328dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41101423 | |||||
| chrX:41101423
|
CA | C | 10 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(7): Show | 10 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-159+15328delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41101423 | |||||
| chrX:41101449
|
T | C | 1 | a0001c0001t0023g0022 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-159+15340T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41101449 | ||||||
| chrX:41101595
|
C | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-159+15486C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41101595 | ||||||
| chrX:41101614
|
A | G | 2 | a0001c0001t0004g0260a0001c0001t0004g0268 | 2 | NA19009.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-159+15505A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41101614 | ||||||
| chrX:41101656
|
A | G | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.-159+15547A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41101656 | ||||||
| chrX:41101682
|
T | TA | 4 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(1): Show | 4 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.-159+15581dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41101682 | |||||
| chrX:41101691
|
T | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(27): Show | 30 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.-159+15582T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41101691 | ||||||
| chrX:41101695
|
T | A | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(2): Show | 5 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.-159+15586T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41101695 | ||||||
| chrX:41101719
|
T | A | 1 | a0001c0001t0001g0141 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-159+15610T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41101719 | ||||||
| chrX:41101869
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0200 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-159+15760G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41101869 | ||||||
| chrX:41101876
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-159+15767C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41101876 | ||||||
| chrX:41101931
|
C | A | 1 | a0001c0001t0001g0207 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-159+15822C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41101931 | ||||||
| chrX:41102049
|
G | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-159+15940G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41102049 | ||||||
| chrX:41102074
|
A | G | 4 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(1): Show | 4 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.-159+15965A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41102074 | ||||||
| chrX:41102234
|
G | T | 1 | a0001c0001t0004g0278 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-159+16125G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41102234 | ||||||
| chrX:41102310
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-159+16201G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41102310 | ||||||
| chrX:41102333
|
C | T | 74 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0131others(71): Show | 74 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.-159+16224C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41102333 | ||||||
| chrX:41102497
|
C | G | 2 | a0001c0001t0001g0140a0001c0001t0001g0212 | 2 | NA18992.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-159+16388C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41102497 | ||||||
| chrX:41102697
|
G | T | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-159+16588G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41102697 | ||||||
| chrX:41102798
|
C | CT | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(134): Show | 137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.-159+16701dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41102798 | |||||
| chrX:41102841
|
G | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-159+16732G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41102841 | ||||||
| chrX:41102873
|
A | C | 1 | a0001c0001t0003g0290 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-159+16764A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41102873 | ||||||
| chrX:41103201
|
A | G | 1 | a0001c0001t0002g0055 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-159+17092A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41103201 | ||||||
| chrX:41103212
|
A | G | 8 | a0001c0002t0002g0118a0001c0002t0002g0119a0001c0002t0002g0120others(5): Show | 8 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-159+17103A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41103212 | ||||||
| chrX:41103403
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-159+17294G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41103403 | ||||||
| chrX:41103452
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-159+17343C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41103452 | ||||||
| chrX:41103520
|
A | G | 2 | a0001c0001t0002g0193a0001c0002t0002g0174 | 2 | HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-159+17411A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41103520 | ||||||
| chrX:41103662
|
C | T | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-159+17553C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41103662 | ||||||
| chrX:41103699
|
A | C | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-159+17590A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41103699 | ||||||
| chrX:41103788
|
T | C | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-159+17679T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41103788 | ||||||
| chrX:41103860
|
AT | A | 1 | a0001c0001t0003g0271 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-159+17754delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41103860 | |||||
| chrX:41103893
|
A | AG | 1 | a0001c0001t0003g0271 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-159+17787dupG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41103893 | |||||
| chrX:41104179
|
G | A | 1 | a0001c0001t0024g0234 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-159+18070G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41104179 | ||||||
| chrX:41104204
|
C | G | 1 | a0001c0001t0012g0082 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-159+18095C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41104204 | ||||||
| chrX:41104219
|
A | AC | 1 | a0006c0007t0020g0098 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-159+18112dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41104219 | |||||
| chrX:41104538
|
C | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-159+18429C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41104538 | ||||||
| chrX:41104575
|
C | A | 2 | a0001c0001t0008g0103a0001c0001t0008g0142 | 2 | HG01070.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-159+18466C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41104575 | ||||||
| chrX:41104622
|
C | CA | 1 | a0001c0001t0003g0271 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-159+18518dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41104622 | |||||
| chrX:41104770
|
A | C | 1 | a0001c0001t0001g0155 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-159+18661A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41104770 | ||||||
| chrX:41104802
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-158-18669A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41104802 | ||||||
| chrX:41104874
|
C | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-158-18597C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41104874 | ||||||
| chrX:41104898
|
C | G | 34 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0134others(31): Show | 34 | HG00738.hp1 HG00741.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-158-18573C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41104898 | ||||||
| chrX:41105202
|
T | G | 1 | a0001c0001t0002g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-158-18269T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41105202 | ||||||
| chrX:41105237
|
T | TG | 1 | a0001c0001t0005g0063 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-158-18232dupG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41105237 | |||||
| chrX:41105420
|
C | A | 1 | a0001c0001t0001g0214 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-158-18051C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41105420 | ||||||
| chrX:41105553
|
C | T | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(132): Show | 135 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.-158-17918C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41105553 | ||||||
| chrX:41106172
|
CTTTTGGT others(22): Show |
C | 1 | a0001c0001t0002g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-158-17298_-158-17 others(35): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41106172 | ||||||
| chrX:41106202
|
G | A | 1 | a0001c0001t0002g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-158-17269G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41106202 | ||||||
| chrX:41106203
|
C | A | 1 | a0001c0001t0002g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-158-17268C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41106203 | ||||||
| chrX:41106257
|
G | GT | 2 | a0001c0001t0001g0214a0001c0001t0008g0137 | 2 | HG03490.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-158-17207dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41106257 | |||||
| chrX:41106361
|
T | G | 6 | a0001c0002t0002g0118a0001c0002t0002g0119a0001c0002t0002g0120others(3): Show | 6 | HG02258.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-158-17110T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41106361 | ||||||
| chrX:41106435
|
A | G | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-158-17036A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41106435 | ||||||
| chrX:41106451
|
G | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-158-17020G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41106451 | ||||||
| chrX:41106522
|
A | AT | 51 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0155others(48): Show | 51 | HG00621.hp1 HG00735.hp2 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.-158-16922dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41106522 | |||||
| chrX:41106522
|
A | ATT | 51 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0002g0106others(48): Show | 51 | HG00323.hp1 HG00597.hp2 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.-158-16923_-158-16 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41106522 | |||||
| chrX:41106522
|
A | ATTT | 18 | a0001c0001t0002g0108a0001c0001t0003g0243a0001c0001t0003g0259others(15): Show | 18 | HG00423.hp1 HG01175.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.-158-16924_-158-16 others(9): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41106522 | |||||
| chrX:41106522
|
AT | A | 31 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.-158-16922delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41106522 | |||||
| chrX:41106522
|
ATTT | A | 1 | a0001c0001t0024g0234 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-158-16924_-158-16 others(9): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41106522 | |||||
| chrX:41106857
|
G | T | 8 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(5): Show | 8 | HG00099.hp2 HG00733.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.-158-16614G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41106857 | ||||||
| chrX:41106865
|
TTTTC | T | 1 | a0001c0001t0001g0214 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-158-16594_-158-16 others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41106865 | |||||
| chrX:41106887
|
C | CT | 16 | a0001c0001t0001g0154a0001c0001t0001g0167a0001c0001t0001g0168others(13): Show | 16 | HG00408.hp2 HG00423.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.-158-16567dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41106887 | |||||
| chrX:41106887
|
CT | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0110a0001c0001t0001g0131others(4): Show | 7 | HG01943.hp1 HG02895.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-158-16567delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41106887 | |||||
| chrX:41106887
|
CTTTTT | C | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-158-16571_-158-16 others(11): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41106887 | |||||
| chrX:41107234
|
G | T | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-158-16237G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41107234 | ||||||
| chrX:41107262
|
A | C | 1 | a0001c0001t0001g0230 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-158-16209A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41107262 | ||||||
| chrX:41107431
|
G | GT | 1 | a0001c0001t0001g0182 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-158-16039dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41107431 | |||||
| chrX:41107443
|
C | G | 31 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.-158-16028C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41107443 | ||||||
| chrX:41107550
|
C | T | 1 | a0001c0001t0003g0288 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-158-15921C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41107550 | ||||||
| chrX:41107772
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-158-15699C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41107772 | ||||||
| chrX:41107797
|
G | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-158-15674G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41107797 | ||||||
| chrX:41107907
|
A | G | 5 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0101others(2): Show | 5 | NA18955.hp1 NA19000.hp1 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.-158-15564A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41107907 | ||||||
| chrX:41107911
|
T | C | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.-158-15560T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41107911 | ||||||
| chrX:41107927
|
G | A | 1 | a0001c0001t0003g0261 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-158-15544G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41107927 | ||||||
| chrX:41107972
|
A | T | 1 | a0001c0001t0002g0048 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-158-15499A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41107972 | ||||||
| chrX:41108026
|
A | T | 1 | a0001c0001t0001g0155 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-158-15445A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41108026 | ||||||
| chrX:41108136
|
A | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-158-15335A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41108136 | ||||||
| chrX:41108299
|
A | G | 1 | a0001c0002t0002g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-158-15172A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41108299 | ||||||
| chrX:41108340
|
C | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-158-15131C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41108340 | ||||||
| chrX:41108492
|
A | C | 14 | a0001c0001t0002g0193a0001c0002t0002g0118a0001c0002t0002g0119others(11): Show | 14 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-158-14979A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41108492 | ||||||
| chrX:41108908
|
A | T | 1 | a0001c0002t0002g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-158-14563A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41108908 | ||||||
| chrX:41109135
|
TTAAA | T | 1 | a0001c0001t0027g0104 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-158-14330_-158-14 others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41109135 | |||||
| chrX:41109273
|
G | T | 292 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.-158-14198G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41109273 | ||||||
| chrX:41109368
|
T | C | 3 | a0001c0001t0002g0013a0001c0001t0022g0014a0001c0001t0027g0104 | 3 | HG02922.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-158-14103T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41109368 | ||||||
| chrX:41109577
|
TA | T | 3 | a0001c0001t0003g0259a0001c0001t0003g0274a0001c0001t0031g0273 | 3 | HG02523.hp1 NA19063.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-158-13892delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41109577 | |||||
| chrX:41109635
|
T | A | 1 | a0001c0001t0002g0069 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-158-13836T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41109635 | ||||||
| chrX:41109763
|
CTG | C | 31 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.-158-13707_-158-13 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41109763 | ||||||
| chrX:41109770
|
T | TG | 52 | a0001c0001t0001g0197a0001c0001t0001g0218a0001c0001t0001g0219others(49): Show | 52 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.-158-13693dupG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41109770 | |||||
| chrX:41109770
|
T | TGG | 7 | a0001c0001t0003g0250a0001c0001t0003g0261a0001c0001t0003g0263others(4): Show | 7 | HG01109.hp1 NA18747.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.-158-13694_-158-13 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41109770 | |||||
| chrX:41109770
|
TG | T | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-158-13693delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41109770 | |||||
| chrX:41109779
|
C | T | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-158-13692C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41109779 | ||||||
| chrX:41110083
|
G | C | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-158-13388G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41110083 | ||||||
| chrX:41110143
|
G | A | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-158-13328G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41110143 | ||||||
| chrX:41110240
|
A | C | 1 | a0001c0001t0001g0153 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-158-13231A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41110240 | ||||||
| chrX:41110420
|
G | A | 3 | a0001c0001t0009g0025a0001c0001t0009g0061a0001c0001t0009g0233 | 3 | HG00099.hp1 HG00735.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.-158-13051G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41110420 | ||||||
| chrX:41110442
|
G | GT | 1 | a0001c0001t0002g0089 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-158-13026dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41110442 | |||||
| chrX:41110541
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-158-12930A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41110541 | ||||||
| chrX:41110672
|
C | T | 2 | a0001c0001t0010g0156a0001c0001t0010g0157 | 2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.-158-12799C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41110672 | ||||||
| chrX:41111017
|
G | C | 1 | a0001c0008t0002g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-158-12454G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41111017 | ||||||
| chrX:41111111
|
G | T | 1 | a0001c0001t0001g0152 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-158-12360G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41111111 | ||||||
| chrX:41111146
|
T | TGGTATTA others(1): Show |
59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-158-12324_-158-12 others(14): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41111146 | |||||
| chrX:41111244
|
C | G | 3 | a0001c0001t0002g0069a0001c0001t0002g0085a0001c0001t0002g0097 | 3 | NA18970.hp1 NA18979.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.-158-12227C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41111244 | ||||||
| chrX:41111302
|
C | T | 2 | a0001c0001t0002g0078a0001c0001t0002g0088 | 2 | NA18951.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-158-12169C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41111302 | ||||||
| chrX:41111461
|
A | AT | 1 | a0001c0001t0003g0283 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-158-12008dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41111461 | |||||
| chrX:41111844
|
A | AT | 3 | a0001c0001t0002g0047a0001c0001t0002g0065a0001c0001t0005g0091 | 3 | HG02148.hp1 HG04228.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.-158-11609dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41111844 | |||||
| chrX:41111844
|
AT | A | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(180): Show | 183 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.-158-11609delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41111844 | |||||
| chrX:41111844
|
ATT | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0198a0001c0001t0001g0201others(1): Show | 4 | HG01167.hp1 HG01975.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.-158-11610_-158-11 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41111844 | |||||
| chrX:41112007
|
G | A | 14 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(11): Show | 14 | HG00323.hp1 HG02004.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-158-11464G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41112007 | ||||||
| chrX:41112172
|
G | A | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.-158-11299G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41112172 | ||||||
| chrX:41112177
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-158-11294A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41112177 | ||||||
| chrX:41112576
|
GAAT | G | 1 | a0001c0001t0001g0220 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-158-10890_-158-10 others(9): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41112576 | |||||
| chrX:41112598
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-158-10873T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41112598 | ||||||
| chrX:41112653
|
G | GA | 1 | a0001c0001t0001g0006 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-158-10810dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41112653 | |||||
| chrX:41113043
|
C | T | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-158-10428C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41113043 | ||||||
| chrX:41113195
|
C | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-158-10276C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41113195 | ||||||
| chrX:41113491
|
G | A | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-158-9980G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41113491 | ||||||
| chrX:41113632
|
A | G | 1 | a0001c0001t0004g0266 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-158-9839A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41113632 | ||||||
| chrX:41113785
|
TAAGA | T | 2 | a0001c0002t0002g0121a0001c0002t0002g0122 | 2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-158-9682_-158-967 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41113785 | |||||
| chrX:41113985
|
A | C | 1 | a0001c0001t0001g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-158-9486A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41113985 | ||||||
| chrX:41113993
|
C | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-158-9478C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41113993 | ||||||
| chrX:41114224
|
T | C | 285 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-158-9247T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41114224 | ||||||
| chrX:41114225
|
C | T | 9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 9 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-158-9246C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41114225 | ||||||
| chrX:41114486
|
C | CT | 20 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0101others(17): Show | 20 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.-158-8971dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41114486 | |||||
| chrX:41114486
|
CT | C | 5 | a0001c0001t0001g0146a0001c0001t0001g0153a0001c0001t0001g0230others(2): Show | 5 | HG01167.hp1 HG02895.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.-158-8971delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41114486 | |||||
| chrX:41114680
|
T | C | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-158-8791T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41114680 | ||||||
| chrX:41114816
|
G | T | 9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 9 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-158-8655G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41114816 | ||||||
| chrX:41115221
|
C | CA | 3 | a0001c0001t0001g0204a0001c0001t0001g0220a0006c0007t0020g0098 | 3 | HG01081.hp1 HG02135.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-158-8236dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41115221 | |||||
| chrX:41115221
|
CA | C | 1 | a0001c0001t0003g0276 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-158-8236delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41115221 | |||||
| chrX:41115222
|
AAAAAAAA others(13): Show |
A | 7 | a0001c0001t0002g0024a0001c0001t0002g0041a0001c0001t0002g0042others(4): Show | 7 | HG00642.hp1 HG01081.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.-158-8234_-158-821 others(24): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41115222 | |||||
| chrX:41115236
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-158-8235G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41115236 | ||||||
| chrX:41115238
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-158-8233A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41115238 | ||||||
| chrX:41115242
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-158-8229G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41115242 | ||||||
| chrX:41115242
|
G | GA | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(2): Show | 5 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.-158-8216dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41115242 | |||||
| chrX:41115242
|
GA | G | 78 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0131others(75): Show | 78 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-158-8216delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41115242 | |||||
| chrX:41115244
|
A | AAAAG | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-158-8224_-158-822 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41115244 | |||||
| chrX:41115244
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-158-8227A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41115244 | ||||||
| chrX:41115303
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-158-8168T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41115303 | ||||||
| chrX:41115325
|
T | C | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-158-8146T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41115325 | ||||||
| chrX:41115428
|
C | T | 31 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.-158-8043C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41115428 | ||||||
| chrX:41115447
|
A | C | 1 | a0001c0001t0002g0048 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-158-8024A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41115447 | ||||||
| chrX:41115632
|
A | G | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-158-7839A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41115632 | ||||||
| chrX:41115887
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-158-7584T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41115887 | ||||||
| chrX:41115967
|
G | C | 2 | a0001c0001t0003g0284a0001c0001t0003g0290 | 2 | HG03669.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-158-7504G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41115967 | ||||||
| chrX:41116208
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-158-7263G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41116208 | ||||||
| chrX:41116246
|
T | G | 1 | a0001c0001t0002g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-158-7225T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41116246 | ||||||
| chrX:41116534
|
T | C | 7 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0159others(4): Show | 7 | HG01081.hp1 HG01943.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.-158-6937T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41116534 | ||||||
| chrX:41116624
|
A | T | 2 | a0001c0001t0002g0062a0001c0001t0002g0083 | 2 | HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-158-6847A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41116624 | ||||||
| chrX:41116709
|
AT | A | 1 | a0001c0001t0005g0026 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-158-6755delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41116709 | |||||
| chrX:41116762
|
A | G | 1 | a0001c0001t0007g0020 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-158-6709A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41116762 | ||||||
| chrX:41116777
|
C | CT | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-158-6686dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41116777 | |||||
| chrX:41117326
|
G | A | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-158-6145G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41117326 | ||||||
| chrX:41117562
|
CT | C | 1 | a0001c0001t0008g0135 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-158-5899delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41117562 | |||||
| chrX:41117570
|
TTTC | T | 54 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(51): Show | 54 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.-158-5892_-158-589 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41117570 | |||||
| chrX:41117576
|
CTTCT | C | 1 | a0001c0001t0003g0261 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-158-5892_-158-588 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41117576 | |||||
| chrX:41117576
|
CTTCTTTT others(7): Show |
C | 1 | a0001c0001t0031g0273 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-158-5892_-158-587 others(18): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41117576 | |||||
| chrX:41117579
|
C | CT | 18 | a0001c0001t0001g0188a0001c0001t0001g0229a0001c0001t0001g0230others(15): Show | 18 | HG00738.hp1 HG01167.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-158-5876dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41117579 | |||||
| chrX:41117579
|
C | CTT | 1 | a0001c0002t0021g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-158-5877_-158-587 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41117579 | |||||
| chrX:41117579
|
CT | C | 5 | a0001c0001t0001g0147a0001c0001t0001g0160a0001c0001t0001g0161others(2): Show | 5 | HG02004.hp2 NA18939.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.-158-5876delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41117579 | |||||
| chrX:41117601
|
G | A | 4 | a0001c0002t0002g0196a0001c0002t0002g0215a0001c0002t0021g0195others(1): Show | 4 | HG03486.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-158-5870G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41117601 | ||||||
| chrX:41117653
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-158-5818C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41117653 | ||||||
| chrX:41117804
|
A | C | 197 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.-158-5667A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41117804 | ||||||
| chrX:41118087
|
T | C | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-158-5384T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41118087 | ||||||
| chrX:41118305
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0200 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-158-5166C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41118305 | ||||||
| chrX:41118306
|
T | G | 4 | a0001c0002t0002g0196a0001c0002t0002g0215a0001c0002t0021g0195others(1): Show | 4 | HG03486.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-158-5165T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41118306 | ||||||
| chrX:41118366
|
T | G | 193 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.-158-5105T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41118366 | ||||||
| chrX:41118466
|
CT | C | 2 | a0001c0001t0001g0131a0001c0001t0003g0259 | 2 | HG01943.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-158-5000delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41118466 | |||||
| chrX:41118524
|
GT | G | 1 | a0001c0001t0003g0274 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-158-4946delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41118524 | ||||||
| chrX:41118525
|
T | G | 55 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(52): Show | 55 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.-158-4946T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41118525 | ||||||
| chrX:41118685
|
G | A | 3 | a0001c0001t0009g0025a0001c0001t0009g0061a0001c0001t0009g0233 | 3 | HG00099.hp1 HG00735.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.-158-4786G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41118685 | ||||||
| chrX:41118829
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-158-4642G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41118829 | ||||||
| chrX:41118890
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(2): Show | 5 | HG02165.hp1 NA18981.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.-158-4581C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41118890 | ||||||
| chrX:41118948
|
A | G | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-158-4523A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41118948 | ||||||
| chrX:41119055
|
C | T | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.-158-4416C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41119055 | ||||||
| chrX:41119496
|
G | A | 1 | a0001c0002t0002g0215 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-158-3975G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41119496 | ||||||
| chrX:41119594
|
G | A | 1 | a0001c0001t0002g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-158-3877G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41119594 | ||||||
| chrX:41119599
|
TG | T | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-158-3870delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41119599 | |||||
| chrX:41119722
|
C | T | 31 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.-158-3749C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41119722 | ||||||
| chrX:41119850
|
A | AC | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-158-3620dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41119850 | |||||
| chrX:41119931
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-158-3540G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41119931 | ||||||
| chrX:41120008
|
A | AT | 57 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(54): Show | 57 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.-158-3453dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41120008 | |||||
| chrX:41120008
|
AT | A | 73 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0131others(70): Show | 73 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.-158-3453delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41120008 | |||||
| chrX:41120008
|
ATT | A | 1 | a0001c0001t0001g0147 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-158-3454_-158-345 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41120008 | |||||
| chrX:41120102
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0212 | 2 | NA18992.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-158-3369G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41120102 | ||||||
| chrX:41120244
|
T | TGATAC | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-158-3225_-158-322 others(9): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41120244 | |||||
| chrX:41120377
|
T | TTTTAAA | 1 | a0001c0001t0002g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-158-3093_-158-308 others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41120377 | |||||
| chrX:41120399
|
A | G | 1 | a0001c0001t0008g0137 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-158-3072A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41120399 | ||||||
| chrX:41120439
|
A | G | 1 | a0006c0007t0020g0098 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-158-3032A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41120439 | ||||||
| chrX:41120532
|
C | G | 4 | a0001c0002t0002g0196a0001c0002t0002g0215a0001c0002t0021g0195others(1): Show | 4 | HG03486.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-158-2939C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41120532 | ||||||
| chrX:41120607
|
C | T | 4 | a0001c0003t0001g0130a0001c0003t0001g0150a0001c0003t0001g0151others(1): Show | 4 | NA18954.hp2 NA18957.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-158-2864C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41120607 | ||||||
| chrX:41120659
|
C | T | 1 | a0001c0001t0003g0276 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-158-2812C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41120659 | ||||||
| chrX:41120683
|
A | G | 6 | a0001c0001t0002g0193a0001c0002t0002g0174a0001c0002t0002g0196others(3): Show | 6 | HG02615.hp1 HG02970.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-158-2788A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41120683 | ||||||
| chrX:41120734
|
A | G | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-158-2737A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41120734 | ||||||
| chrX:41120840
|
G | GT | 44 | a0001c0001t0001g0113a0001c0001t0001g0223a0001c0001t0001g0224others(41): Show | 44 | HG00323.hp1 HG00597.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.-158-2615dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41120840 | |||||
| chrX:41120840
|
G | GTT | 35 | a0001c0001t0002g0106a0001c0001t0003g0241a0001c0001t0003g0243others(32): Show | 35 | HG00423.hp1 HG00597.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.-158-2616_-158-261 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41120840 | |||||
| chrX:41120840
|
G | GTTT | 3 | a0001c0001t0002g0108a0001c0001t0003g0264a0001c0001t0004g0237 | 3 | HG01358.hp1 HG02738.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.-158-2617_-158-261 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41120840 | |||||
| chrX:41120840
|
GT | G | 3 | a0001c0001t0001g0131a0001c0001t0002g0062a0001c0001t0002g0083 | 3 | HG01943.hp1 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-158-2615delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41120840 | |||||
| chrX:41120844
|
T | G | 1 | a0001c0001t0026g0166 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-158-2627T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41120844 | ||||||
| chrX:41120998
|
C | T | 1 | a0001c0001t0002g0039 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-158-2473C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41120998 | ||||||
| chrX:41121005
|
A | AT | 60 | a0001c0001t0002g0037a0001c0001t0002g0059a0001c0001t0002g0065others(57): Show | 60 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-158-2452dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41121005 | |||||
| chrX:41121005
|
A | ATT | 2 | a0001c0001t0002g0038a0001c0001t0004g0266 | 2 | NA18945.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-158-2453_-158-245 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41121005 | |||||
| chrX:41121105
|
TC | T | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-158-2363delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41121105 | |||||
| chrX:41121128
|
C | T | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-158-2343C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41121128 | ||||||
| chrX:41121236
|
A | AG | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-158-2231dupG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41121236 | |||||
| chrX:41121324
|
C | T | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.-158-2147C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41121324 | ||||||
| chrX:41121622
|
G | A | 2 | a0001c0001t0013g0180a0001c0001t0028g0179 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-158-1849G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41121622 | ||||||
| chrX:41121646
|
G | GCC | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-158-1825_-158-182 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41121646 | ||||||
| chrX:41121649
|
C | T | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-158-1822C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41121649 | ||||||
| chrX:41121650
|
C | G | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-158-1821C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41121650 | ||||||
| chrX:41121683
|
A | C | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-158-1788A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41121683 | ||||||
| chrX:41121692
|
C | T | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-158-1779C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41121692 | ||||||
| chrX:41121760
|
C | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-158-1711C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41121760 | ||||||
| chrX:41121856
|
T | G | 1 | a0001c0001t0001g0221 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-158-1615T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41121856 | ||||||
| chrX:41121896
|
G | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-158-1575G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41121896 | ||||||
| chrX:41121899
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0200 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-158-1572C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41121899 | ||||||
| chrX:41122043
|
T | TA | 1 | a0001c0001t0030g0275 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-158-1428_-158-142 others(5): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41122043 | ||||||
| chrX:41122281
|
AC | A | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-158-1186delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41122281 | |||||
| chrX:41122410
|
TA | T | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-158-1055delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41122410 | |||||
| chrX:41122496
|
G | A | 6 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0048others(3): Show | 6 | HG02451.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-158-975G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41122496 | ||||||
| chrX:41122623
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-158-848C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41122623 | ||||||
| chrX:41122879
|
A | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-158-592A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41122879 | ||||||
| chrX:41122976
|
TG | T | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-158-491delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41122976 | |||||
| chrX:41123013
|
C | T | 1 | a0001c0001t0002g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-158-458C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41123013 | ||||||
| chrX:41123142
|
G | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-158-329G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41123142 | ||||||
| chrX:41123184
|
G | A | 13 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0046others(10): Show | 13 | HG00280.hp1 HG00733.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.-158-287G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41123184 | ||||||
| chrX:41123190
|
TA | T | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-158-279delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41123190 | |||||
| chrX:41123336
|
CT | C | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-158-130delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chrX | 41123336 | |||||
| chrX:41123388
|
C | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-158-83C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 1/44 | chrX | 41123388 | ||||||
| chrX:41123863
|
TG | T | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.96+141delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41123863 | |||||
| chrX:41123924
|
TC | T | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.96+203delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41123924 | |||||
| chrX:41123939
|
AG | A | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.96+217delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41123939 | |||||
| chrX:41123957
|
T | C | 197 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.96+233T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41123957 | ||||||
| chrX:41123967
|
TG | T | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.96+246delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41123967 | |||||
| chrX:41124164
|
C | T | 1 | a0001c0001t0002g0048 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.96+440C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41124164 | ||||||
| chrX:41124220
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.96+496C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41124220 | ||||||
| chrX:41124229
|
AG | A | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.96+507delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41124229 | |||||
| chrX:41124337
|
CG | C | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.96+616delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41124337 | |||||
| chrX:41124368
|
C | T | 1 | a0001c0001t0002g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.96+644C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41124368 | ||||||
| chrX:41124592
|
AG | A | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.96+873delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41124592 | |||||
| chrX:41125012
|
TGG | T | 1 | a0001c0001t0002g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.96+1289_96+1290del others(2): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125012 | ||||||
| chrX:41125016
|
A | G | 3 | a0001c0001t0003g0259a0001c0001t0003g0274a0001c0001t0031g0273 | 3 | HG02523.hp1 NA19063.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.96+1292A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125016 | ||||||
| chrX:41125047
|
G | T | 2 | a0001c0001t0013g0180a0001c0001t0028g0179 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.96+1323G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125047 | ||||||
| chrX:41125277
|
T | C | 4 | a0001c0001t0002g0015a0001c0001t0002g0094a0001c0001t0002g0095others(1): Show | 4 | HG02572.hp1 HG02818.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+1553T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125277 | ||||||
| chrX:41125330
|
CT | C | 1 | a0001c0001t0002g0108 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.96+1607delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125330 | ||||||
| chrX:41125367
|
A | AC | 3 | a0001c0001t0002g0071a0001c0001t0002g0108a0008c0006t0001g0002 | 3 | HG00438.hp1 HG02738.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.96+1646dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125367 | |||||
| chrX:41125373
|
C | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.96+1649C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125373 | ||||||
| chrX:41125380
|
AT | A | 197 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.96+1669delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125380 | |||||
| chrX:41125380
|
ATT | A | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.96+1668_96+1669del others(2): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125380 | |||||
| chrX:41125412
|
AT | A | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.96+1693delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125412 | |||||
| chrX:41125439
|
GTT | G | 1 | a0001c0001t0002g0084 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.96+1718_96+1719del others(2): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125439 | |||||
| chrX:41125467
|
G | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.96+1743G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125467 | ||||||
| chrX:41125469
|
A | T | 1 | a0001c0001t0001g0010 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.96+1745A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125469 | ||||||
| chrX:41125469
|
AT | A | 1 | a0001c0001t0004g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.96+1749delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125469 | |||||
| chrX:41125531
|
C | T | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.96+1807C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125531 | ||||||
| chrX:41125532
|
CTA | C | 1 | a0001c0001t0001g0132 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.96+1810_96+1811del others(2): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125532 | |||||
| chrX:41125607
|
C | G | 1 | a0001c0001t0001g0201 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.96+1883C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125607 | ||||||
| chrX:41125622
|
T | TC | 2 | a0001c0001t0002g0108a0001c0001t0005g0026 | 2 | HG02738.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.96+1904dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125622 | |||||
| chrX:41125630
|
CA | C | 1 | a0001c0001t0002g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.96+1907delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125630 | ||||||
| chrX:41125631
|
A | AC | 1 | a0001c0001t0005g0026 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.96+1911dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125631 | |||||
| chrX:41125643
|
A | AACACAC | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.96+1956_96+1961dup others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125643 | |||||
| chrX:41125643
|
A | AACACACA others(1): Show |
5 | a0001c0001t0001g0134a0001c0001t0001g0182a0001c0001t0001g0183others(2): Show | 5 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+1954_96+1961dup others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125643 | |||||
| chrX:41125643
|
A | AACACACA others(5): Show |
1 | a0001c0001t0001g0129 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.96+1950_96+1961dup others(12): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125643 | |||||
| chrX:41125643
|
A | AACACACA others(9): Show |
1 | a0001c0001t0006g0148 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.96+1946_96+1961dup others(16): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125643 | |||||
| chrX:41125643
|
A | AC | 4 | a0001c0001t0001g0145a0001c0001t0002g0036a0001c0001t0002g0076others(1): Show | 4 | HG00408.hp1 HG01069.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+1919_96+1920ins others(1): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125643 | ||||||
| chrX:41125643
|
AAC | A | 4 | a0001c0001t0002g0057a0001c0001t0005g0063a0001c0001t0007g0044others(1): Show | 4 | HG01175.hp1 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+1960_96+1961del others(2): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125643 | |||||
| chrX:41125643
|
AACACAC | A | 3 | a0001c0001t0002g0075a0001c0001t0003g0282a0001c0001t0003g0283 | 3 | HG03688.hp1 NA18964.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.96+1956_96+1961del others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125643 | |||||
| chrX:41125643
|
AACACACA others(1): Show |
A | 1 | a0001c0001t0003g0285 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.96+1954_96+1961del others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125643 | |||||
| chrX:41125643
|
AACACACA others(3): Show |
A | 4 | a0001c0001t0003g0241a0001c0001t0003g0289a0001c0001t0003g0291others(1): Show | 4 | HG02698.hp1 NA18957.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+1952_96+1961del others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125643 | |||||
| chrX:41125643
|
AACACACA others(5): Show |
A | 11 | a0001c0001t0003g0239a0001c0001t0003g0243a0001c0001t0003g0276others(8): Show | 11 | HG00323.hp1 HG02004.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.96+1950_96+1961del others(12): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125643 | |||||
| chrX:41125643
|
AACACACA others(7): Show |
A | 3 | a0001c0001t0003g0238a0001c0001t0003g0244a0001c0001t0003g0254 | 3 | HG02630.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.96+1948_96+1961del others(14): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125643 | |||||
| chrX:41125670
|
ACACACAC others(9): Show |
A | 1 | a0001c0001t0033g0240 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.96+1948_96+1963del others(16): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125670 | |||||
| chrX:41125670
|
ACACACAC others(17): Show |
A | 3 | a0001c0001t0003g0253a0001c0001t0004g0255a0001c0001t0004g0277 | 3 | HG04184.hp1 NA18968.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.96+1948_96+1971del others(24): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125670 | |||||
| chrX:41125670
|
ACACACAC others(19): Show |
A | 28 | a0001c0001t0003g0250a0001c0001t0003g0261a0001c0001t0003g0263others(25): Show | 28 | HG00423.hp1 HG00597.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.96+1948_96+1973del others(26): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125670 | |||||
| chrX:41125672
|
ACACACAC others(11): Show |
A | 1 | a0001c0001t0003g0288 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.96+1950_96+1967del others(18): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125672 | |||||
| chrX:41125672
|
ACACACAC others(17): Show |
A | 2 | a0001c0001t0003g0259a0001c0001t0031g0273 | 2 | HG02523.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.96+1950_96+1973del others(24): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125672 | |||||
| chrX:41125676
|
A | ACTCTCT | 1 | a0001c0002t0021g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.96+1953_96+1954ins others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125676 | |||||
| chrX:41125678
|
A | ACTCT | 1 | a0001c0008t0002g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.96+1955_96+1956ins others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125678 | |||||
| chrX:41125678
|
A | ACTCTCTC others(1): Show |
3 | a0001c0002t0002g0121a0001c0002t0002g0196a0001c0002t0002g0215 | 3 | HG02717.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.96+1955_96+1956ins others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125678 | |||||
| chrX:41125678
|
A | ACTCTCTC others(5): Show |
1 | a0001c0002t0002g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.96+1955_96+1956ins others(12): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125678 | |||||
| chrX:41125678
|
A | T | 2 | a0001c0001t0002g0075a0001c0002t0021g0195 | 2 | NA18906.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.96+1954A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125678 | ||||||
| chrX:41125680
|
A | ACT | 3 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0007g0020 | 3 | HG01168.hp1 NA18979.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.96+1957_96+1958ins others(2): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125680 | |||||
| chrX:41125680
|
A | ACTCT | 7 | a0001c0001t0002g0042a0001c0001t0002g0046a0001c0001t0002g0058others(4): Show | 7 | HG00733.hp2 HG01255.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+1957_96+1958ins others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125680 | |||||
| chrX:41125680
|
A | ACTCTCT | 5 | a0001c0001t0002g0035a0001c0001t0002g0056a0001c0001t0002g0083others(2): Show | 5 | HG02647.hp1 HG03130.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+1957_96+1958ins others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125680 | |||||
| chrX:41125680
|
A | ACTCTCTC others(1): Show |
4 | a0001c0001t0002g0011a0001c0002t0002g0118a0001c0002t0002g0119others(1): Show | 4 | HG02165.hp2 HG02258.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+1957_96+1958ins others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125680 | |||||
| chrX:41125680
|
A | ACTCTCTC others(3): Show |
2 | a0001c0002t0002g0120a0005c0011t0002g0117 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.96+1957_96+1958ins others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125680 | |||||
| chrX:41125680
|
A | T | 9 | a0001c0001t0002g0075a0001c0001t0003g0282a0001c0001t0007g0017others(6): Show | 9 | HG00280.hp1 HG01891.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+1956A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125680 | ||||||
| chrX:41125682
|
A | ACT | 9 | a0001c0001t0002g0037a0001c0001t0002g0047a0001c0001t0005g0012others(6): Show | 9 | HG02602.hp1 HG03017.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+1959_96+1960ins others(2): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125682 | |||||
| chrX:41125682
|
A | ACTCT | 16 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0040others(13): Show | 16 | HG00438.hp1 HG01123.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.96+1959_96+1960ins others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125682 | |||||
| chrX:41125682
|
A | ACTCTCT | 5 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0002g0055others(2): Show | 5 | HG02976.hp1 HG06807.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+1959_96+1960ins others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125682 | |||||
| chrX:41125682
|
A | ACTCTCTC others(1): Show |
1 | a0001c0002t0002g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.96+1959_96+1960ins others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125682 | |||||
| chrX:41125682
|
A | ACTCTCTC others(3): Show |
2 | a0001c0001t0002g0086a0001c0001t0002g0193 | 2 | HG01928.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.96+1959_96+1960ins others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125682 | |||||
| chrX:41125682
|
A | T | 37 | a0001c0001t0002g0011a0001c0001t0002g0034a0001c0001t0002g0035others(34): Show | 37 | HG00280.hp1 HG00733.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.96+1958A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125682 | ||||||
| chrX:41125682
|
ACACT | A | 1 | a0001c0001t0002g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.96+1960_96+1963del others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125682 | |||||
| chrX:41125684
|
A | ACACACAC others(31): Show |
1 | a0001c0001t0001g0147 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(38): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(35): Show |
1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(42): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(39): Show |
1 | a0001c0001t0001g0146 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(46): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(21): Show |
1 | a0001c0001t0016g0185 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(28): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(29): Show |
1 | a0001c0001t0001g0149 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(36): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(31): Show |
2 | a0001c0003t0001g0130a0001c0003t0001g0150 | 2 | NA18954.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(38): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(17): Show |
1 | a0001c0001t0001g0006 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(24): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(27): Show |
1 | a0001c0001t0001g0201 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(34): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(13): Show |
2 | a0001c0001t0001g0140a0001c0001t0001g0226 | 2 | HG01891.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(20): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(15): Show |
3 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0006g0008 | 3 | HG02155.hp1 NA18984.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(22): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(17): Show |
1 | a0001c0001t0001g0171 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(24): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(19): Show |
1 | a0001c0001t0010g0156 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(26): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(29): Show |
1 | a0001c0003t0001g0151 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(36): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(11): Show |
1 | a0001c0001t0001g0212 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(18): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(13): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0111 | 2 | NA18961.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(20): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(15): Show |
1 | a0001c0001t0001g0003 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(22): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(17): Show |
3 | a0001c0001t0001g0143a0001c0001t0001g0198a0001c0001t0001g0232 | 3 | HG01071.hp2 HG03486.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(24): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(19): Show |
1 | a0001c0001t0001g0009 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(26): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(21): Show |
1 | a0001c0001t0001g0199 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(28): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(23): Show |
1 | a0001c0001t0008g0136 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(30): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(25): Show |
1 | a0001c0001t0013g0180 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(32): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(9): Show |
1 | a0001c0001t0001g0186 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(16): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(11): Show |
4 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0189others(1): Show | 4 | HG02074.hp1 HG02809.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(18): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(13): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0194a0001c0001t0008g0135 | 3 | HG01168.hp2 NA18951.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(20): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(15): Show |
6 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0188others(3): Show | 6 | HG01069.hp1 HG02055.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(22): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(19): Show |
1 | a0001c0001t0001g0010 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(26): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(23): Show |
1 | a0001c0001t0008g0103 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(30): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(25): Show |
1 | a0001c0001t0008g0142 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(32): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(9): Show |
1 | a0001c0001t0002g0106 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(16): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(11): Show |
2 | a0001c0001t0001g0112a0001c0001t0001g0202 | 2 | HG00438.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(18): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(13): Show |
4 | a0001c0001t0001g0154a0001c0001t0001g0161a0001c0001t0001g0192others(1): Show | 4 | HG03654.hp1 HG04199.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(20): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(15): Show |
4 | a0001c0001t0001g0139a0001c0001t0001g0172a0001c0001t0010g0157others(1): Show | 4 | HG00738.hp1 HG01978.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(22): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(17): Show |
1 | a0001c0001t0001g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(24): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(23): Show |
3 | a0001c0001t0001g0153a0001c0001t0001g0206a0001c0001t0008g0137 | 3 | HG03490.hp1 NA18973.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(30): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(5): Show |
4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(1): Show | 4 | HG00099.hp2 HG01515.hp1 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(12): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(9): Show |
3 | a0001c0001t0001g0190a0001c0001t0001g0197a0001c0001t0001g0219 | 3 | HG00733.hp1 HG02280.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(16): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(11): Show |
6 | a0001c0001t0001g0167a0001c0001t0001g0187a0001c0001t0002g0108others(3): Show | 6 | HG00408.hp2 HG00558.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(18): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(13): Show |
2 | a0001c0001t0001g0155a0001c0001t0001g0228 | 2 | HG01106.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(20): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(15): Show |
3 | a0001c0001t0001g0163a0001c0001t0001g0209a0001c0001t0001g0225 | 3 | HG02683.hp2 HG02922.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(22): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(17): Show |
2 | a0001c0001t0001g0164a0001c0001t0001g0191 | 2 | HG00609.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(24): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(29): Show |
1 | a0001c0001t0028g0179 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(36): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(7): Show |
4 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0181others(1): Show | 4 | HG02004.hp2 HG02056.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(14): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(9): Show |
7 | a0001c0001t0001g0127a0001c0001t0001g0138a0001c0001t0001g0159others(4): Show | 7 | HG01081.hp1 HG01123.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(16): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(11): Show |
4 | a0001c0001t0001g0162a0001c0001t0001g0173a0001c0001t0001g0214others(1): Show | 4 | HG00558.hp1 HG03139.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(18): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(13): Show |
1 | a0001c0001t0001g0132 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(20): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(17): Show |
1 | a0001c0001t0001g0205 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(24): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(5): Show |
1 | a0001c0001t0024g0234 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(12): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(7): Show |
5 | a0001c0001t0001g0131a0001c0001t0012g0082a0001c0004t0002g0177others(2): Show | 5 | HG01943.hp1 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(14): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(9): Show |
2 | a0001c0001t0001g0168a0001c0001t0027g0104 | 2 | HG02129.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(16): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(11): Show |
1 | a0001c0001t0001g0221 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(18): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACAC others(13): Show |
2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG02148.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(20): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACTC others(3): Show |
4 | a0001c0001t0001g0144a0001c0001t0001g0169a0001c0001t0002g0050others(1): Show | 4 | HG00423.hp2 HG00597.hp1 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACTC others(7): Show |
2 | a0001c0001t0001g0203a0001c0001t0001g0224 | 2 | HG02976.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(14): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACACTC others(9): Show |
1 | a0001c0001t0001g0170 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(16): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACTCTC others(3): Show |
3 | a0001c0001t0001g0217a0001c0001t0002g0027a0001c0001t0002g0072 | 3 | HG00673.hp1 HG02809.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.96+1961_96+1962ins others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACTCTC others(5): Show |
1 | a0001c0001t0002g0060 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(12): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACACTCTC others(7): Show |
1 | a0001c0001t0001g0115 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.96+1961_96+1962ins others(14): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACT | 1 | a0001c0001t0023g0022 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.96+1994_96+1995dup others(2): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACTCT | 6 | a0001c0001t0002g0019a0001c0001t0005g0090a0001c0001t0007g0043others(3): Show | 6 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+1992_96+1995dup others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACTCTCT | 10 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0036others(7): Show | 10 | HG00408.hp1 HG00621.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+1990_96+1995dup others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACTCTCTC others(1): Show |
8 | a0001c0001t0002g0015a0001c0001t0002g0024a0001c0001t0002g0030others(5): Show | 8 | HG01081.hp2 HG02109.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+1988_96+1995dup others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACTCTCTC others(3): Show |
1 | a0001c0001t0009g0233 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.96+1986_96+1995dup others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | ACTCTCTC others(7): Show |
1 | a0001c0001t0001g0152 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.96+1982_96+1995dup others(14): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125684
|
A | T | 79 | a0001c0001t0002g0011a0001c0001t0002g0013a0001c0001t0002g0031others(76): Show | 79 | HG00280.hp1 HG00438.hp1 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.96+1960A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125684 | ||||||
| chrX:41125684
|
ACT | A | 2 | a0001c0001t0005g0091a0001c0001t0005g0092 | 2 | HG02148.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.96+1994_96+1995del others(2): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125684 | |||||
| chrX:41125686
|
T | A | 4 | a0001c0001t0001g0134a0001c0001t0006g0148a0002c0005t0011g0235others(1): Show | 4 | HG06807.hp1 NA18939.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+1962T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125686 | ||||||
| chrX:41125688
|
T | A | 4 | a0001c0001t0001g0134a0001c0001t0006g0148a0002c0005t0011g0235others(1): Show | 4 | HG06807.hp1 NA18939.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+1964T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125688 | ||||||
| chrX:41125690
|
T | A | 4 | a0001c0001t0001g0134a0001c0001t0006g0148a0002c0005t0011g0235others(1): Show | 4 | HG06807.hp1 NA18939.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+1966T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125690 | ||||||
| chrX:41125692
|
T | A | 2 | a0001c0001t0001g0134a0001c0001t0006g0148 | 2 | NA18939.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.96+1968T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125692 | ||||||
| chrX:41125701
|
C | CTCTCTCT | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.96+1978_96+1984dup others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125701 | |||||
| chrX:41125705
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.96+1981C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125705 | ||||||
| chrX:41125718
|
T | G | 3 | a0001c0001t0003g0238a0001c0001t0003g0243a0001c0001t0003g0244 | 3 | HG02145.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.96+1994T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125718 | ||||||
| chrX:41125718
|
T | TCG | 1 | a0001c0001t0001g0229 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.96+1998_96+1999dup others(2): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125718 | |||||
| chrX:41125718
|
T | TCGCG | 8 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG01167.hp1 HG01891.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+1996_96+1999dup others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125718 | |||||
| chrX:41125722
|
G | GCA | 1 | a0001c0001t0002g0069 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.96+2000_96+2001dup others(2): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125722 | |||||
| chrX:41125724
|
A | AC | 3 | a0001c0001t0001g0189a0001c0001t0009g0233a0001c0001t0016g0185 | 3 | HG00741.hp2 HG01099.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.96+2001dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125724 | |||||
| chrX:41125724
|
A | ACAG | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.96+2001_96+2002ins others(3): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125724 | |||||
| chrX:41125724
|
A | ACG | 22 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0160others(19): Show | 22 | HG00597.hp1 HG01496.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+2010_96+2011dup others(2): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125724 | |||||
| chrX:41125724
|
A | AG | 1 | a0001c0001t0001g0115 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.96+2000_96+2001ins others(1): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125724 | ||||||
| chrX:41125725
|
C | CA | 5 | a0001c0001t0001g0007a0001c0001t0001g0145a0001c0001t0002g0101others(2): Show | 5 | HG01069.hp1 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+2001_96+2002ins others(1): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125725 | ||||||
| chrX:41125729
|
C | CA | 2 | a0001c0001t0001g0163a0008c0006t0001g0002 | 2 | NA18953.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.96+2005_96+2006ins others(1): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125729 | ||||||
| chrX:41125729
|
C | CG | 1 | a0001c0001t0003g0269 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.96+2006dupG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125729 | |||||
| chrX:41125731
|
C | CA | 4 | a0001c0001t0001g0007a0001c0001t0001g0127a0001c0001t0002g0076others(1): Show | 4 | HG01123.hp1 NA18943.hp1 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+2007_96+2008ins others(1): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125731 | ||||||
| chrX:41125731
|
C | CGA | 1 | a0001c0001t0005g0026 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.96+2008_96+2009ins others(2): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125731 | |||||
| chrX:41125732
|
G | GC | 1 | a0001c0001t0005g0080 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.96+2009dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125732 | |||||
| chrX:41125733
|
C | CA | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.96+2009_96+2010ins others(1): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125733 | ||||||
| chrX:41125734
|
G | GCGCT | 1 | a0001c0001t0002g0108 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.96+2011_96+2012ins others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125734 | |||||
| chrX:41125758
|
GCTTA | G | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.96+2038_96+2041del others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41125758 | |||||
| chrX:41125793
|
A | G | 8 | a0001c0002t0002g0118a0001c0002t0002g0119a0001c0002t0002g0120others(5): Show | 8 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+2069A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125793 | ||||||
| chrX:41125898
|
C | G | 1 | a0001c0001t0001g0230 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.96+2174C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41125898 | ||||||
| chrX:41126407
|
GTAGT | G | 2 | a0001c0001t0013g0180a0001c0001t0028g0179 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.97-2589_97-2586del others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41126407 | |||||
| chrX:41126610
|
A | G | 35 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(32): Show | 35 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.97-2390A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41126610 | ||||||
| chrX:41126990
|
C | T | 2 | a0001c0001t0003g0269a0001c0001t0003g0271 | 2 | NA19066.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.97-2010C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41126990 | ||||||
| chrX:41127767
|
G | A | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.97-1233G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41127767 | ||||||
| chrX:41127779
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.97-1221A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41127779 | ||||||
| chrX:41127895
|
G | C | 16 | a0001c0001t0001g0115a0001c0001t0001g0147a0001c0001t0001g0152others(13): Show | 16 | HG02027.hp1 HG02523.hp2 HG04115.hp1 others(13): Show |
intron_variant | MODIFIER | c.97-1105G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41127895 | ||||||
| chrX:41128207
|
CAG | C | 2 | a0001c0001t0003g0292a0001c0002t0002g0121 | 2 | HG02717.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.97-791_97-790delGA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41128207 | |||||
| chrX:41128380
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.97-620T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41128380 | ||||||
| chrX:41128407
|
GT | G | 92 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0138others(89): Show | 92 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.97-585delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chrX | 41128407 | |||||
| chrX:41128734
|
A | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG00423.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.97-266A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41128734 | ||||||
| chrX:41128935
|
G | A | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.97-65G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 2/44 | chrX | 41128935 | ||||||
| chrX:41130298
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.242+1153C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | chrX | 41130298 | ||||||
| chrX:41130431
|
CAG | C | 1 | a0001c0001t0004g0258 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.243-1025_243-1024d others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | chrX | 41130431 | ||||||
| chrX:41130454
|
AT | A | 1 | a0001c0001t0001g0230 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.243-993delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chrX | 41130454 | |||||
| chrX:41130465
|
C | CT | 1 | a0001c0001t0002g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.243-985dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chrX | 41130465 | |||||
| chrX:41130473
|
C | CT | 12 | a0001c0001t0001g0163a0001c0001t0001g0192a0001c0001t0001g0223others(9): Show | 12 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.243-973dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chrX | 41130473 | |||||
| chrX:41130473
|
CT | C | 1 | a0001c0001t0002g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.243-973delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chrX | 41130473 | |||||
| chrX:41130478
|
TTTTTTTG | T | 1 | a0001c0001t0028g0179 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.243-958_243-952del others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chrX | 41130478 | |||||
| chrX:41130479
|
TTTTTTGT others(6): Show |
T | 2 | a0001c0001t0003g0241a0001c0001t0004g0256 | 2 | NA18941.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.243-972_243-960del others(13): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chrX | 41130479 | |||||
| chrX:41130485
|
GTTTTTTG others(8): Show |
G | 57 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(54): Show | 57 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.243-965_243-951del others(15): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chrX | 41130485 | |||||
| chrX:41130499
|
GT | G | 2 | a0001c0001t0003g0241a0001c0001t0004g0256 | 2 | NA18941.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.243-950delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chrX | 41130499 | |||||
| chrX:41130508
|
G | A | 14 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(11): Show | 14 | HG00323.hp1 HG02004.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.243-949G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | chrX | 41130508 | ||||||
| chrX:41130523
|
T | C | 1 | a0001c0001t0002g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.243-934T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | chrX | 41130523 | ||||||
| chrX:41130591
|
C | T | 1 | a0001c0001t0005g0066 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.243-866C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | chrX | 41130591 | ||||||
| chrX:41130727
|
C | CT | 58 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.243-720dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chrX | 41130727 | |||||
| chrX:41130851
|
G | A | 1 | a0001c0001t0002g0039 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.243-606G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | chrX | 41130851 | ||||||
| chrX:41130914
|
C | T | 2 | a0001c0001t0004g0242a0001c0001t0004g0257 | 2 | HG01074.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.243-543C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | chrX | 41130914 | ||||||
| chrX:41131021
|
C | CA | 1 | a0001c0001t0005g0026 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.243-436_243-435ins others(1): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | chrX | 41131021 | ||||||
| chrX:41131041
|
C | CA | 3 | a0001c0001t0001g0154a0001c0001t0003g0271a0001c0001t0005g0066 | 3 | HG02602.hp1 NA19083.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.243-405dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chrX | 41131041 | |||||
| chrX:41131052
|
A | AG | 7 | a0001c0001t0001g0140a0001c0001t0001g0163a0001c0001t0001g0203others(4): Show | 7 | HG00621.hp1 HG04115.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.243-399dupG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chrX | 41131052 | |||||
| chrX:41131068
|
A | G | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.243-389A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | chrX | 41131068 | ||||||
| chrX:41131139
|
A | G | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.243-318A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | chrX | 41131139 | ||||||
| chrX:41131215
|
A | T | 1 | a0001c0001t0001g0162 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.243-242A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | chrX | 41131215 | ||||||
| chrX:41131284
|
G | T | 33 | a0001c0001t0003g0250a0001c0001t0003g0253a0001c0001t0003g0259others(30): Show | 33 | HG00423.hp1 HG00597.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.243-173G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | chrX | 41131284 | ||||||
| chrX:41131305
|
A | T | 1 | a0001c0001t0004g0278 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.243-152A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | chrX | 41131305 | ||||||
| chrX:41131388
|
G | A | 2 | a0001c0001t0003g0269a0001c0001t0003g0271 | 2 | NA19066.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.243-69G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 3/44 | chrX | 41131388 | ||||||
| chrX:41132037
|
C | G | 10 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(7): Show | 10 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.322+501C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | chrX | 41132037 | ||||||
| chrX:41132178
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | NA18951.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.322+642A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | chrX | 41132178 | ||||||
| chrX:41132263
|
T | C | 1 | a0001c0001t0002g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.322+727T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | chrX | 41132263 | ||||||
| chrX:41132279
|
G | A | 1 | a0001c0001t0010g0156 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.322+743G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | chrX | 41132279 | ||||||
| chrX:41132295
|
A | AT | 51 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(48): Show | 51 | HG00423.hp1 HG00597.hp2 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.322+784dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 41132295 | |||||
| chrX:41132295
|
A | ATT | 4 | a0001c0001t0004g0265a0001c0001t0004g0268a0001c0001t0004g0270others(1): Show | 4 | HG01175.hp2 HG01978.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.322+783_322+784dup others(2): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 41132295 | |||||
| chrX:41132295
|
AT | A | 83 | a0001c0001t0001g0006a0001c0001t0002g0011a0001c0001t0002g0015others(80): Show | 83 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.322+784delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 41132295 | |||||
| chrX:41132295
|
ATT | A | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.322+783_322+784del others(2): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 41132295 | |||||
| chrX:41132295
|
ATTT | A | 9 | a0001c0001t0001g0114a0001c0001t0001g0182a0001c0001t0001g0224others(6): Show | 9 | HG00140.hp1 HG01070.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.322+782_322+784del others(3): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 41132295 | |||||
| chrX:41132295
|
ATTTTTTT others(2): Show |
A | 1 | a0001c0001t0005g0066 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.322+776_322+784del others(9): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 41132295 | |||||
| chrX:41132295
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0158 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.322+771_322+784del others(14): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 41132295 | |||||
| chrX:41132295
|
ATTTTTTT others(8): Show |
A | 73 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0131others(70): Show | 73 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.322+770_322+784del others(15): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 41132295 | |||||
| chrX:41132501
|
A | G | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.322+965A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | chrX | 41132501 | ||||||
| chrX:41132568
|
T | A | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.322+1032T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | chrX | 41132568 | ||||||
| chrX:41132610
|
TTTTC | T | 1 | a0001c0001t0003g0283 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.322+1090_322+1093d others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 41132610 | |||||
| chrX:41132626
|
C | CT | 1 | a0001c0001t0004g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.322+1100dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 41132626 | |||||
| chrX:41132689
|
T | C | 3 | a0001c0001t0001g0197a0001c0001t0001g0218a0001c0001t0001g0219 | 3 | HG02055.hp1 HG02280.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.322+1153T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | chrX | 41132689 | ||||||
| chrX:41132750
|
A | AT | 1 | a0001c0001t0001g0194 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.322+1227dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 41132750 | |||||
| chrX:41132750
|
AT | A | 60 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(57): Show | 60 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.322+1227delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 41132750 | |||||
| chrX:41132849
|
TG | T | 1 | a0001c0001t0004g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.322+1315delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 41132849 | |||||
| chrX:41132899
|
C | CT | 1 | a0001c0001t0002g0101 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.322+1371dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 41132899 | |||||
| chrX:41132932
|
AG | A | 1 | a0001c0001t0004g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.322+1398delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 41132932 | |||||
| chrX:41132978
|
T | C | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.322+1442T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | chrX | 41132978 | ||||||
| chrX:41133066
|
A | C | 6 | a0001c0001t0002g0193a0001c0002t0002g0174a0001c0002t0002g0196others(3): Show | 6 | HG02615.hp1 HG02970.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.322+1530A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | chrX | 41133066 | ||||||
| chrX:41133140
|
C | T | 1 | a0001c0001t0013g0180 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.323-1585C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | chrX | 41133140 | ||||||
| chrX:41133246
|
A | G | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.323-1479A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | chrX | 41133246 | ||||||
| chrX:41133692
|
T | G | 1 | a0001c0001t0001g0006 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.323-1033T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | chrX | 41133692 | ||||||
| chrX:41133820
|
A | T | 1 | a0001c0001t0001g0214 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.323-905A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | chrX | 41133820 | ||||||
| chrX:41134062
|
A | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.323-663A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | chrX | 41134062 | ||||||
| chrX:41134081
|
A | G | 14 | a0001c0001t0002g0193a0001c0002t0002g0118a0001c0002t0002g0119others(11): Show | 14 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.323-644A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | chrX | 41134081 | ||||||
| chrX:41134101
|
C | G | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.323-624C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | chrX | 41134101 | ||||||
| chrX:41134143
|
A | AC | 1 | a0001c0001t0004g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.323-580dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 41134143 | |||||
| chrX:41134453
|
A | G | 193 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.323-272A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | chrX | 41134453 | ||||||
| chrX:41134654
|
T | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.323-71T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | chrX | 41134654 | ||||||
| chrX:41134685
|
G | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.323-40G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | chrX | 41134685 | ||||||
| chrX:41134694
|
G | GT | 1 | a0001c0001t0004g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.323-28dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 41134694 | |||||
| chrX:41135291
|
C | T | 5 | a0001c0001t0002g0019a0001c0001t0002g0040a0001c0001t0009g0025others(2): Show | 5 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.435+454C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 5/44 | chrX | 41135291 | ||||||
| chrX:41135342
|
A | G | 2 | a0001c0001t0001g0138a0001c0001t0001g0200 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.435+505A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 5/44 | chrX | 41135342 | ||||||
| chrX:41135471
|
C | T | 1 | a0001c0001t0002g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.435+634C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 5/44 | chrX | 41135471 | ||||||
| chrX:41135475
|
TC | T | 1 | a0001c0001t0004g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.435+640delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 5/44 | INFO_REALIGN_3_PRIME | chrX | 41135475 | |||||
| chrX:41135641
|
C | A | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.435+804C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 5/44 | chrX | 41135641 | ||||||
| chrX:41135684
|
G | A | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.435+847G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 5/44 | chrX | 41135684 | ||||||
| chrX:41135717
|
G | A | 4 | a0001c0001t0002g0210a0001c0004t0002g0177a0001c0004t0002g0178others(1): Show | 4 | HG02615.hp2 HG02723.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+880G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 5/44 | chrX | 41135717 | ||||||
| chrX:41135794
|
C | T | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.435+957C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 5/44 | chrX | 41135794 | ||||||
| chrX:41135974
|
C | G | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.436-830C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 5/44 | chrX | 41135974 | ||||||
| chrX:41135983
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.436-821T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 5/44 | chrX | 41135983 | ||||||
| chrX:41136053
|
T | A | 1 | a0001c0001t0005g0051 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.436-751T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 5/44 | chrX | 41136053 | ||||||
| chrX:41136362
|
T | C | 1 | a0001c0001t0001g0125 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.436-442T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 5/44 | chrX | 41136362 | ||||||
| chrX:41136420
|
C | G | 6 | a0001c0001t0002g0193a0001c0002t0002g0174a0001c0002t0002g0196others(3): Show | 6 | HG02615.hp1 HG02970.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.436-384C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 5/44 | chrX | 41136420 | ||||||
| chrX:41136502
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.436-302A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 5/44 | chrX | 41136502 | ||||||
| chrX:41136567
|
T | A | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.436-237T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 5/44 | chrX | 41136567 | ||||||
| chrX:41136764
|
G | GT | 1 | a0006c0007t0020g0098 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.436-36dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 5/44 | INFO_REALIGN_3_PRIME | chrX | 41136764 | |||||
| chrX:41137032
|
TTTG | T | 1 | a0001c0001t0001g0207 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.654+13_654+15delGT others(1): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41137032 | |||||
| chrX:41137055
|
A | G | 1 | a0001c0001t0008g0137 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.654+33A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | chrX | 41137055 | ||||||
| chrX:41137060
|
A | G | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.654+38A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | chrX | 41137060 | ||||||
| chrX:41137184
|
GT | G | 1 | a0006c0007t0020g0098 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.654+168delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41137184 | |||||
| chrX:41137258
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.654+236T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | chrX | 41137258 | ||||||
| chrX:41137348
|
AT | A | 1 | a0006c0007t0020g0098 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.654+330delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41137348 | |||||
| chrX:41137496
|
G | GT | 1 | a0006c0007t0020g0098 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.654+478dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41137496 | |||||
| chrX:41137582
|
A | C | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.654+560A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | chrX | 41137582 | ||||||
| chrX:41137614
|
AT | A | 1 | a0006c0007t0020g0098 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.654+594delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41137614 | |||||
| chrX:41137616
|
T | TA | 1 | a0001c0001t0002g0065 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.654+595dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41137616 | |||||
| chrX:41137717
|
C | CA | 1 | a0001c0001t0004g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.654+702dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41137717 | |||||
| chrX:41137777
|
C | G | 3 | a0001c0001t0005g0051a0001c0001t0005g0052a0001c0001t0005g0054 | 3 | HG03017.hp1 HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.654+755C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | chrX | 41137777 | ||||||
| chrX:41137830
|
G | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.654+808G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | chrX | 41137830 | ||||||
| chrX:41137841
|
G | GA | 1 | a0001c0001t0002g0065 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.654+823dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41137841 | |||||
| chrX:41137881
|
CT | C | 4 | a0001c0001t0001g0154a0001c0004t0002g0177a0001c0004t0002g0178others(1): Show | 4 | HG02723.hp2 HG02896.hp1 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+870delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41137881 | |||||
| chrX:41137884
|
T | C | 1 | a0001c0001t0002g0083 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.654+862T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | chrX | 41137884 | ||||||
| chrX:41138025
|
A | AT | 1 | a0001c0001t0002g0065 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.654+1005dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41138025 | |||||
| chrX:41138047
|
AT | A | 1 | a0001c0001t0004g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.654+1027delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41138047 | |||||
| chrX:41138072
|
GC | G | 1 | a0001c0001t0004g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.654+1052delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41138072 | |||||
| chrX:41138087
|
AT | A | 1 | a0006c0007t0020g0098 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.654+1070delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41138087 | |||||
| chrX:41138110
|
T | TA | 1 | a0001c0001t0002g0065 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.654+1089dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41138110 | |||||
| chrX:41138305
|
A | C | 2 | a0001c0001t0002g0062a0001c0001t0002g0083 | 2 | HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.654+1283A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | chrX | 41138305 | ||||||
| chrX:41138334
|
G | GT | 1 | a0001c0001t0004g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.654+1319dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41138334 | |||||
| chrX:41138509
|
T | G | 1 | a0001c0001t0001g0139 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.654+1487T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | chrX | 41138509 | ||||||
| chrX:41138581
|
C | CA | 1 | a0006c0007t0020g0098 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.654+1560dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41138581 | |||||
| chrX:41138637
|
C | T | 4 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(1): Show | 4 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+1615C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | chrX | 41138637 | ||||||
| chrX:41138777
|
T | TC | 1 | a0006c0007t0020g0098 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.654+1756dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41138777 | |||||
| chrX:41138802
|
CT | C | 1 | a0006c0007t0020g0098 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.654+1783delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41138802 | |||||
| chrX:41138869
|
T | TG | 1 | a0001c0001t0002g0065 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.655-1785dupG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41138869 | |||||
| chrX:41138888
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.655-1768A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | chrX | 41138888 | ||||||
| chrX:41138952
|
GT | G | 1 | a0006c0007t0020g0098 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.655-1702delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41138952 | |||||
| chrX:41139005
|
GA | G | 1 | a0001c0001t0004g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.655-1649delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41139005 | |||||
| chrX:41139329
|
GA | G | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.655-1324delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41139329 | |||||
| chrX:41139344
|
C | CA | 1 | a0001c0001t0004g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.655-1311dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41139344 | |||||
| chrX:41139418
|
TG | T | 1 | a0001c0001t0004g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.655-1235delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41139418 | |||||
| chrX:41139646
|
T | TA | 1 | a0006c0007t0020g0098 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.655-1006dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41139646 | |||||
| chrX:41139678
|
G | C | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.655-978G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | chrX | 41139678 | ||||||
| chrX:41139771
|
T | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.655-885T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | chrX | 41139771 | ||||||
| chrX:41139850
|
TA | T | 1 | a0006c0007t0020g0098 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.655-802delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41139850 | |||||
| chrX:41140238
|
A | G | 1 | a0006c0007t0020g0098 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.655-418A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | chrX | 41140238 | ||||||
| chrX:41140258
|
A | G | 13 | a0001c0002t0002g0118a0001c0002t0002g0119a0001c0002t0002g0120others(10): Show | 13 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.655-398A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | chrX | 41140258 | ||||||
| chrX:41140340
|
A | C | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.655-316A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | chrX | 41140340 | ||||||
| chrX:41140413
|
A | AC | 1 | a0001c0001t0004g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.655-241dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | INFO_REALIGN_3_PRIME | chrX | 41140413 | |||||
| chrX:41140431
|
G | A | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.655-225G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | chrX | 41140431 | ||||||
| chrX:41140475
|
G | A | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.655-181G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | chrX | 41140475 | ||||||
| chrX:41140600
|
C | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.655-56C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 6/44 | chrX | 41140600 | ||||||
| chrX:41141493
|
G | A | 1 | a0001c0001t0003g0288 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1161+62G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 9/44 | chrX | 41141493 | ||||||
| chrX:41141624
|
A | G | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1161+193A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 9/44 | chrX | 41141624 | ||||||
| chrX:41141725
|
A | AG | 1 | a0006c0007t0020g0098 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1161+296dupG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 9/44 | INFO_REALIGN_3_PRIME | chrX | 41141725 | |||||
| chrX:41141795
|
A | C | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1161+364A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 9/44 | chrX | 41141795 | ||||||
| chrX:41141966
|
GAGTA | G | 1 | a0001c0002t0021g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1161+540_1161+543d others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 9/44 | INFO_REALIGN_3_PRIME | chrX | 41141966 | |||||
| chrX:41142029
|
G | C | 1 | a0001c0001t0027g0104 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1161+598G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 9/44 | chrX | 41142029 | ||||||
| chrX:41142135
|
T | C | 1 | a0001c0001t0023g0022 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1161+704T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 9/44 | chrX | 41142135 | ||||||
| chrX:41142153
|
T | C | 5 | a0001c0001t0001g0134a0001c0001t0001g0146a0001c0001t0001g0149others(2): Show | 5 | NA18939.hp1 NA18946.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+722T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 9/44 | chrX | 41142153 | ||||||
| chrX:41142290
|
A | C | 1 | a0001c0001t0001g0139 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1161+859A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 9/44 | chrX | 41142290 | ||||||
| chrX:41142360
|
G | A | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1161+929G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 9/44 | chrX | 41142360 | ||||||
| chrX:41142368
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1162-923G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 9/44 | chrX | 41142368 | ||||||
| chrX:41142460
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1162-831G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 9/44 | chrX | 41142460 | ||||||
| chrX:41142566
|
G | A | 2 | a0001c0001t0010g0156a0001c0001t0010g0157 | 2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1162-725G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 9/44 | chrX | 41142566 | ||||||
| chrX:41142616
|
C | G | 1 | a0001c0001t0034g0001 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1162-675C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 9/44 | chrX | 41142616 | ||||||
| chrX:41142918
|
TAGAG | T | 57 | a0001c0001t0001g0147a0001c0001t0003g0238a0001c0001t0003g0239others(54): Show | 57 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.1162-370_1162-367d others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 9/44 | INFO_REALIGN_3_PRIME | chrX | 41142918 | |||||
| chrX:41143591
|
T | C | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(133): Show | 136 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1314+148T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 10/44 | chrX | 41143591 | ||||||
| chrX:41143613
|
TA | T | 2 | a0001c0001t0003g0280a0001c0001t0003g0281 | 2 | HG00323.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1314+175delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 10/44 | INFO_REALIGN_3_PRIME | chrX | 41143613 | |||||
| chrX:41143690
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02165.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1314+247A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 10/44 | chrX | 41143690 | ||||||
| chrX:41143760
|
T | C | 3 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145 | 3 | HG01069.hp1 HG01071.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1314+317T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 10/44 | chrX | 41143760 | ||||||
| chrX:41143783
|
C | T | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(132): Show | 135 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1314+340C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 10/44 | chrX | 41143783 | ||||||
| chrX:41143826
|
ATTAT | A | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1314+385_1314+388d others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 10/44 | INFO_REALIGN_3_PRIME | chrX | 41143826 | |||||
| chrX:41143929
|
T | G | 1 | a0001c0001t0005g0063 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1314+486T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 10/44 | chrX | 41143929 | ||||||
| chrX:41143991
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1315-531T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 10/44 | chrX | 41143991 | ||||||
| chrX:41144220
|
A | AT | 205 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1315-285dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 10/44 | INFO_REALIGN_3_PRIME | chrX | 41144220 | |||||
| chrX:41144220
|
A | ATT | 2 | a0001c0001t0001g0173a0002c0005t0011g0236 | 2 | HG06807.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1315-286_1315-285d others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 10/44 | INFO_REALIGN_3_PRIME | chrX | 41144220 | |||||
| chrX:41144220
|
AT | A | 1 | a0001c0001t0003g0280 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1315-285delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 10/44 | INFO_REALIGN_3_PRIME | chrX | 41144220 | |||||
| chrX:41144237
|
T | TG | 1 | a0001c0002t0021g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1315-284dupG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 10/44 | INFO_REALIGN_3_PRIME | chrX | 41144237 | |||||
| chrX:41144237
|
T | TTG | 12 | a0001c0001t0002g0193a0001c0002t0002g0118a0001c0002t0002g0119others(9): Show | 12 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1315-285_1315-284i others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 10/44 | chrX | 41144237 | ||||||
| chrX:41144237
|
T | TTTG | 1 | a0001c0002t0002g0121 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1315-285_1315-284i others(5): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 10/44 | chrX | 41144237 | ||||||
| chrX:41144259
|
G | T | 74 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0131others(71): Show | 74 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1315-263G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 10/44 | chrX | 41144259 | ||||||
| chrX:41144650
|
T | C | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1419+24T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41144650 | ||||||
| chrX:41144948
|
A | C | 1 | a0001c0001t0001g0209 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1419+322A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41144948 | ||||||
| chrX:41144977
|
A | G | 1 | a0001c0002t0002g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1419+351A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41144977 | ||||||
| chrX:41144979
|
G | A | 1 | a0001c0001t0003g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1419+353G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41144979 | ||||||
| chrX:41145490
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0213 | 2 | HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1419+864G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41145490 | ||||||
| chrX:41145536
|
C | G | 4 | a0001c0001t0002g0036a0001c0001t0002g0039a0001c0001t0002g0053others(1): Show | 4 | HG00408.hp1 NA18966.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.1419+910C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41145536 | ||||||
| chrX:41145630
|
C | T | 33 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0134others(30): Show | 33 | HG00738.hp1 HG00741.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.1419+1004C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41145630 | ||||||
| chrX:41146176
|
C | A | 1 | a0001c0001t0004g0272 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1419+1550C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41146176 | ||||||
| chrX:41146197
|
A | G | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1419+1571A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41146197 | ||||||
| chrX:41146300
|
C | T | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(187): Show | 190 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.1419+1674C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41146300 | ||||||
| chrX:41146316
|
A | T | 1 | a0001c0001t0001g0115 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1419+1690A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41146316 | ||||||
| chrX:41146664
|
C | CT | 11 | a0001c0001t0002g0040a0001c0001t0002g0059a0001c0001t0002g0065others(8): Show | 11 | HG00438.hp1 HG00597.hp1 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.1420-1685dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chrX | 41146664 | |||||
| chrX:41146664
|
C | CTT | 45 | a0001c0001t0002g0106a0001c0001t0003g0238a0001c0001t0003g0239others(42): Show | 45 | HG00423.hp1 HG01074.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.1420-1686_1420-168 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chrX | 41146664 | |||||
| chrX:41146664
|
C | CTTT | 10 | a0001c0001t0002g0108a0001c0001t0003g0243a0001c0001t0003g0271others(7): Show | 10 | HG00323.hp1 HG00597.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1420-1687_1420-168 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chrX | 41146664 | |||||
| chrX:41146664
|
C | CTTTT | 1 | a0001c0001t0003g0253 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1420-1688_1420-168 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chrX | 41146664 | |||||
| chrX:41146679
|
TTTTTTG | T | 3 | a0001c0001t0003g0259a0001c0001t0003g0274a0001c0001t0031g0273 | 3 | HG02523.hp1 NA19063.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1420-1689_1420-168 others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41146679 | ||||||
| chrX:41146682
|
TTTG | T | 79 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0129others(76): Show | 79 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1420-1686_1420-168 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41146682 | ||||||
| chrX:41146683
|
TTG | T | 45 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(42): Show | 45 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.1420-1685_1420-168 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41146683 | ||||||
| chrX:41146684
|
TG | T | 15 | a0001c0001t0001g0112a0001c0001t0001g0173a0001c0001t0001g0186others(12): Show | 15 | HG00099.hp1 HG00438.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.1420-1682delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chrX | 41146684 | |||||
| chrX:41146685
|
G | T | 143 | a0001c0001t0002g0011a0001c0001t0002g0013a0001c0001t0002g0015others(140): Show | 143 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.1420-1684G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41146685 | ||||||
| chrX:41146699
|
T | TC | 3 | a0001c0001t0001g0154a0001c0001t0001g0203a0008c0006t0001g0002 | 3 | HG04115.hp1 NA19078.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1420-1663dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chrX | 41146699 | |||||
| chrX:41146775
|
T | C | 292 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1420-1594T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41146775 | ||||||
| chrX:41146787
|
A | G | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1420-1582A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41146787 | ||||||
| chrX:41146854
|
T | C | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1420-1515T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41146854 | ||||||
| chrX:41146971
|
A | C | 1 | a0001c0001t0010g0157 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1420-1398A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41146971 | ||||||
| chrX:41147175
|
G | GT | 1 | a0001c0001t0002g0053 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1420-1180dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chrX | 41147175 | |||||
| chrX:41147175
|
GT | G | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1420-1180delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chrX | 41147175 | |||||
| chrX:41147334
|
C | A | 1 | a0001c0001t0003g0281 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1420-1035C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41147334 | ||||||
| chrX:41147450
|
G | GT | 84 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0115others(81): Show | 84 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1420-899dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chrX | 41147450 | |||||
| chrX:41147450
|
G | GTT | 11 | a0001c0001t0001g0173a0001c0001t0001g0191a0001c0001t0001g0192others(8): Show | 11 | HG01070.hp2 HG02683.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1420-900_1420-899d others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chrX | 41147450 | |||||
| chrX:41147450
|
G | GTTT | 2 | a0001c0001t0001g0194a0001c0001t0008g0103 | 2 | HG01433.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1420-901_1420-899d others(5): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chrX | 41147450 | |||||
| chrX:41147450
|
GT | G | 7 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0048others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1420-899delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chrX | 41147450 | |||||
| chrX:41147450
|
GTT | G | 20 | a0001c0001t0003g0253a0001c0001t0003g0259a0001c0001t0003g0274others(17): Show | 20 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1420-900_1420-899d others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chrX | 41147450 | |||||
| chrX:41147450
|
GTTT | G | 50 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(47): Show | 50 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1420-901_1420-899d others(5): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chrX | 41147450 | |||||
| chrX:41147597
|
G | T | 1 | a0001c0001t0003g0291 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1420-772G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41147597 | ||||||
| chrX:41147681
|
G | C | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(2): Show | 5 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.1420-688G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41147681 | ||||||
| chrX:41147904
|
A | G | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1420-465A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41147904 | ||||||
| chrX:41147916
|
G | A | 3 | a0001c0001t0002g0013a0001c0001t0002g0193a0001c0001t0022g0014 | 3 | HG02615.hp1 HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1420-453G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41147916 | ||||||
| chrX:41147948
|
C | T | 1 | a0001c0001t0005g0066 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1420-421C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41147948 | ||||||
| chrX:41147959
|
G | C | 2 | a0001c0001t0002g0085a0001c0001t0002g0097 | 2 | NA18979.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1420-410G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41147959 | ||||||
| chrX:41147978
|
A | G | 4 | a0001c0001t0002g0024a0001c0001t0002g0041a0001c0001t0002g0042others(1): Show | 4 | HG00642.hp1 HG01081.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-391A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41147978 | ||||||
| chrX:41148061
|
G | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1420-308G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41148061 | ||||||
| chrX:41148172
|
C | T | 3 | a0001c0001t0005g0090a0001c0001t0005g0091a0001c0001t0005g0092 | 3 | HG02148.hp1 NA18973.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1420-197C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41148172 | ||||||
| chrX:41148202
|
T | C | 1 | a0001c0001t0005g0054 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1420-167T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41148202 | ||||||
| chrX:41148323
|
G | A | 1 | a0001c0001t0003g0282 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1420-46G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 11/44 | chrX | 41148323 | ||||||
| chrX:41148687
|
C | T | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1626+112C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 12/44 | chrX | 41148687 | ||||||
| chrX:41148845
|
C | T | 2 | a0001c0001t0010g0156a0001c0001t0010g0157 | 2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1626+270C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 12/44 | chrX | 41148845 | ||||||
| chrX:41149201
|
GTATT | G | 2 | a0001c0001t0002g0193a0001c0002t0002g0174 | 2 | HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1626+631_1626+634d others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 12/44 | INFO_REALIGN_3_PRIME | chrX | 41149201 | |||||
| chrX:41149333
|
T | C | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1626+758T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 12/44 | chrX | 41149333 | ||||||
| chrX:41149385
|
T | C | 1 | a0001c0001t0002g0069 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1626+810T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 12/44 | chrX | 41149385 | ||||||
| chrX:41149400
|
G | T | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1626+825G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 12/44 | chrX | 41149400 | ||||||
| chrX:41149510
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1626+935G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 12/44 | chrX | 41149510 | ||||||
| chrX:41149559
|
T | C | 1 | a0001c0001t0002g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1626+984T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 12/44 | chrX | 41149559 | ||||||
| chrX:41149659
|
C | A | 1 | a0001c0001t0001g0115 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1626+1084C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 12/44 | chrX | 41149659 | ||||||
| chrX:41149710
|
C | CT | 68 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(65): Show | 68 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.1626+1146dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 12/44 | INFO_REALIGN_3_PRIME | chrX | 41149710 | |||||
| chrX:41149765
|
G | A | 74 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0131others(71): Show | 74 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1627-1156G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 12/44 | chrX | 41149765 | ||||||
| chrX:41149820
|
C | T | 31 | a0001c0001t0003g0250a0001c0001t0003g0259a0001c0001t0003g0261others(28): Show | 31 | HG00423.hp1 HG00597.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1627-1101C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 12/44 | chrX | 41149820 | ||||||
| chrX:41150160
|
A | C | 3 | a0001c0001t0005g0012a0001c0001t0005g0063a0001c0001t0005g0064 | 3 | NA18939.hp2 NA18960.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1627-761A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 12/44 | chrX | 41150160 | ||||||
| chrX:41150164
|
C | A | 1 | a0001c0001t0003g0253 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1627-757C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 12/44 | chrX | 41150164 | ||||||
| chrX:41150422
|
C | T | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(191): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.1627-499C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 12/44 | chrX | 41150422 | ||||||
| chrX:41150599
|
C | G | 2 | a0001c0001t0001g0173a0001c0001t0001g0207 | 2 | NA18979.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1627-322C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 12/44 | chrX | 41150599 | ||||||
| chrX:41150783
|
C | A | 14 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(11): Show | 14 | HG00323.hp1 HG02004.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627-138C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 12/44 | chrX | 41150783 | ||||||
| chrX:41150785
|
T | C | 1 | a0001c0001t0002g0108 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1627-136T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 12/44 | chrX | 41150785 | ||||||
| chrX:41150890
|
C | G | 1 | a0001c0001t0001g0201 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1627-31C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 12/44 | chrX | 41150890 | ||||||
| chrX:41151145
|
T | C | 1 | a0001c0002t0002g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1763+88T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | chrX | 41151145 | ||||||
| chrX:41151150
|
A | T | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1763+93A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | chrX | 41151150 | ||||||
| chrX:41151221
|
CT | C | 225 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1763+173delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | INFO_REALIGN_3_PRIME | chrX | 41151221 | |||||
| chrX:41151296
|
C | T | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1763+239C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | chrX | 41151296 | ||||||
| chrX:41151343
|
TGCCAAGA others(9): Show |
T | 1 | a0001c0001t0001g0230 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1763+289_1763+304d others(18): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | INFO_REALIGN_3_PRIME | chrX | 41151343 | |||||
| chrX:41151418
|
G | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1763+361G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | chrX | 41151418 | ||||||
| chrX:41151437
|
T | C | 1 | a0001c0001t0002g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1763+380T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | chrX | 41151437 | ||||||
| chrX:41151442
|
ATTTAT | A | 1 | a0001c0001t0001g0230 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1763+390_1763+394d others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | INFO_REALIGN_3_PRIME | chrX | 41151442 | |||||
| chrX:41151624
|
T | C | 2 | a0001c0001t0002g0193a0001c0002t0002g0174 | 2 | HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1763+567T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | chrX | 41151624 | ||||||
| chrX:41151749
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1763+692G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | chrX | 41151749 | ||||||
| chrX:41152420
|
A | G | 74 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0131others(71): Show | 74 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1764-528A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | chrX | 41152420 | ||||||
| chrX:41152480
|
G | A | 1 | a0001c0002t0002g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1764-468G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | chrX | 41152480 | ||||||
| chrX:41152561
|
G | T | 1 | a0001c0002t0021g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1764-387G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | chrX | 41152561 | ||||||
| chrX:41152624
|
CT | C | 1 | a0001c0001t0001g0131 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1764-323delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | chrX | 41152624 | ||||||
| chrX:41152631
|
A | G | 1 | a0001c0001t0024g0234 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1764-317A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | chrX | 41152631 | ||||||
| chrX:41152673
|
G | A | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1764-275G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | chrX | 41152673 | ||||||
| chrX:41152777
|
T | C | 1 | a0001c0001t0008g0135 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1764-171T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | chrX | 41152777 | ||||||
| chrX:41152778
|
CT | C | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1764-166delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | INFO_REALIGN_3_PRIME | chrX | 41152778 | |||||
| chrX:41152849
|
G | T | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1764-99G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | chrX | 41152849 | ||||||
| chrX:41152898
|
A | G | 8 | a0001c0002t0002g0118a0001c0002t0002g0119a0001c0002t0002g0120others(5): Show | 8 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1764-50A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | chrX | 41152898 | ||||||
| chrX:41152929
|
T | C | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1764-19T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 13/44 | chrX | 41152929 | ||||||
| chrX:41153109
|
T | C | 1 | a0001c0001t0003g0286 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1897+28T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41153109 | ||||||
| chrX:41153193
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1897+112C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41153193 | ||||||
| chrX:41153225
|
C | G | 1 | a0001c0002t0002g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1897+144C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41153225 | ||||||
| chrX:41153233
|
TAA | T | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(130): Show | 133 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1897+153_1897+154d others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41153233 | ||||||
| chrX:41153361
|
A | C | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1897+280A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41153361 | ||||||
| chrX:41153380
|
T | C | 7 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(4): Show | 7 | HG01891.hp1 HG02895.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1897+299T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41153380 | ||||||
| chrX:41153421
|
T | G | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1897+340T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41153421 | ||||||
| chrX:41153466
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1897+385A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41153466 | ||||||
| chrX:41153880
|
C | A | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1897+799C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41153880 | ||||||
| chrX:41154130
|
T | C | 14 | a0001c0001t0002g0193a0001c0002t0002g0118a0001c0002t0002g0119others(11): Show | 14 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1897+1049T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41154130 | ||||||
| chrX:41154196
|
G | C | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.1897+1115G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41154196 | ||||||
| chrX:41154453
|
C | T | 279 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(276): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1897+1372C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41154453 | ||||||
| chrX:41154502
|
T | C | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1897+1421T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41154502 | ||||||
| chrX:41154634
|
C | T | 1 | a0001c0001t0007g0020 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1897+1553C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41154634 | ||||||
| chrX:41154784
|
T | C | 1 | a0001c0001t0002g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1897+1703T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41154784 | ||||||
| chrX:41154854
|
C | T | 5 | a0001c0001t0002g0033a0001c0001t0002g0049a0001c0001t0002g0086others(2): Show | 5 | HG01258.hp1 HG01261.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.1897+1773C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41154854 | ||||||
| chrX:41154938
|
T | C | 14 | a0001c0001t0002g0193a0001c0002t0002g0118a0001c0002t0002g0119others(11): Show | 14 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1897+1857T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41154938 | ||||||
| chrX:41155503
|
C | T | 2 | a0001c0002t0002g0119a0001c0002t0002g0120 | 2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1897+2422C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41155503 | ||||||
| chrX:41155627
|
T | A | 1 | a0001c0001t0001g0203 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1897+2546T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41155627 | ||||||
| chrX:41155704
|
T | TA | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1897+2623_1897+262 others(5): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41155704 | ||||||
| chrX:41155808
|
C | T | 1 | a0001c0001t0005g0051 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1897+2727C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41155808 | ||||||
| chrX:41155830
|
A | T | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1897+2749A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41155830 | ||||||
| chrX:41155877
|
A | C | 1 | a0001c0001t0002g0013 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1897+2796A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41155877 | ||||||
| chrX:41156087
|
G | C | 1 | a0001c0001t0002g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1897+3006G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41156087 | ||||||
| chrX:41156603
|
A | G | 197 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1897+3522A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41156603 | ||||||
| chrX:41156725
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1897+3644G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41156725 | ||||||
| chrX:41156728
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1897+3647C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41156728 | ||||||
| chrX:41156759
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1897+3678G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41156759 | ||||||
| chrX:41157049
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1897+3968C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41157049 | ||||||
| chrX:41157086
|
A | G | 1 | a0001c0001t0031g0273 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1897+4005A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41157086 | ||||||
| chrX:41157157
|
G | C | 1 | a0001c0002t0021g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1897+4076G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41157157 | ||||||
| chrX:41157247
|
C | G | 86 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0131others(83): Show | 86 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1897+4166C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41157247 | ||||||
| chrX:41157367
|
T | G | 86 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0131others(83): Show | 86 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1897+4286T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41157367 | ||||||
| chrX:41157841
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1897+4760C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41157841 | ||||||
| chrX:41157852
|
A | G | 1 | a0001c0002t0002g0215 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1897+4771A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41157852 | ||||||
| chrX:41157926
|
T | TA | 1 | a0001c0001t0008g0136 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1897+4848dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41157926 | |||||
| chrX:41158529
|
TAAAC | T | 9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 9 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1898-4257_1898-425 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41158529 | |||||
| chrX:41158730
|
T | TG | 1 | a0001c0001t0004g0265 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1898-4054dupG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41158730 | |||||
| chrX:41158751
|
C | T | 1 | a0001c0001t0005g0067 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1898-4039C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41158751 | ||||||
| chrX:41158985
|
T | C | 1 | a0001c0008t0002g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1898-3805T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41158985 | ||||||
| chrX:41159043
|
CTCCAACC others(18): Show |
C | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0006g0008 | 3 | NA18981.hp1 NA18984.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1898-3746_1898-372 others(29): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41159043 | ||||||
| chrX:41159199
|
G | A | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1898-3591G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41159199 | ||||||
| chrX:41159243
|
A | C | 1 | a0001c0001t0005g0066 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1898-3547A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41159243 | ||||||
| chrX:41159525
|
C | CT | 4 | a0001c0001t0003g0288a0001c0001t0013g0180a0001c0001t0028g0179others(1): Show | 4 | HG02559.hp1 HG03195.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1898-3253dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41159525 | |||||
| chrX:41159525
|
CT | C | 5 | a0001c0001t0002g0019a0001c0001t0002g0040a0001c0001t0009g0025others(2): Show | 5 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1898-3253delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41159525 | |||||
| chrX:41159538
|
C | CT | 1 | a0001c0001t0027g0104 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1898-3243dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41159538 | |||||
| chrX:41159610
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1898-3180A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41159610 | ||||||
| chrX:41159963
|
AAATTG | A | 1 | a0001c0001t0001g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1898-2821_1898-281 others(9): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41159963 | |||||
| chrX:41160014
|
G | GT | 1 | a0001c0001t0002g0046 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1898-2766dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41160014 | |||||
| chrX:41160036
|
T | TA | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1898-2750dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41160036 | |||||
| chrX:41160164
|
C | G | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.1898-2626C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41160164 | ||||||
| chrX:41160283
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0114 | 3 | NA18951.hp1 NA18994.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1898-2507C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41160283 | ||||||
| chrX:41160321
|
CAT | C | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1898-2455_1898-245 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41160321 | |||||
| chrX:41160362
|
T | C | 8 | a0001c0002t0002g0118a0001c0002t0002g0119a0001c0002t0002g0120others(5): Show | 8 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1898-2428T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41160362 | ||||||
| chrX:41160702
|
C | T | 1 | a0001c0001t0002g0037 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1898-2088C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41160702 | ||||||
| chrX:41160906
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1898-1884A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41160906 | ||||||
| chrX:41161000
|
T | G | 1 | a0001c0001t0030g0275 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1898-1790T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41161000 | ||||||
| chrX:41161087
|
G | A | 279 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(276): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1898-1703G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41161087 | ||||||
| chrX:41161174
|
G | A | 2 | a0001c0001t0013g0180a0001c0001t0028g0179 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1898-1616G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41161174 | ||||||
| chrX:41161329
|
C | CT | 45 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0109others(42): Show | 45 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1898-1434dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161329 | |||||
| chrX:41161329
|
C | CTT | 9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 9 | HG01167.hp1 HG02895.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1898-1435_1898-143 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161329 | |||||
| chrX:41161329
|
C | CTTT | 47 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0131others(44): Show | 47 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.1898-1436_1898-143 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161329 | |||||
| chrX:41161329
|
C | CTTTT | 27 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0001t0001g0139others(24): Show | 27 | HG00673.hp1 HG00738.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.1898-1437_1898-143 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161329 | |||||
| chrX:41161329
|
C | CTTTTT | 7 | a0001c0001t0001g0140a0001c0001t0001g0204a0001c0001t0010g0156others(4): Show | 7 | HG00741.hp1 HG02135.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1898-1438_1898-143 others(9): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161329 | |||||
| chrX:41161329
|
C | CTTTTTT | 1 | a0001c0001t0001g0208 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1898-1439_1898-143 others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161329 | |||||
| chrX:41161329
|
C | CTTTTTTT | 2 | a0001c0002t0002g0121a0001c0002t0002g0215 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1898-1440_1898-143 others(11): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161329 | |||||
| chrX:41161329
|
C | CTTTTTTT others(1): Show |
4 | a0001c0002t0002g0118a0001c0002t0002g0122a0001c0002t0002g0176others(1): Show | 4 | HG01891.hp2 HG02258.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1898-1441_1898-143 others(12): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161329 | |||||
| chrX:41161329
|
C | CTTTTTTT others(3): Show |
1 | a0001c0002t0021g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1898-1443_1898-143 others(14): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161329 | |||||
| chrX:41161329
|
C | CTTTTTTT others(4): Show |
1 | a0001c0008t0002g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1898-1444_1898-143 others(15): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161329 | |||||
| chrX:41161329
|
CT | C | 2 | a0001c0001t0001g0188a0001c0001t0009g0061 | 2 | HG00735.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1898-1434delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161329 | |||||
| chrX:41161329
|
CTT | C | 7 | a0001c0001t0003g0253a0001c0001t0003g0267a0001c0001t0003g0276others(4): Show | 7 | HG00423.hp1 HG02071.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1898-1435_1898-143 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161329 | |||||
| chrX:41161329
|
CTTT | C | 45 | a0001c0001t0003g0239a0001c0001t0003g0241a0001c0001t0003g0250others(42): Show | 45 | HG00323.hp1 HG00597.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.1898-1436_1898-143 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161329 | |||||
| chrX:41161329
|
CTTTT | C | 4 | a0001c0001t0003g0238a0001c0001t0003g0243a0001c0001t0003g0244others(1): Show | 4 | HG01243.hp1 HG02145.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1898-1437_1898-143 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161329 | |||||
| chrX:41161329
|
CTTTTTT | C | 1 | a0001c0001t0002g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1898-1439_1898-143 others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161329 | |||||
| chrX:41161329
|
CTTTTTTT | C | 1 | a0001c0002t0002g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1898-1440_1898-143 others(11): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161329 | |||||
| chrX:41161329
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1898-1445_1898-143 others(16): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161329 | |||||
| chrX:41161362
|
C | T | 1 | a0001c0001t0003g0292 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1898-1428C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41161362 | ||||||
| chrX:41161635
|
C | CT | 6 | a0001c0001t0001g0007a0001c0001t0002g0024a0001c0001t0002g0060others(3): Show | 6 | HG00621.hp1 HG00642.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1898-1132dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTT | 13 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(10): Show | 13 | HG00099.hp2 HG00408.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1898-1133_1898-113 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTT | 4 | a0001c0002t0002g0196a0001c0002t0002g0215a0001c0002t0021g0195others(1): Show | 4 | HG03486.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1898-1134_1898-113 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTT | 9 | a0001c0001t0001g0190a0001c0001t0002g0193a0001c0002t0002g0118others(6): Show | 9 | HG00733.hp1 HG01891.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1898-1135_1898-113 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTT | 6 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0229others(3): Show | 6 | HG02056.hp1 HG02135.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1898-1136_1898-113 others(9): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTT | 5 | a0001c0001t0001g0164a0001c0001t0001g0182a0001c0001t0001g0183others(2): Show | 5 | HG00140.hp1 HG00609.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1898-1137_1898-113 others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT | 4 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1898-1138_1898-113 others(11): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(1): Show |
2 | a0001c0001t0001g0162a0001c0001t0024g0234 | 2 | HG00558.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1898-1139_1898-113 others(12): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(2): Show |
1 | a0001c0001t0001g0111 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1898-1140_1898-113 others(13): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(4): Show |
8 | a0001c0001t0001g0158a0001c0001t0001g0170a0001c0001t0003g0263others(5): Show | 8 | HG00597.hp2 HG02155.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.1898-1142_1898-113 others(15): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(5): Show |
20 | a0001c0001t0001g0161a0001c0001t0001g0169a0001c0001t0003g0239others(17): Show | 20 | HG00423.hp1 HG00423.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1898-1143_1898-113 others(16): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(6): Show |
19 | a0001c0001t0003g0238a0001c0001t0003g0244a0001c0001t0003g0269others(16): Show | 19 | HG00323.hp1 HG01074.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1898-1144_1898-113 others(17): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(7): Show |
13 | a0001c0001t0001g0144a0001c0001t0003g0243a0001c0001t0003g0253others(10): Show | 13 | HG01099.hp1 HG01175.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.1898-1145_1898-113 others(18): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0001g0187a0001c0001t0031g0273 | 2 | HG00558.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1898-1146_1898-113 others(19): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(9): Show |
3 | a0001c0001t0001g0223a0001c0001t0001g0228a0001c0001t0032g0222 | 3 | HG02895.hp1 HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1898-1147_1898-113 others(20): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0001g0207 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1898-1148_1898-113 others(21): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(11): Show |
2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1898-1149_1898-113 others(22): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(12): Show |
3 | a0001c0001t0001g0139a0001c0001t0001g0224a0001c0001t0001g0227 | 3 | HG02976.hp2 HG03942.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1898-1150_1898-113 others(23): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0001g0230 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1898-1151_1898-113 others(24): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(14): Show |
1 | a0001c0001t0001g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1898-1152_1898-113 others(25): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(15): Show |
10 | a0001c0001t0001g0010a0001c0001t0001g0113a0001c0001t0001g0131others(7): Show | 10 | HG01081.hp1 HG01943.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.1898-1153_1898-113 others(26): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(16): Show |
3 | a0001c0001t0001g0132a0001c0001t0001g0197a0001c0001t0001g0208 | 3 | HG02148.hp2 HG02293.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1898-1154_1898-113 others(27): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(18): Show |
2 | a0001c0001t0001g0214a0001c0001t0006g0008 | 2 | NA18967.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1898-1132_1898-113 others(29): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0001g0218 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1898-1132_1898-113 others(30): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(20): Show |
4 | a0001c0001t0001g0006a0001c0001t0001g0138a0001c0001t0001g0213others(1): Show | 4 | HG03486.hp2 HG03491.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1898-1132_1898-113 others(31): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(21): Show |
5 | a0001c0001t0001g0009a0001c0001t0001g0109a0001c0001t0001g0192others(2): Show | 5 | HG02155.hp1 HG02165.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.1898-1132_1898-113 others(32): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(22): Show |
2 | a0001c0001t0001g0112a0001c0001t0001g0114 | 2 | HG00438.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1898-1132_1898-113 others(33): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(25): Show |
1 | a0001c0001t0001g0191 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1898-1132_1898-113 others(36): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(28): Show |
1 | a0001c0001t0001g0004 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1898-1132_1898-113 others(39): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(29): Show |
2 | a0001c0001t0001g0003a0001c0001t0001g0188 | 2 | HG03831.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1898-1132_1898-113 others(40): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(31): Show |
1 | a0001c0001t0003g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1898-1132_1898-113 others(42): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(34): Show |
1 | a0001c0001t0001g0173 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1898-1132_1898-113 others(45): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
C | CTTTTTTT others(40): Show |
2 | a0001c0001t0001g0110a0001c0001t0001g0217 | 2 | HG00673.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1898-1132_1898-113 others(51): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
CTT | C | 4 | a0001c0001t0002g0210a0001c0004t0002g0177a0001c0004t0002g0178others(1): Show | 4 | HG02615.hp2 HG02723.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1898-1133_1898-113 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
CTTT | C | 3 | a0002c0005t0011g0235a0002c0005t0011g0236a0007c0012t0001g0105 | 3 | HG03453.hp1 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1898-1134_1898-113 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
CTTTT | C | 32 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0134others(29): Show | 32 | HG00738.hp1 HG00741.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.1898-1135_1898-113 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161635
|
CTTTTT | C | 1 | a0001c0001t0001g0206 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1898-1136_1898-113 others(9): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161635 | |||||
| chrX:41161755
|
C | CT | 1 | a0001c0001t0002g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1898-1023dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chrX | 41161755 | |||||
| chrX:41161814
|
C | T | 1 | a0001c0001t0009g0061 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1898-976C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41161814 | ||||||
| chrX:41161995
|
A | G | 197 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1898-795A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41161995 | ||||||
| chrX:41162025
|
C | T | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1898-765C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41162025 | ||||||
| chrX:41162121
|
G | C | 4 | a0001c0001t0003g0263a0001c0001t0003g0267a0001c0001t0003g0269others(1): Show | 4 | NA18950.hp2 NA19066.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.1898-669G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41162121 | ||||||
| chrX:41162292
|
G | C | 1 | a0001c0001t0002g0069 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1898-498G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 14/44 | chrX | 41162292 | ||||||
| chrX:41163211
|
A | T | 13 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(10): Show | 13 | HG00438.hp2 HG02074.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.1985+334A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41163211 | ||||||
| chrX:41163403
|
C | T | 1 | a0001c0001t0030g0275 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1985+526C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41163403 | ||||||
| chrX:41163432
|
TA | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1985+557delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chrX | 41163432 | |||||
| chrX:41163435
|
C | G | 1 | a0001c0001t0033g0240 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1985+558C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41163435 | ||||||
| chrX:41163444
|
A | G | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1985+567A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41163444 | ||||||
| chrX:41163447
|
G | C | 1 | a0001c0008t0002g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1985+570G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41163447 | ||||||
| chrX:41163481
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1985+604G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41163481 | ||||||
| chrX:41163678
|
C | T | 3 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0032g0222 | 3 | HG01891.hp1 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1985+801C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41163678 | ||||||
| chrX:41163734
|
CA | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0189 | 2 | HG02809.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1985+873delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chrX | 41163734 | |||||
| chrX:41163734
|
CAAAA | C | 1 | a0001c0001t0001g0187 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1985+870_1985+873d others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chrX | 41163734 | |||||
| chrX:41163750
|
A | T | 1 | a0001c0001t0027g0104 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1985+873A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41163750 | ||||||
| chrX:41163983
|
C | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1985+1106C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41163983 | ||||||
| chrX:41164021
|
C | T | 1 | a0001c0001t0003g0292 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1985+1144C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41164021 | ||||||
| chrX:41164118
|
G | A | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG00438.hp2 HG02155.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.1985+1241G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41164118 | ||||||
| chrX:41164118
|
G | C | 2 | a0001c0001t0003g0269a0001c0001t0003g0271 | 2 | NA19066.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1985+1241G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41164118 | ||||||
| chrX:41164205
|
T | C | 2 | a0001c0001t0002g0041a0001c0001t0002g0042 | 2 | HG01255.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1985+1328T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41164205 | ||||||
| chrX:41164346
|
GT | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1985+1480delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chrX | 41164346 | |||||
| chrX:41164348
|
T | G | 1 | a0001c0001t0001g0134 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1985+1471T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41164348 | ||||||
| chrX:41164651
|
T | C | 1 | a0001c0001t0002g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1986-1221T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41164651 | ||||||
| chrX:41164750
|
T | C | 33 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0134others(30): Show | 33 | HG00738.hp1 HG00741.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.1986-1122T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41164750 | ||||||
| chrX:41164827
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0232 | 2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1986-1045G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41164827 | ||||||
| chrX:41164911
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1986-961C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41164911 | ||||||
| chrX:41164986
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1986-886T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41164986 | ||||||
| chrX:41165057
|
G | T | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1986-815G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41165057 | ||||||
| chrX:41165171
|
GGTT | G | 120 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1986-690_1986-688d others(5): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chrX | 41165171 | |||||
| chrX:41165174
|
T | G | 4 | a0001c0001t0002g0037a0001c0001t0002g0038a0001c0001t0002g0059others(1): Show | 4 | NA18940.hp1 NA18945.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1986-698T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41165174 | ||||||
| chrX:41165179
|
T | C | 1 | a0001c0008t0002g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1986-693T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41165179 | ||||||
| chrX:41165852
|
A | G | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1986-20A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 15/44 | chrX | 41165852 | ||||||
| chrX:41166713
|
C | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.2328+499C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 16/44 | chrX | 41166713 | ||||||
| chrX:41166774
|
C | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.2328+560C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 16/44 | chrX | 41166774 | ||||||
| chrX:41166811
|
G | A | 1 | a0001c0001t0004g0255 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2328+597G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 16/44 | chrX | 41166811 | ||||||
| chrX:41167388
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2329-94T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 16/44 | chrX | 41167388 | ||||||
| chrX:41167433
|
C | A | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2329-49C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 16/44 | chrX | 41167433 | ||||||
| chrX:41167718
|
T | C | 3 | a0001c0001t0004g0260a0001c0001t0004g0268a0001c0001t0004g0277 | 3 | NA18990.hp1 NA19009.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2424+141T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 17/44 | chrX | 41167718 | ||||||
| chrX:41167912
|
A | G | 1 | a0001c0001t0001g0206 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2425-95A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 17/44 | chrX | 41167912 | ||||||
| chrX:41168561
|
C | T | 3 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145 | 3 | HG01069.hp1 HG01071.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2636+343C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 18/44 | chrX | 41168561 | ||||||
| chrX:41168649
|
C | A | 1 | a0001c0001t0004g0270 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2636+431C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 18/44 | chrX | 41168649 | ||||||
| chrX:41168831
|
A | G | 13 | a0001c0002t0002g0118a0001c0002t0002g0119a0001c0002t0002g0120others(10): Show | 13 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.2636+613A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 18/44 | chrX | 41168831 | ||||||
| chrX:41168870
|
G | A | 1 | a0001c0001t0003g0287 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2636+652G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 18/44 | chrX | 41168870 | ||||||
| chrX:41168876
|
T | C | 1 | a0001c0001t0002g0079 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2636+658T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 18/44 | chrX | 41168876 | ||||||
| chrX:41168892
|
A | AT | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2636+682dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 18/44 | INFO_REALIGN_3_PRIME | chrX | 41168892 | |||||
| chrX:41169120
|
G | GT | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2637-874dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 18/44 | INFO_REALIGN_3_PRIME | chrX | 41169120 | |||||
| chrX:41169144
|
A | AT | 2 | a0001c0001t0013g0180a0001c0001t0028g0179 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2637-840dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 18/44 | INFO_REALIGN_3_PRIME | chrX | 41169144 | |||||
| chrX:41169488
|
C | T | 59 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0003g0238others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2637-507C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 18/44 | chrX | 41169488 | ||||||
| chrX:41169599
|
C | T | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2637-396C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 18/44 | chrX | 41169599 | ||||||
| chrX:41169707
|
C | T | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2637-288C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 18/44 | chrX | 41169707 | ||||||
| chrX:41169729
|
T | TA | 1 | a0001c0001t0003g0282 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2637-265dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 18/44 | INFO_REALIGN_3_PRIME | chrX | 41169729 | |||||
| chrX:41170342
|
G | A | 6 | a0001c0001t0003g0250a0001c0001t0003g0261a0001c0001t0003g0263others(3): Show | 6 | NA18747.hp1 NA18950.hp2 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.2877+107G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 19/44 | chrX | 41170342 | ||||||
| chrX:41170380
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2878-90C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 19/44 | chrX | 41170380 | ||||||
| chrX:41170668
|
GT | G | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.3027+54delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 20/44 | INFO_REALIGN_3_PRIME | chrX | 41170668 | |||||
| chrX:41170703
|
T | G | 1 | a0001c0002t0002g0119 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3027+84T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 20/44 | chrX | 41170703 | ||||||
| chrX:41171065
|
TG | T | 1 | a0001c0008t0002g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3027+449delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 20/44 | INFO_REALIGN_3_PRIME | chrX | 41171065 | |||||
| chrX:41171069
|
A | G | 1 | a0001c0001t0005g0066 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3027+450A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 20/44 | chrX | 41171069 | ||||||
| chrX:41171076
|
T | G | 1 | a0001c0008t0002g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3027+457T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 20/44 | chrX | 41171076 | ||||||
| chrX:41171081
|
A | G | 4 | a0001c0001t0002g0210a0001c0004t0002g0177a0001c0004t0002g0178others(1): Show | 4 | HG02615.hp2 HG02723.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3027+462A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 20/44 | chrX | 41171081 | ||||||
| chrX:41171125
|
C | T | 1 | a0001c0001t0005g0090 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3027+506C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 20/44 | chrX | 41171125 | ||||||
| chrX:41171216
|
TC | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.3027+599delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 20/44 | INFO_REALIGN_3_PRIME | chrX | 41171216 | |||||
| chrX:41171395
|
G | A | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3028-443G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 20/44 | chrX | 41171395 | ||||||
| chrX:41171649
|
TTGA | T | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3028-183_3028-181d others(5): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 20/44 | INFO_REALIGN_3_PRIME | chrX | 41171649 | |||||
| chrX:41171650
|
T | A | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.3028-188T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 20/44 | chrX | 41171650 | ||||||
| chrX:41171662
|
T | G | 1 | a0001c0001t0002g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3028-176T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 20/44 | chrX | 41171662 | ||||||
| chrX:41172148
|
CA | C | 1 | a0001c0001t0019g0018 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3148+200delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41172148 | |||||
| chrX:41172166
|
G | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3148+208G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41172166 | ||||||
| chrX:41172558
|
A | G | 2 | a0001c0001t0013g0180a0001c0001t0028g0179 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3148+600A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41172558 | ||||||
| chrX:41172590
|
G | A | 1 | a0001c0001t0008g0136 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3148+632G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41172590 | ||||||
| chrX:41172773
|
A | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3148+815A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41172773 | ||||||
| chrX:41173418
|
A | ACCTAAAA others(880): Show |
1 | a0001c0001t0001g0229 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3148+1474_3148+147 others(891): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41173418 | |||||
| chrX:41173630
|
A | G | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3148+1672A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41173630 | ||||||
| chrX:41173675
|
A | G | 1 | a0001c0001t0006g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3148+1717A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41173675 | ||||||
| chrX:41173678
|
A | G | 1 | a0001c0001t0006g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3148+1720A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41173678 | ||||||
| chrX:41173684
|
T | C | 1 | a0001c0001t0006g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3148+1726T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41173684 | ||||||
| chrX:41173786
|
G | C | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3148+1828G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41173786 | ||||||
| chrX:41173986
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3148+2028G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41173986 | ||||||
| chrX:41173997
|
A | C | 7 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(4): Show | 7 | HG01891.hp1 HG02895.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.3148+2039A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41173997 | ||||||
| chrX:41174215
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0025g0133 | 2 | HG03654.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.3148+2257C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41174215 | ||||||
| chrX:41174362
|
C | G | 8 | a0001c0002t0002g0118a0001c0002t0002g0119a0001c0002t0002g0120others(5): Show | 8 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.3148+2404C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41174362 | ||||||
| chrX:41174365
|
T | C | 2 | a0001c0001t0008g0103a0001c0001t0008g0142 | 2 | HG01070.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.3148+2407T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41174365 | ||||||
| chrX:41174492
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3148+2534T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41174492 | ||||||
| chrX:41174504
|
C | T | 1 | a0001c0001t0003g0283 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3148+2546C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41174504 | ||||||
| chrX:41174552
|
G | T | 7 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(4): Show | 7 | HG01891.hp1 HG02895.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.3148+2594G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41174552 | ||||||
| chrX:41175392
|
G | A | 2 | a0001c0001t0002g0078a0001c0001t0002g0088 | 2 | NA18951.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.3148+3434G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41175392 | ||||||
| chrX:41175436
|
A | T | 1 | a0001c0001t0019g0018 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3148+3478A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41175436 | ||||||
| chrX:41175522
|
CA | C | 2 | a0001c0001t0002g0019a0001c0001t0003g0280 | 2 | HG00323.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.3148+3577delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41175522 | |||||
| chrX:41175675
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3148+3717A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41175675 | ||||||
| chrX:41175772
|
T | TACACACA others(3): Show |
2 | a0001c0001t0003g0274a0001c0001t0003g0287 | 2 | HG02683.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.3148+3818_3148+382 others(14): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41175772 | |||||
| chrX:41175772
|
T | TACACACA others(5): Show |
48 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(45): Show | 48 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3148+3816_3148+382 others(16): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41175772 | |||||
| chrX:41175772
|
T | TACACACA others(7): Show |
5 | a0001c0001t0003g0263a0001c0001t0003g0267a0001c0001t0003g0269others(2): Show | 5 | NA18950.hp2 NA18968.hp2 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.3148+3827_3148+382 others(18): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41175772 | |||||
| chrX:41175784
|
C | CACACACA others(5): Show |
1 | a0001c0001t0003g0282 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3148+3827_3148+382 others(16): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41175784 | |||||
| chrX:41175806
|
A | T | 189 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.3148+3848A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41175806 | ||||||
| chrX:41175837
|
TCCTC | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3148+3882_3148+388 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41175837 | |||||
| chrX:41175895
|
A | AT | 7 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0184others(4): Show | 7 | HG00735.hp1 HG00735.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.3148+3951dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41175895 | |||||
| chrX:41175895
|
AT | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0110a0002c0005t0011g0235others(1): Show | 4 | HG06807.hp1 NA18962.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.3148+3951delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41175895 | |||||
| chrX:41176423
|
A | AGT | 1 | a0001c0001t0003g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3148+4466_3148+446 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41176423 | |||||
| chrX:41176939
|
A | T | 5 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0048others(2): Show | 5 | HG02451.hp2 HG02723.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.3148+4981A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41176939 | ||||||
| chrX:41177317
|
C | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3148+5359C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41177317 | ||||||
| chrX:41177578
|
A | G | 1 | a0001c0001t0008g0136 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3148+5620A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41177578 | ||||||
| chrX:41177755
|
A | G | 17 | a0001c0001t0004g0242a0001c0001t0004g0245a0001c0001t0004g0248others(14): Show | 17 | HG00423.hp1 HG00597.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.3148+5797A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41177755 | ||||||
| chrX:41178027
|
C | T | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3149-5971C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41178027 | ||||||
| chrX:41178084
|
C | CT | 33 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0227others(30): Show | 33 | HG00642.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.3149-5884dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41178084 | |||||
| chrX:41178084
|
C | CTT | 8 | a0001c0001t0002g0042a0001c0001t0003g0253a0001c0001t0003g0276others(5): Show | 8 | HG01255.hp1 HG02148.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.3149-5885_3149-588 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41178084 | |||||
| chrX:41178084
|
C | CTTT | 2 | a0001c0001t0003g0243a0006c0007t0020g0098 | 2 | HG02145.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.3149-5886_3149-588 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41178084 | |||||
| chrX:41178084
|
C | CTTTT | 2 | a0001c0001t0003g0238a0001c0001t0003g0244 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3149-5887_3149-588 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41178084 | |||||
| chrX:41178084
|
CT | C | 100 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0110others(97): Show | 100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.3149-5884delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41178084 | |||||
| chrX:41178084
|
CTT | C | 27 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0001g0129others(24): Show | 27 | HG00738.hp1 HG01168.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.3149-5885_3149-588 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41178084 | |||||
| chrX:41178084
|
CTTT | C | 3 | a0001c0001t0001g0134a0001c0001t0008g0142a0001c0003t0001g0130 | 3 | HG01070.hp2 NA18939.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.3149-5886_3149-588 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41178084 | |||||
| chrX:41178084
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | NA18951.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.3149-5895_3149-588 others(16): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41178084 | |||||
| chrX:41178253
|
C | A | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.3149-5745C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41178253 | ||||||
| chrX:41178478
|
A | G | 11 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0036others(8): Show | 11 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.3149-5520A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41178478 | ||||||
| chrX:41178718
|
A | G | 2 | a0001c0001t0008g0103a0001c0001t0008g0142 | 2 | HG01070.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.3149-5280A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41178718 | ||||||
| chrX:41178742
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3149-5256T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41178742 | ||||||
| chrX:41179067
|
ATCTG | A | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3149-4929_3149-492 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41179067 | |||||
| chrX:41179200
|
T | G | 1 | a0001c0001t0001g0129 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3149-4798T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41179200 | ||||||
| chrX:41179236
|
A | AT | 13 | a0001c0001t0002g0193a0001c0002t0002g0118a0001c0002t0002g0119others(10): Show | 13 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.3149-4755dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41179236 | |||||
| chrX:41179921
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3149-4077G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41179921 | ||||||
| chrX:41180365
|
T | G | 1 | a0001c0001t0002g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3149-3633T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41180365 | ||||||
| chrX:41180525
|
G | A | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.3149-3473G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41180525 | ||||||
| chrX:41180558
|
A | AT | 1 | a0001c0001t0001g0126 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3149-3440_3149-343 others(5): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41180558 | ||||||
| chrX:41180830
|
A | G | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.3149-3168A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41180830 | ||||||
| chrX:41180931
|
A | T | 2 | a0001c0001t0002g0106a0001c0001t0012g0107 | 2 | HG01496.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.3149-3067A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41180931 | ||||||
| chrX:41181272
|
C | CT | 71 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0131others(68): Show | 71 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.3149-2705dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41181272 | |||||
| chrX:41181272
|
C | CTT | 2 | a0001c0001t0001g0203a0001c0001t0004g0242 | 2 | HG01074.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.3149-2706_3149-270 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41181272 | |||||
| chrX:41181272
|
C | CTTT | 50 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(47): Show | 50 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.3149-2707_3149-270 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41181272 | |||||
| chrX:41181272
|
C | CTTTT | 5 | a0001c0001t0003g0243a0001c0001t0003g0264a0001c0001t0004g0260others(2): Show | 5 | HG01358.hp1 HG02145.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.3149-2708_3149-270 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41181272 | |||||
| chrX:41181272
|
CT | C | 16 | a0001c0001t0001g0110a0001c0001t0002g0013a0001c0001t0002g0019others(13): Show | 16 | HG00323.hp2 HG00642.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.3149-2705delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41181272 | |||||
| chrX:41181276
|
T | C | 1 | a0001c0001t0002g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3149-2722T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41181276 | ||||||
| chrX:41181293
|
T | TA | 1 | a0001c0001t0002g0072 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.3149-2702dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41181293 | |||||
| chrX:41181435
|
C | CT | 45 | a0001c0001t0001g0007a0001c0001t0001g0110a0001c0001t0001g0190others(42): Show | 45 | HG00642.hp1 HG00733.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.3149-2534dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41181435 | |||||
| chrX:41181435
|
C | CTT | 33 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.3149-2535_3149-253 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41181435 | |||||
| chrX:41181435
|
C | CTTT | 43 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0115others(40): Show | 43 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.3149-2536_3149-253 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41181435 | |||||
| chrX:41181435
|
C | CTTTT | 31 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0001g0152others(28): Show | 31 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.3149-2537_3149-253 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41181435 | |||||
| chrX:41181435
|
C | CTTTTT | 8 | a0001c0001t0001g0129a0001c0001t0001g0202a0001c0001t0001g0203others(5): Show | 8 | HG02040.hp1 HG02622.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.3149-2538_3149-253 others(9): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41181435 | |||||
| chrX:41181435
|
C | CTTTTTT | 3 | a0001c0001t0001g0139a0001c0001t0001g0158a0001c0001t0001g0204 | 3 | HG02135.hp1 HG03942.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.3149-2539_3149-253 others(10): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41181435 | |||||
| chrX:41181435
|
CT | C | 6 | a0001c0001t0002g0011a0001c0001t0002g0016a0001c0001t0002g0049others(3): Show | 6 | HG01168.hp1 HG02165.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.3149-2534delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41181435 | |||||
| chrX:41181435
|
CTTTTTTT others(2): Show |
C | 1 | a0001c0002t0002g0121 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3149-2542_3149-253 others(13): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41181435 | |||||
| chrX:41181435
|
CTTTTTTT others(8): Show |
C | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3149-2548_3149-253 others(19): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41181435 | |||||
| chrX:41181435
|
CTTTTTTT others(16): Show |
C | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3149-2556_3149-253 others(27): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41181435 | |||||
| chrX:41181510
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3149-2488G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41181510 | ||||||
| chrX:41181722
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02155.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.3149-2276T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41181722 | ||||||
| chrX:41181820
|
C | T | 1 | a0001c0001t0006g0008 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3149-2178C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41181820 | ||||||
| chrX:41181982
|
A | G | 197 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.3149-2016A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41181982 | ||||||
| chrX:41182014
|
A | C | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3149-1984A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41182014 | ||||||
| chrX:41182108
|
C | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3149-1890C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41182108 | ||||||
| chrX:41182376
|
G | GA | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG00099.hp2 HG01123.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.3149-1613dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41182376 | |||||
| chrX:41182415
|
CT | C | 5 | a0001c0001t0001g0110a0001c0001t0001g0160a0001c0001t0004g0245others(2): Show | 5 | HG01496.hp2 HG02004.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3149-1570delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41182415 | |||||
| chrX:41182521
|
G | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3149-1477G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41182521 | ||||||
| chrX:41182830
|
C | T | 1 | a0001c0001t0005g0026 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3149-1168C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41182830 | ||||||
| chrX:41182937
|
G | GT | 7 | a0001c0001t0002g0072a0001c0001t0002g0099a0001c0001t0002g0100others(4): Show | 7 | HG02602.hp1 NA18955.hp1 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.3149-1046dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41182937 | |||||
| chrX:41182937
|
GT | G | 189 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.3149-1046delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41182937 | |||||
| chrX:41183015
|
T | C | 1 | a0001c0001t0003g0250 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3149-983T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41183015 | ||||||
| chrX:41183158
|
C | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3149-840C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41183158 | ||||||
| chrX:41183272
|
T | TA | 12 | a0001c0001t0001g0138a0001c0001t0001g0198a0001c0001t0001g0200others(9): Show | 12 | HG01496.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.3149-709dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41183272 | |||||
| chrX:41183272
|
TA | T | 5 | a0001c0001t0001g0110a0001c0001t0001g0144a0001c0001t0001g0187others(2): Show | 5 | HG00558.hp2 HG01975.hp1 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.3149-709delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41183272 | |||||
| chrX:41183272
|
TAAAAA | T | 1 | a0001c0001t0030g0275 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3149-713_3149-709d others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41183272 | |||||
| chrX:41183348
|
A | G | 1 | a0001c0001t0006g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3149-650A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41183348 | ||||||
| chrX:41183824
|
A | AT | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3149-164dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chrX | 41183824 | |||||
| chrX:41183840
|
T | C | 1 | a0001c0001t0003g0261 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3149-158T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41183840 | ||||||
| chrX:41183911
|
A | G | 1 | a0001c0001t0005g0054 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3149-87A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 21/44 | chrX | 41183911 | ||||||
| chrX:41184185
|
A | G | 2 | a0001c0001t0007g0044a0001c0001t0007g0045 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3279+57A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 22/44 | chrX | 41184185 | ||||||
| chrX:41184341
|
A | AT | 14 | a0001c0001t0002g0193a0001c0002t0002g0118a0001c0002t0002g0119others(11): Show | 14 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.3280-46dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 22/44 | INFO_REALIGN_3_PRIME | chrX | 41184341 | |||||
| chrX:41184691
|
T | C | 35 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(32): Show | 35 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.3558+16T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 23/44 | chrX | 41184691 | ||||||
| chrX:41184712
|
A | C | 1 | a0001c0001t0001g0217 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3558+37A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 23/44 | chrX | 41184712 | ||||||
| chrX:41185135
|
C | A | 5 | a0001c0001t0001g0134a0001c0001t0001g0146a0001c0001t0001g0149others(2): Show | 5 | NA18939.hp1 NA18946.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.3558+460C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 23/44 | chrX | 41185135 | ||||||
| chrX:41185175
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.3558+500A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 23/44 | chrX | 41185175 | ||||||
| chrX:41185248
|
T | A | 1 | a0001c0001t0001g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3558+573T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 23/44 | chrX | 41185248 | ||||||
| chrX:41185420
|
A | T | 1 | a0001c0001t0003g0261 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3558+745A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 23/44 | chrX | 41185420 | ||||||
| chrX:41185558
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3558+883A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 23/44 | chrX | 41185558 | ||||||
| chrX:41185650
|
A | AT | 6 | a0001c0001t0003g0271a0001c0001t0005g0012a0001c0001t0005g0063others(3): Show | 6 | HG02559.hp1 HG03195.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.3559-854dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 23/44 | INFO_REALIGN_3_PRIME | chrX | 41185650 | |||||
| chrX:41185650
|
AT | A | 1 | a0001c0001t0002g0053 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3559-854delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 23/44 | INFO_REALIGN_3_PRIME | chrX | 41185650 | |||||
| chrX:41185663
|
T | A | 1 | a0001c0001t0001g0115 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3559-854T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 23/44 | chrX | 41185663 | ||||||
| chrX:41185759
|
C | A | 7 | a0001c0001t0002g0046a0001c0001t0002g0087a0001c0001t0007g0017others(4): Show | 7 | HG00280.hp1 HG00733.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.3559-758C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 23/44 | chrX | 41185759 | ||||||
| chrX:41185902
|
G | GA | 1 | a0001c0001t0003g0271 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.3559-612dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 23/44 | INFO_REALIGN_3_PRIME | chrX | 41185902 | |||||
| chrX:41185925
|
T | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3559-592T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 23/44 | chrX | 41185925 | ||||||
| chrX:41186140
|
T | TG | 1 | a0001c0001t0002g0083 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3559-375dupG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 23/44 | INFO_REALIGN_3_PRIME | chrX | 41186140 | |||||
| chrX:41186183
|
A | G | 1 | a0001c0001t0003g0285 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3559-334A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 23/44 | chrX | 41186183 | ||||||
| chrX:41186185
|
A | C | 7 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0159others(4): Show | 7 | HG01081.hp1 HG01943.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.3559-332A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 23/44 | chrX | 41186185 | ||||||
| chrX:41186274
|
G | C | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3559-243G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 23/44 | chrX | 41186274 | ||||||
| chrX:41186480
|
A | C | 1 | a0001c0001t0004g0262 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3559-37A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 23/44 | chrX | 41186480 | ||||||
| chrX:41186750
|
CTATTAA | C | 12 | a0001c0002t0002g0118a0001c0002t0002g0119a0001c0002t0002g0120others(9): Show | 12 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3684+114_3684+119d others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 24/44 | INFO_REALIGN_3_PRIME | chrX | 41186750 | |||||
| chrX:41186830
|
A | AT | 31 | a0001c0001t0001g0114a0001c0001t0001g0124a0001c0001t0001g0125others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.3684+202dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 24/44 | INFO_REALIGN_3_PRIME | chrX | 41186830 | |||||
| chrX:41186830
|
A | ATT | 23 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(20): Show | 23 | HG00438.hp2 HG01891.hp2 HG02074.hp1 others(20): Show |
intron_variant | MODIFIER | c.3684+201_3684+202d others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 24/44 | INFO_REALIGN_3_PRIME | chrX | 41186830 | |||||
| chrX:41186958
|
C | G | 5 | a0001c0002t0002g0174a0001c0002t0002g0196a0001c0002t0002g0215others(2): Show | 5 | HG02970.hp2 HG03486.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.3684+316C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 24/44 | chrX | 41186958 | ||||||
| chrX:41186960
|
G | A | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3684+318G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 24/44 | chrX | 41186960 | ||||||
| chrX:41187118
|
C | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3684+476C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 24/44 | chrX | 41187118 | ||||||
| chrX:41187273
|
T | C | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3684+631T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 24/44 | chrX | 41187273 | ||||||
| chrX:41187280
|
C | G | 2 | a0001c0001t0003g0241a0001c0001t0030g0275 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3684+638C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 24/44 | chrX | 41187280 | ||||||
| chrX:41187441
|
A | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3685-551A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 24/44 | chrX | 41187441 | ||||||
| chrX:41187546
|
T | C | 1 | a0001c0001t0009g0233 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3685-446T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 24/44 | chrX | 41187546 | ||||||
| chrX:41187782
|
C | G | 9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 9 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.3685-210C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 24/44 | chrX | 41187782 | ||||||
| chrX:41187789
|
C | G | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3685-203C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 24/44 | chrX | 41187789 | ||||||
| chrX:41187829
|
C | CT | 14 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0153others(11): Show | 14 | HG02559.hp1 HG02615.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.3685-144dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 24/44 | INFO_REALIGN_3_PRIME | chrX | 41187829 | |||||
| chrX:41187829
|
CT | C | 2 | a0001c0001t0003g0280a0001c0001t0003g0289 | 2 | HG00323.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.3685-144delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 24/44 | INFO_REALIGN_3_PRIME | chrX | 41187829 | |||||
| chrX:41187829
|
CTT | C | 5 | a0001c0002t0002g0174a0001c0002t0002g0196a0001c0002t0002g0215others(2): Show | 5 | HG02970.hp2 HG03486.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.3685-145_3685-144d others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 24/44 | INFO_REALIGN_3_PRIME | chrX | 41187829 | |||||
| chrX:41187848
|
T | A | 1 | a0001c0001t0009g0025 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3685-144T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 24/44 | chrX | 41187848 | ||||||
| chrX:41188472
|
T | C | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3810+355T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 25/44 | chrX | 41188472 | ||||||
| chrX:41188700
|
T | G | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG00099.hp2 HG01123.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.3810+583T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 25/44 | chrX | 41188700 | ||||||
| chrX:41188736
|
T | C | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3811-573T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 25/44 | chrX | 41188736 | ||||||
| chrX:41189159
|
A | G | 4 | a0001c0003t0001g0130a0001c0003t0001g0150a0001c0003t0001g0151others(1): Show | 4 | NA18954.hp2 NA18957.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.3811-150A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 25/44 | chrX | 41189159 | ||||||
| chrX:41189183
|
A | G | 1 | a0001c0001t0005g0080 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3811-126A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 25/44 | chrX | 41189183 | ||||||
| chrX:41189813
|
GT | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3977+346delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41189813 | |||||
| chrX:41189831
|
CAG | C | 1 | a0001c0001t0002g0038 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3977+358_3977+359d others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41189831 | |||||
| chrX:41190478
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3977+1003T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41190478 | ||||||
| chrX:41190499
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3977+1024A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41190499 | ||||||
| chrX:41190508
|
G | A | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3977+1033G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41190508 | ||||||
| chrX:41190611
|
T | C | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.3977+1136T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41190611 | ||||||
| chrX:41190707
|
A | G | 2 | a0001c0001t0003g0269a0001c0001t0003g0271 | 2 | NA19066.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.3977+1232A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41190707 | ||||||
| chrX:41190708
|
G | A | 1 | a0001c0001t0027g0104 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3977+1233G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41190708 | ||||||
| chrX:41190820
|
T | A | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.3977+1345T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41190820 | ||||||
| chrX:41190827
|
T | C | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG00099.hp2 HG01123.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.3977+1352T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41190827 | ||||||
| chrX:41190925
|
T | A | 2 | a0001c0002t0002g0121a0001c0002t0002g0122 | 2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3977+1450T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41190925 | ||||||
| chrX:41191255
|
G | A | 4 | a0001c0001t0002g0024a0001c0001t0002g0041a0001c0001t0002g0042others(1): Show | 4 | HG00642.hp1 HG01081.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.3977+1780G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41191255 | ||||||
| chrX:41191281
|
A | T | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3977+1806A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41191281 | ||||||
| chrX:41191329
|
C | CA | 3 | a0001c0001t0002g0102a0001c0001t0005g0054a0001c0001t0005g0091 | 3 | HG02148.hp1 HG04184.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.3977+1874dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41191329 | |||||
| chrX:41191329
|
CA | C | 185 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(182): Show | 185 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.3977+1874delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41191329 | |||||
| chrX:41191329
|
CAA | C | 4 | a0001c0001t0001g0182a0001c0001t0004g0237a0001c0001t0008g0135others(1): Show | 4 | HG00140.hp1 HG01168.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.3977+1873_3977+187 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41191329 | |||||
| chrX:41191329
|
CAAA | C | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3977+1872_3977+187 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41191329 | |||||
| chrX:41191395
|
A | G | 1 | a0001c0001t0005g0067 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3977+1920A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41191395 | ||||||
| chrX:41191443
|
A | G | 1 | a0001c0001t0003g0274 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3977+1968A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41191443 | ||||||
| chrX:41191864
|
T | C | 197 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.3977+2389T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41191864 | ||||||
| chrX:41191893
|
T | C | 4 | a0001c0001t0002g0035a0001c0001t0002g0056a0001c0001t0002g0058others(1): Show | 4 | NA18944.hp1 NA18946.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.3977+2418T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41191893 | ||||||
| chrX:41192106
|
A | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3977+2631A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41192106 | ||||||
| chrX:41192107
|
C | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3977+2632C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41192107 | ||||||
| chrX:41192441
|
GT | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3977+2969delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41192441 | |||||
| chrX:41192527
|
T | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3977+3052T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41192527 | ||||||
| chrX:41192639
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3977+3164A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41192639 | ||||||
| chrX:41192933
|
TGAA | T | 2 | a0001c0001t0003g0238a0001c0001t0003g0244 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3978-3312_3978-331 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41192933 | |||||
| chrX:41193031
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3978-3220T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41193031 | ||||||
| chrX:41193042
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3978-3209C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41193042 | ||||||
| chrX:41193061
|
G | A | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.3978-3190G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41193061 | ||||||
| chrX:41193066
|
T | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(26): Show | 29 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.3978-3185T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41193066 | ||||||
| chrX:41193164
|
G | A | 31 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.3978-3087G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41193164 | ||||||
| chrX:41193199
|
G | GT | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.3978-3047dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41193199 | |||||
| chrX:41193501
|
G | GA | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.3978-2746dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41193501 | |||||
| chrX:41193520
|
C | CG | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.3978-2728dupG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41193520 | |||||
| chrX:41193544
|
T | TC | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.3978-2704dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41193544 | |||||
| chrX:41193588
|
G | A | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.3978-2663G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41193588 | ||||||
| chrX:41193663
|
C | CA | 1 | a0001c0001t0001g0188 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3978-2580dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41193663 | |||||
| chrX:41193663
|
CA | C | 1 | a0001c0001t0001g0146 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3978-2580delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41193663 | |||||
| chrX:41193670
|
A | T | 1 | a0001c0001t0001g0218 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3978-2581A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41193670 | ||||||
| chrX:41193671
|
A | T | 74 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0131others(71): Show | 74 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.3978-2580A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41193671 | ||||||
| chrX:41193754
|
A | G | 5 | a0001c0001t0002g0019a0001c0001t0002g0040a0001c0001t0009g0025others(2): Show | 5 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.3978-2497A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41193754 | ||||||
| chrX:41193939
|
A | AT | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.3978-2310dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41193939 | |||||
| chrX:41194020
|
T | C | 7 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(4): Show | 7 | HG01891.hp1 HG02895.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.3978-2231T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41194020 | ||||||
| chrX:41194109
|
C | T | 1 | a0001c0001t0002g0037 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3978-2142C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41194109 | ||||||
| chrX:41194111
|
C | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3978-2140C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41194111 | ||||||
| chrX:41194235
|
C | T | 1 | a0001c0001t0002g0069 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3978-2016C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41194235 | ||||||
| chrX:41194371
|
A | G | 1 | a0001c0001t0005g0054 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3978-1880A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41194371 | ||||||
| chrX:41194441
|
C | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3978-1810C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41194441 | ||||||
| chrX:41194547
|
T | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3978-1704T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41194547 | ||||||
| chrX:41194548
|
C | CT | 1 | a0001c0001t0018g0032 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.3978-1702dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41194548 | |||||
| chrX:41194602
|
C | T | 31 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.3978-1649C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41194602 | ||||||
| chrX:41194650
|
A | G | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.3978-1601A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41194650 | ||||||
| chrX:41194746
|
C | T | 1 | a0001c0001t0012g0082 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3978-1505C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41194746 | ||||||
| chrX:41194893
|
CA | C | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3978-1357delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41194893 | ||||||
| chrX:41194914
|
A | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3978-1337A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41194914 | ||||||
| chrX:41194935
|
A | T | 1 | a0001c0001t0031g0273 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3978-1316A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41194935 | ||||||
| chrX:41194980
|
A | G | 4 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(1): Show | 4 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.3978-1271A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41194980 | ||||||
| chrX:41194982
|
GT | G | 1 | a0001c0001t0001g0146 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3978-1265delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41194982 | |||||
| chrX:41195046
|
C | CTTTTTTT others(7): Show |
23 | a0001c0001t0003g0238a0001c0001t0003g0241a0001c0001t0003g0243others(20): Show | 23 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.3978-1197_3978-119 others(18): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41195046 | |||||
| chrX:41195046
|
C | CTTTTTTT others(8): Show |
30 | a0001c0001t0003g0239a0001c0001t0003g0254a0001c0001t0003g0281others(27): Show | 30 | HG00423.hp1 HG00597.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.3978-1197_3978-119 others(19): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41195046 | |||||
| chrX:41195046
|
C | CTTTTTTT others(9): Show |
3 | a0001c0001t0003g0276a0001c0001t0004g0242a0001c0001t0004g0257 | 3 | HG01074.hp1 HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.3978-1197_3978-119 others(20): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41195046 | |||||
| chrX:41195138
|
G | A | 1 | a0001c0001t0002g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3978-1113G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41195138 | ||||||
| chrX:41195203
|
A | AT | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.3978-1043dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41195203 | |||||
| chrX:41195248
|
G | GA | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3978-1002dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41195248 | |||||
| chrX:41195252
|
G | T | 1 | a0001c0001t0002g0049 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.3978-999G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41195252 | ||||||
| chrX:41195377
|
GT | G | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3978-871delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41195377 | |||||
| chrX:41195447
|
G | A | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.3978-804G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41195447 | ||||||
| chrX:41195493
|
T | TG | 2 | a0001c0001t0001g0170a0008c0006t0001g0002 | 2 | NA18959.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.3978-754dupG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41195493 | |||||
| chrX:41195510
|
G | GA | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3978-739dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41195510 | |||||
| chrX:41195523
|
G | A | 1 | a0001c0001t0004g0249 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3978-728G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41195523 | ||||||
| chrX:41195545
|
C | T | 1 | a0001c0001t0003g0264 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3978-706C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41195545 | ||||||
| chrX:41195668
|
A | G | 1 | a0001c0001t0003g0241 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3978-583A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41195668 | ||||||
| chrX:41195687
|
G | GA | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.3978-562dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41195687 | |||||
| chrX:41195687
|
GA | G | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3978-562delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41195687 | |||||
| chrX:41195714
|
G | GT | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.3978-534dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41195714 | |||||
| chrX:41195800
|
TG | T | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3978-447delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41195800 | |||||
| chrX:41195807
|
T | TG | 2 | a0001c0001t0001g0170a0008c0006t0001g0002 | 2 | NA18959.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.3978-440dupG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | INFO_REALIGN_3_PRIME | chrX | 41195807 | |||||
| chrX:41195838
|
C | CG | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3978-413_3978-412i others(3): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41195838 | ||||||
| chrX:41195879
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0145 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.3978-372G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41195879 | ||||||
| chrX:41196058
|
G | C | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.3978-193G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41196058 | ||||||
| chrX:41196164
|
C | A | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3978-87C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41196164 | ||||||
| chrX:41196165
|
A | C | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3978-86A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 26/44 | chrX | 41196165 | ||||||
| chrX:41196371
|
TA | T | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4086+16delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 27/44 | INFO_REALIGN_3_PRIME | chrX | 41196371 | |||||
| chrX:41196409
|
G | GA | 1 | a0001c0001t0001g0170 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4086+53dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 27/44 | INFO_REALIGN_3_PRIME | chrX | 41196409 | |||||
| chrX:41196414
|
AT | A | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4086+57delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 27/44 | INFO_REALIGN_3_PRIME | chrX | 41196414 | |||||
| chrX:41196429
|
G | GT | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4086+74dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 27/44 | INFO_REALIGN_3_PRIME | chrX | 41196429 | |||||
| chrX:41196446
|
A | G | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4086+87A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 27/44 | chrX | 41196446 | ||||||
| chrX:41196525
|
TG | T | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4087-64delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 27/44 | INFO_REALIGN_3_PRIME | chrX | 41196525 | |||||
| chrX:41196576
|
T | TC | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4087-15dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 27/44 | INFO_REALIGN_3_PRIME | chrX | 41196576 | |||||
| chrX:41196584
|
GT | G | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | splice_region_variant&intron_variant | LOW | c.4087-5delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 27/44 | INFO_REALIGN_3_PRIME | chrX | 41196584 | |||||
| chrX:41196751
|
TA | T | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4233+15delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 28/44 | INFO_REALIGN_3_PRIME | chrX | 41196751 | |||||
| chrX:41196801
|
A | G | 7 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(4): Show | 7 | HG01891.hp1 HG02895.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.4233+63A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 28/44 | chrX | 41196801 | ||||||
| chrX:41196986
|
A | AT | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4233+252dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 28/44 | INFO_REALIGN_3_PRIME | chrX | 41196986 | |||||
| chrX:41197150
|
A | G | 197 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.4234-214A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 28/44 | chrX | 41197150 | ||||||
| chrX:41197181
|
A | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.4234-183A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 28/44 | chrX | 41197181 | ||||||
| chrX:41197331
|
T | TC | 10 | a0001c0001t0001g0170a0001c0001t0001g0218a0001c0001t0002g0057others(7): Show | 10 | HG01175.hp1 HG01978.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.4234-24dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 28/44 | INFO_REALIGN_3_PRIME | chrX | 41197331 | |||||
| chrX:41197339
|
C | T | 1 | a0001c0001t0003g0283 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.4234-25C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 28/44 | chrX | 41197339 | ||||||
| chrX:41197346
|
A | AC | 2 | a0001c0001t0002g0085a0001c0001t0002g0101 | 2 | NA18979.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.4234-12dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 28/44 | INFO_REALIGN_3_PRIME | chrX | 41197346 | |||||
| chrX:41197592
|
TATC | T | 5 | a0001c0001t0008g0103a0001c0001t0008g0135a0001c0001t0008g0136others(2): Show | 5 | HG01070.hp2 HG01168.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.4380+85_4380+87del others(3): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 29/44 | INFO_REALIGN_3_PRIME | chrX | 41197592 | |||||
| chrX:41197624
|
CTTT | C | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.4380+118_4380+120d others(5): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 29/44 | INFO_REALIGN_3_PRIME | chrX | 41197624 | |||||
| chrX:41197773
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4380+263G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 29/44 | chrX | 41197773 | ||||||
| chrX:41197852
|
G | GA | 57 | a0001c0001t0002g0210a0001c0001t0003g0238a0001c0001t0003g0239others(54): Show | 57 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.4380+354dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 29/44 | INFO_REALIGN_3_PRIME | chrX | 41197852 | |||||
| chrX:41197852
|
GA | G | 2 | a0001c0001t0002g0036a0001c0001t0002g0101 | 2 | HG00408.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.4380+354delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 29/44 | INFO_REALIGN_3_PRIME | chrX | 41197852 | |||||
| chrX:41197968
|
C | T | 1 | a0001c0001t0002g0013 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4380+458C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 29/44 | chrX | 41197968 | ||||||
| chrX:41198009
|
T | C | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4380+499T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 29/44 | chrX | 41198009 | ||||||
| chrX:41198073
|
CT | C | 1 | a0001c0001t0002g0101 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.4381-452delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 29/44 | INFO_REALIGN_3_PRIME | chrX | 41198073 | |||||
| chrX:41198118
|
CTG | C | 31 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.4381-408_4381-407d others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 29/44 | INFO_REALIGN_3_PRIME | chrX | 41198118 | |||||
| chrX:41198155
|
G | GT | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4381-367dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 29/44 | INFO_REALIGN_3_PRIME | chrX | 41198155 | |||||
| chrX:41198366
|
TTTTGAAG others(58): Show |
T | 74 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0131others(71): Show | 74 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.4381-161_4381-97de others(66): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 29/44 | chrX | 41198366 | ||||||
| chrX:41198468
|
C | CT | 1 | a0001c0001t0012g0082 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4381-51dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 29/44 | INFO_REALIGN_3_PRIME | chrX | 41198468 | |||||
| chrX:41198769
|
A | G | 2 | a0001c0001t0010g0156a0001c0001t0010g0157 | 2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.4603+19A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 30/44 | chrX | 41198769 | ||||||
| chrX:41198770
|
T | G | 1 | a0001c0001t0001g0158 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.4603+20T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 30/44 | chrX | 41198770 | ||||||
| chrX:41198790
|
A | G | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4603+40A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 30/44 | chrX | 41198790 | ||||||
| chrX:41198879
|
G | A | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.4603+129G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 30/44 | chrX | 41198879 | ||||||
| chrX:41198886
|
A | T | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.4603+136A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 30/44 | chrX | 41198886 | ||||||
| chrX:41198992
|
GC | G | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4603+244delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chrX | 41198992 | |||||
| chrX:41199014
|
T | TC | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4603+265dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chrX | 41199014 | |||||
| chrX:41199155
|
T | G | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.4603+405T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 30/44 | chrX | 41199155 | ||||||
| chrX:41199189
|
AAAAAG | A | 3 | a0001c0002t0002g0122a0002c0005t0011g0235a0002c0005t0011g0236 | 3 | HG01891.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4603+459_4603+463d others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chrX | 41199189 | |||||
| chrX:41199299
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4603+549G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 30/44 | chrX | 41199299 | ||||||
| chrX:41199603
|
A | AT | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4603+858dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chrX | 41199603 | |||||
| chrX:41199658
|
G | GC | 1 | a0003c0010t0002g0074 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4603+910dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chrX | 41199658 | |||||
| chrX:41199790
|
C | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.4603+1040C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 30/44 | chrX | 41199790 | ||||||
| chrX:41200026
|
G | A | 1 | a0001c0001t0015g0021 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4604-1034G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 30/44 | chrX | 41200026 | ||||||
| chrX:41200216
|
AT | A | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(114): Show | 117 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.4604-834delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chrX | 41200216 | |||||
| chrX:41200311
|
T | C | 1 | a0001c0001t0016g0185 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4604-749T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 30/44 | chrX | 41200311 | ||||||
| chrX:41201009
|
G | GA | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4604-48dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chrX | 41201009 | |||||
| chrX:41201305
|
T | C | 2 | a0001c0001t0001g0192a0001c0001t0025g0133 | 2 | HG03654.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.4824+25T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41201305 | ||||||
| chrX:41201360
|
A | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.4824+80A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41201360 | ||||||
| chrX:41201455
|
T | C | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4824+175T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41201455 | ||||||
| chrX:41201552
|
G | GA | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+277dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41201552 | |||||
| chrX:41201681
|
C | CA | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+403dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41201681 | |||||
| chrX:41201684
|
C | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG01167.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.4824+404C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41201684 | ||||||
| chrX:41201745
|
TG | T | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+467delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41201745 | |||||
| chrX:41201871
|
T | G | 1 | a0001c0001t0001g0221 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.4824+591T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41201871 | ||||||
| chrX:41201966
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4824+686G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41201966 | ||||||
| chrX:41201970
|
C | CA | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+701dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41201970 | |||||
| chrX:41201970
|
CA | C | 1 | a0001c0001t0001g0170 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4824+701delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41201970 | |||||
| chrX:41202023
|
A | AGT | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+744_4824+745d others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41202023 | |||||
| chrX:41202031
|
TTG | T | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+752_4824+753d others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41202031 | ||||||
| chrX:41202037
|
T | G | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+757T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41202037 | ||||||
| chrX:41202064
|
TTGA | T | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+786_4824+788d others(5): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41202064 | |||||
| chrX:41202080
|
AT | A | 1 | a0001c0001t0001g0170 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4824+805delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41202080 | |||||
| chrX:41202152
|
T | C | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.4824+872T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41202152 | ||||||
| chrX:41202153
|
G | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.4824+873G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41202153 | ||||||
| chrX:41202155
|
G | C | 291 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.4824+875G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41202155 | ||||||
| chrX:41202248
|
G | A | 1 | a0001c0001t0001g0125 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4824+968G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41202248 | ||||||
| chrX:41202253
|
C | CCAA | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+973_4824+974i others(5): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41202253 | ||||||
| chrX:41202255
|
T | TAGG | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+975_4824+976i others(5): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41202255 | ||||||
| chrX:41202256
|
G | C | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+976G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41202256 | ||||||
| chrX:41202260
|
CA | C | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+984delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41202260 | |||||
| chrX:41202438
|
CT | C | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+1162delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41202438 | |||||
| chrX:41202446
|
GT | G | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+1169delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41202446 | |||||
| chrX:41202610
|
TA | T | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+1331delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41202610 | ||||||
| chrX:41202611
|
A | G | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(134): Show | 137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.4824+1331A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41202611 | ||||||
| chrX:41202627
|
AT | A | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+1348delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41202627 | ||||||
| chrX:41202656
|
T | TC | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+1377dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41202656 | |||||
| chrX:41202664
|
TA | T | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+1392delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41202664 | |||||
| chrX:41202698
|
T | TATTA | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+1419_4824+142 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41202698 | |||||
| chrX:41202734
|
TA | T | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+1456delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41202734 | |||||
| chrX:41202762
|
CAT | C | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+1486_4824+148 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41202762 | |||||
| chrX:41202774
|
AT | A | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+1495delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41202774 | ||||||
| chrX:41202783
|
T | TA | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+1506dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41202783 | |||||
| chrX:41202792
|
G | T | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+1512G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41202792 | ||||||
| chrX:41202793
|
T | TA | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+1514dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41202793 | |||||
| chrX:41202795
|
G | A | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+1515G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41202795 | ||||||
| chrX:41202815
|
C | CAAG | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+1539_4824+154 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41202815 | |||||
| chrX:41202820
|
A | G | 2 | a0001c0001t0002g0078a0001c0001t0002g0088 | 2 | NA18951.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.4824+1540A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41202820 | ||||||
| chrX:41202849
|
A | G | 2 | a0001c0001t0001g0138a0001c0001t0001g0200 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4824+1569A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41202849 | ||||||
| chrX:41202945
|
TTG | T | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+1666_4824+166 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41202945 | ||||||
| chrX:41202950
|
T | G | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+1670T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41202950 | ||||||
| chrX:41203021
|
GTTGTC | G | 1 | a0008c0006t0001g0002 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4824+1743_4824+174 others(9): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41203021 | |||||
| chrX:41203169
|
CTGT | C | 13 | a0001c0002t0002g0118a0001c0002t0002g0119a0001c0002t0002g0120others(10): Show | 13 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.4824+1894_4824+189 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41203169 | |||||
| chrX:41203601
|
A | T | 1 | a0001c0001t0002g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.4825-1702A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41203601 | ||||||
| chrX:41203782
|
C | T | 1 | a0001c0001t0005g0066 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4825-1521C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41203782 | ||||||
| chrX:41203859
|
C | T | 1 | a0001c0001t0003g0289 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4825-1444C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41203859 | ||||||
| chrX:41203904
|
G | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | NA19012.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.4825-1399G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41203904 | ||||||
| chrX:41203926
|
G | A | 1 | a0001c0001t0002g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4825-1377G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41203926 | ||||||
| chrX:41203991
|
T | C | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.4825-1312T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41203991 | ||||||
| chrX:41204352
|
C | T | 1 | a0001c0001t0019g0018 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4825-951C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41204352 | ||||||
| chrX:41204413
|
G | GT | 1 | a0001c0001t0015g0021 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4825-874dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41204413 | |||||
| chrX:41204413
|
GT | G | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.4825-874delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41204413 | |||||
| chrX:41204413
|
GTT | G | 3 | a0001c0001t0013g0180a0001c0001t0028g0179a0004c0009t0006g0116 | 3 | HG02559.hp1 HG03195.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.4825-875_4825-874d others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41204413 | |||||
| chrX:41204429
|
T | TA | 1 | a0001c0001t0003g0293 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.4825-872dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41204429 | |||||
| chrX:41204492
|
A | T | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4825-811A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41204492 | ||||||
| chrX:41204542
|
C | A | 3 | a0001c0001t0004g0246a0001c0001t0004g0247a0001c0001t0004g0256 | 3 | NA18941.hp2 NA18975.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.4825-761C>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41204542 | ||||||
| chrX:41204543
|
A | T | 3 | a0001c0001t0004g0246a0001c0001t0004g0247a0001c0001t0004g0256 | 3 | NA18941.hp2 NA18975.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.4825-760A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41204543 | ||||||
| chrX:41204574
|
T | TAC | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.4825-728_4825-727i others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41204574 | |||||
| chrX:41204730
|
G | A | 193 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.4825-573G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41204730 | ||||||
| chrX:41204897
|
C | T | 1 | a0001c0001t0027g0104 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4825-406C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41204897 | ||||||
| chrX:41204902
|
C | G | 1 | a0001c0001t0003g0293 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.4825-401C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41204902 | ||||||
| chrX:41204931
|
A | G | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(114): Show | 117 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.4825-372A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41204931 | ||||||
| chrX:41204947
|
C | T | 1 | a0001c0001t0009g0061 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4825-356C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41204947 | ||||||
| chrX:41204956
|
A | G | 31 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.4825-347A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | chrX | 41204956 | ||||||
| chrX:41205055
|
TA | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.4825-245delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41205055 | |||||
| chrX:41205155
|
CACTA | C | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.4825-146_4825-143d others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 41205155 | |||||
| chrX:41205527
|
CT | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5015+36delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41205527 | |||||
| chrX:41205587
|
CT | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5015+101delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41205587 | |||||
| chrX:41205628
|
GGT | G | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5015+137_5015+138d others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41205628 | |||||
| chrX:41205631
|
G | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5015+138G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41205631 | ||||||
| chrX:41205633
|
G | GT | 7 | a0001c0001t0001g0154a0001c0001t0001g0214a0001c0001t0001g0219others(4): Show | 7 | HG00408.hp1 HG01099.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5015+157dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41205633 | |||||
| chrX:41205633
|
G | GTT | 1 | a0001c0001t0001g0158 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.5015+156_5015+157d others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41205633 | |||||
| chrX:41205633
|
GT | G | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.5015+157delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41205633 | |||||
| chrX:41205685
|
TA | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5015+194delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41205685 | |||||
| chrX:41205856
|
AT | A | 1 | a0001c0001t0012g0082 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5015+373delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41205856 | |||||
| chrX:41205861
|
TTTTTTCT others(13): Show |
T | 6 | a0001c0001t0001g0209a0001c0001t0008g0103a0001c0001t0008g0135others(3): Show | 6 | HG01070.hp2 HG01168.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.5015+388_5015+407d others(22): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41205861 | |||||
| chrX:41205874
|
T | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5015+381T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41205874 | ||||||
| chrX:41205875
|
C | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5015+382C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41205875 | ||||||
| chrX:41205880
|
T | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5015+387T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41205880 | ||||||
| chrX:41205887
|
C | CT | 35 | a0001c0001t0003g0238a0001c0001t0003g0243a0001c0001t0003g0244others(32): Show | 35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.5015+401dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41205887 | |||||
| chrX:41205887
|
C | CTT | 19 | a0001c0001t0003g0241a0001c0001t0003g0263a0001c0001t0004g0242others(16): Show | 19 | HG00423.hp1 HG00597.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.5015+400_5015+401d others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41205887 | |||||
| chrX:41205887
|
C | CTTT | 1 | a0001c0001t0003g0239 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5015+399_5015+401d others(5): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41205887 | |||||
| chrX:41205887
|
C | CTTTTT | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5015+397_5015+401d others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41205887 | |||||
| chrX:41205895
|
C | CT | 2 | a0001c0001t0007g0017a0001c0001t0017g0023 | 2 | HG00280.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.5015+414dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41205895 | |||||
| chrX:41205895
|
C | T | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.5015+402C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41205895 | ||||||
| chrX:41205895
|
CT | C | 2 | a0001c0001t0006g0128a0004c0009t0006g0116 | 2 | HG01515.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.5015+414delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41205895 | |||||
| chrX:41205980
|
TC | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5015+490delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41205980 | |||||
| chrX:41206022
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.5015+529C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41206022 | ||||||
| chrX:41206047
|
C | T | 4 | a0001c0003t0001g0130a0001c0003t0001g0150a0001c0003t0001g0151others(1): Show | 4 | NA18954.hp2 NA18957.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.5015+554C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41206047 | ||||||
| chrX:41206048
|
G | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.5015+555G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41206048 | ||||||
| chrX:41206066
|
AT | A | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5015+578delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41206066 | |||||
| chrX:41206199
|
T | A | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5015+706T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41206199 | ||||||
| chrX:41206223
|
A | C | 8 | a0001c0002t0002g0118a0001c0002t0002g0119a0001c0002t0002g0120others(5): Show | 8 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.5015+730A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41206223 | ||||||
| chrX:41206227
|
CT | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5015+736delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41206227 | |||||
| chrX:41206307
|
T | C | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0026g0166 | 3 | HG00408.hp2 HG02129.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.5015+814T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41206307 | ||||||
| chrX:41206352
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG02922.hp2 HG02976.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.5015+859C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41206352 | ||||||
| chrX:41206359
|
T | C | 1 | a0001c0001t0003g0264 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.5015+866T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41206359 | ||||||
| chrX:41206382
|
AT | A | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5015+895delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41206382 | |||||
| chrX:41206467
|
CT | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5015+977delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41206467 | |||||
| chrX:41206499
|
A | G | 1 | a0001c0001t0009g0025 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.5015+1006A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41206499 | ||||||
| chrX:41206578
|
T | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.5015+1085T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41206578 | ||||||
| chrX:41206627
|
C | G | 74 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0131others(71): Show | 74 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.5015+1134C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41206627 | ||||||
| chrX:41206654
|
TG | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5015+1163delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41206654 | |||||
| chrX:41206752
|
T | A | 33 | a0001c0001t0003g0250a0001c0001t0003g0253a0001c0001t0003g0259others(30): Show | 33 | HG00423.hp1 HG00597.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.5015+1259T>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41206752 | ||||||
| chrX:41206778
|
AT | A | 2 | a0001c0001t0003g0239a0001c0001t0013g0180 | 2 | HG02559.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.5015+1296delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41206778 | |||||
| chrX:41207003
|
C | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.5015+1510C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41207003 | ||||||
| chrX:41207006
|
G | C | 1 | a0001c0001t0009g0233 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.5015+1513G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41207006 | ||||||
| chrX:41207045
|
GCT | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.5015+1553_5015+155 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41207045 | ||||||
| chrX:41207079
|
C | CT | 9 | a0001c0001t0002g0057a0001c0001t0002g0096a0001c0001t0002g0106others(6): Show | 9 | HG01175.hp1 HG01496.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.5015+1612dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41207079 | |||||
| chrX:41207079
|
C | CTT | 8 | a0001c0001t0002g0193a0001c0001t0022g0014a0001c0002t0002g0174others(5): Show | 8 | HG02615.hp1 HG02723.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.5015+1611_5015+161 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41207079 | |||||
| chrX:41207079
|
C | CTTT | 8 | a0001c0002t0002g0118a0001c0002t0002g0119a0001c0002t0002g0121others(5): Show | 8 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.5015+1610_5015+161 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41207079 | |||||
| chrX:41207079
|
C | CTTTT | 1 | a0001c0002t0002g0120 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5015+1609_5015+161 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41207079 | |||||
| chrX:41207079
|
CT | C | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.5015+1612delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41207079 | |||||
| chrX:41207079
|
CTT | C | 106 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(103): Show | 106 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.5015+1611_5015+161 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41207079 | |||||
| chrX:41207079
|
CTTT | C | 5 | a0001c0001t0001g0170a0001c0001t0001g0192a0001c0001t0001g0198others(2): Show | 5 | HG03654.hp1 HG04199.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.5015+1610_5015+161 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41207079 | |||||
| chrX:41207111
|
T | TA | 1 | a0001c0001t0005g0051 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.5015+1619dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41207111 | |||||
| chrX:41207134
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5015+1641G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41207134 | ||||||
| chrX:41207246
|
G | A | 3 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0012g0107 | 3 | HG01496.hp1 HG02486.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5015+1753G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41207246 | ||||||
| chrX:41207286
|
T | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0200 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.5015+1793T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41207286 | ||||||
| chrX:41207331
|
C | T | 4 | a0001c0001t0002g0036a0001c0001t0002g0039a0001c0001t0002g0053others(1): Show | 4 | HG00408.hp1 NA18966.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.5015+1838C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41207331 | ||||||
| chrX:41207360
|
C | CA | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5015+1868dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41207360 | |||||
| chrX:41207380
|
TG | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5015+1889delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41207380 | |||||
| chrX:41207389
|
A | G | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5015+1896A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41207389 | ||||||
| chrX:41207707
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5015+2214C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41207707 | ||||||
| chrX:41207719
|
A | G | 3 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096 | 3 | HG02572.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5015+2226A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41207719 | ||||||
| chrX:41207791
|
CT | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5015+2302delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41207791 | |||||
| chrX:41207935
|
CT | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5015+2445delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41207935 | |||||
| chrX:41208037
|
G | GT | 10 | a0001c0001t0002g0024a0001c0001t0002g0060a0001c0001t0002g0065others(7): Show | 10 | HG00642.hp1 HG01081.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.5016-2458dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41208037 | |||||
| chrX:41208037
|
GT | G | 2 | a0001c0001t0001g0170a0001c0001t0017g0023 | 2 | NA18959.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.5016-2458delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41208037 | |||||
| chrX:41208037
|
GTT | G | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5016-2459_5016-245 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41208037 | |||||
| chrX:41208110
|
G | A | 73 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0131others(70): Show | 73 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.5016-2399G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41208110 | ||||||
| chrX:41208304
|
C | T | 1 | a0001c0001t0013g0180 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5016-2205C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41208304 | ||||||
| chrX:41208589
|
CT | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5016-1917delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41208589 | |||||
| chrX:41208620
|
A | G | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5016-1889A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41208620 | ||||||
| chrX:41208632
|
GC | G | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5016-1875delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41208632 | |||||
| chrX:41208677
|
A | AT | 1 | a0001c0001t0001g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5016-1822dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41208677 | |||||
| chrX:41208719
|
T | G | 1 | a0001c0001t0003g0291 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.5016-1790T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41208719 | ||||||
| chrX:41208769
|
G | A | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.5016-1740G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41208769 | ||||||
| chrX:41208776
|
C | T | 192 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(189): Show | 192 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.5016-1733C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41208776 | ||||||
| chrX:41208781
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5016-1728C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41208781 | ||||||
| chrX:41208808
|
C | CA | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5016-1700dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41208808 | |||||
| chrX:41208862
|
CA | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5016-1645delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41208862 | |||||
| chrX:41208930
|
G | A | 2 | a0001c0001t0010g0156a0001c0001t0010g0157 | 2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.5016-1579G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41208930 | ||||||
| chrX:41208971
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.5016-1538A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41208971 | ||||||
| chrX:41209003
|
C | T | 3 | a0001c0001t0005g0012a0001c0001t0005g0063a0001c0001t0005g0064 | 3 | NA18939.hp2 NA18960.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.5016-1506C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41209003 | ||||||
| chrX:41209050
|
AC | A | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5016-1455delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41209050 | |||||
| chrX:41209105
|
A | G | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5016-1404A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41209105 | ||||||
| chrX:41209196
|
CA | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5016-1309delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41209196 | |||||
| chrX:41209226
|
T | C | 1 | a0001c0001t0003g0287 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.5016-1283T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41209226 | ||||||
| chrX:41209332
|
AT | A | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5016-1172delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41209332 | |||||
| chrX:41209360
|
TG | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5016-1148delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41209360 | ||||||
| chrX:41209502
|
CT | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5016-1005delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41209502 | |||||
| chrX:41209571
|
CT | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5016-934delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41209571 | |||||
| chrX:41209651
|
TG | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5016-856delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41209651 | |||||
| chrX:41209679
|
T | G | 5 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0048others(2): Show | 5 | HG02451.hp2 HG02723.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.5016-830T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41209679 | ||||||
| chrX:41209717
|
T | C | 4 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(1): Show | 4 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.5016-792T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41209717 | ||||||
| chrX:41209856
|
AT | A | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5016-651delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41209856 | |||||
| chrX:41209931
|
A | G | 1 | a0001c0001t0003g0276 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5016-578A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41209931 | ||||||
| chrX:41210350
|
CT | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5016-152delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41210350 | |||||
| chrX:41210416
|
G | A | 3 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0012g0107 | 3 | HG01496.hp1 HG02486.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5016-93G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | chrX | 41210416 | ||||||
| chrX:41210425
|
C | CT | 1 | a0001c0001t0003g0271 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.5016-76dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 32/44 | INFO_REALIGN_3_PRIME | chrX | 41210425 | |||||
| chrX:41210744
|
AT | A | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5189+67delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41210744 | |||||
| chrX:41210759
|
T | TA | 33 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.5189+78dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41210759 | |||||
| chrX:41210840
|
TG | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5189+162delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41210840 | |||||
| chrX:41210842
|
G | T | 1 | a0001c0001t0003g0276 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5189+160G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41210842 | ||||||
| chrX:41210975
|
CT | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5189+296delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41210975 | |||||
| chrX:41210999
|
CT | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5189+323delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41210999 | |||||
| chrX:41211056
|
G | A | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.5189+374G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41211056 | ||||||
| chrX:41211124
|
T | TG | 1 | a0006c0007t0020g0098 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.5189+445dupG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41211124 | |||||
| chrX:41211136
|
C | CA | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5189+455dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41211136 | |||||
| chrX:41211251
|
A | G | 4 | a0001c0001t0002g0037a0001c0001t0002g0038a0001c0001t0002g0059others(1): Show | 4 | NA18940.hp1 NA18945.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.5189+569A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41211251 | ||||||
| chrX:41211332
|
A | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.5189+650A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41211332 | ||||||
| chrX:41211534
|
A | G | 3 | a0001c0001t0001g0197a0001c0001t0001g0218a0001c0001t0001g0219 | 3 | HG02055.hp1 HG02280.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.5189+852A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41211534 | ||||||
| chrX:41211549
|
TA | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5189+874delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41211549 | |||||
| chrX:41211563
|
AC | A | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5189+886delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41211563 | |||||
| chrX:41211600
|
T | C | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.5189+918T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41211600 | ||||||
| chrX:41211630
|
GC | G | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5189+951delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41211630 | |||||
| chrX:41211653
|
G | A | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.5189+971G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41211653 | ||||||
| chrX:41211682
|
C | CG | 1 | a0006c0007t0020g0098 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.5189+1002dupG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41211682 | |||||
| chrX:41211691
|
G | A | 1 | a0001c0001t0003g0290 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5189+1009G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41211691 | ||||||
| chrX:41211700
|
G | A | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5189+1018G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41211700 | ||||||
| chrX:41211721
|
GC | G | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5189+1045delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41211721 | |||||
| chrX:41211835
|
G | A | 2 | a0001c0001t0010g0156a0001c0001t0010g0157 | 2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.5189+1153G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41211835 | ||||||
| chrX:41211837
|
TG | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5189+1162delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41211837 | |||||
| chrX:41211848
|
G | GC | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5189+1172dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41211848 | |||||
| chrX:41211933
|
GC | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.5189+1254delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41211933 | |||||
| chrX:41212095
|
C | CT | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5189+1417dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41212095 | |||||
| chrX:41212137
|
G | C | 6 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG00099.hp2 HG01123.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.5189+1455G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41212137 | ||||||
| chrX:41212214
|
G | C | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5189+1532G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41212214 | ||||||
| chrX:41212226
|
T | C | 1 | a0001c0001t0001g0171 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.5189+1544T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41212226 | ||||||
| chrX:41212289
|
TC | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5189+1610delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41212289 | |||||
| chrX:41212313
|
C | T | 5 | a0001c0002t0002g0174a0001c0002t0002g0196a0001c0002t0002g0215others(2): Show | 5 | HG02970.hp2 HG03486.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.5189+1631C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41212313 | ||||||
| chrX:41212330
|
G | GC | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5189+1650dupC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41212330 | |||||
| chrX:41212392
|
TC | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5189+1713delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41212392 | |||||
| chrX:41212409
|
T | C | 1 | a0001c0001t0003g0281 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.5189+1727T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41212409 | ||||||
| chrX:41212459
|
T | TA | 151 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.5189+1793dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41212459 | |||||
| chrX:41212459
|
T | TAA | 57 | a0001c0001t0002g0210a0001c0001t0003g0239a0001c0001t0003g0241others(54): Show | 57 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.5189+1792_5189+179 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41212459 | |||||
| chrX:41212459
|
T | TAAA | 1 | a0001c0001t0003g0238 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5189+1791_5189+179 others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41212459 | |||||
| chrX:41212459
|
T | TTA | 1 | a0001c0001t0003g0292 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5189+1777_5189+177 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41212459 | ||||||
| chrX:41212459
|
TA | T | 1 | a0001c0001t0014g0279 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.5189+1793delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41212459 | |||||
| chrX:41212476
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0213 | 2 | HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.5189+1794G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41212476 | ||||||
| chrX:41212479
|
TA | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5189+1804delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41212479 | |||||
| chrX:41212491
|
AAT | A | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5189+1811_5189+181 others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41212491 | |||||
| chrX:41212494
|
A | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5189+1812A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41212494 | ||||||
| chrX:41212531
|
ATTGT | A | 1 | a0001c0004t0002g0211 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5189+1853_5189+185 others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41212531 | |||||
| chrX:41212637
|
GT | G | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5190-1929delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41212637 | |||||
| chrX:41212759
|
TG | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5190-1804delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41212759 | |||||
| chrX:41212798
|
T | C | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.5190-1770T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41212798 | ||||||
| chrX:41212878
|
T | C | 1 | a0001c0008t0002g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5190-1690T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41212878 | ||||||
| chrX:41212941
|
A | G | 1 | a0001c0001t0003g0259 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5190-1627A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41212941 | ||||||
| chrX:41212972
|
T | TA | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5190-1591dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41212972 | |||||
| chrX:41213041
|
AT | A | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5190-1524delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41213041 | |||||
| chrX:41213062
|
T | C | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5190-1506T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41213062 | ||||||
| chrX:41213222
|
AG | A | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5190-1344delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41213222 | |||||
| chrX:41213414
|
A | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5190-1154A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41213414 | ||||||
| chrX:41213487
|
G | A | 1 | a0001c0001t0003g0293 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.5190-1081G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41213487 | ||||||
| chrX:41213621
|
T | G | 74 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0131others(71): Show | 74 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.5190-947T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41213621 | ||||||
| chrX:41213629
|
TG | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5190-937delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41213629 | |||||
| chrX:41213677
|
CT | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5190-886delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41213677 | |||||
| chrX:41213705
|
CT | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5190-859delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41213705 | |||||
| chrX:41213770
|
A | G | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.5190-798A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41213770 | ||||||
| chrX:41213831
|
CT | C | 4 | a0001c0002t0002g0174a0001c0002t0002g0196a0001c0002t0021g0195others(1): Show | 4 | HG02970.hp2 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.5190-731delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41213831 | |||||
| chrX:41213852
|
TC | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5190-714delC | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41213852 | |||||
| chrX:41213895
|
A | G | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.5190-673A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41213895 | ||||||
| chrX:41214355
|
T | TA | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5190-212dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41214355 | |||||
| chrX:41214360
|
G | A | 1 | a0001c0002t0002g0121 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5190-208G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41214360 | ||||||
| chrX:41214364
|
C | T | 4 | a0001c0001t0002g0036a0001c0001t0002g0039a0001c0001t0002g0053others(1): Show | 4 | HG00408.hp1 NA18966.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.5190-204C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41214364 | ||||||
| chrX:41214401
|
C | T | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5190-167C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41214401 | ||||||
| chrX:41214406
|
A | T | 1 | a0001c0001t0003g0281 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.5190-162A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41214406 | ||||||
| chrX:41214425
|
G | A | 2 | a0001c0001t0013g0180a0001c0001t0028g0179 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.5190-143G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41214425 | ||||||
| chrX:41214476
|
TA | T | 1 | a0001c0001t0001g0010 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.5190-82delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 41214476 | |||||
| chrX:41214477
|
A | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.5190-91A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41214477 | ||||||
| chrX:41214481
|
A | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.5190-87A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 33/44 | chrX | 41214481 | ||||||
| chrX:41214744
|
CA | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5331+36delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 34/44 | chrX | 41214744 | ||||||
| chrX:41214769
|
GT | G | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5331+67delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 34/44 | INFO_REALIGN_3_PRIME | chrX | 41214769 | |||||
| chrX:41214771
|
T | C | 1 | a0001c0002t0002g0121 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5331+62T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 34/44 | chrX | 41214771 | ||||||
| chrX:41215188
|
T | C | 1 | a0001c0001t0003g0264 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.5331+479T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 34/44 | chrX | 41215188 | ||||||
| chrX:41215597
|
T | G | 2 | a0001c0001t0013g0180a0001c0001t0028g0179 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.5332-302T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 34/44 | chrX | 41215597 | ||||||
| chrX:41215633
|
C | T | 1 | a0001c0001t0003g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5332-266C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 34/44 | chrX | 41215633 | ||||||
| chrX:41215808
|
CTT | C | 1 | a0001c0001t0005g0080 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5332-90_5332-89del others(2): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 34/44 | chrX | 41215808 | ||||||
| chrX:41215836
|
G | GT | 59 | a0001c0001t0001g0007a0001c0001t0001g0114a0001c0001t0001g0146others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.5332-50dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 34/44 | INFO_REALIGN_3_PRIME | chrX | 41215836 | |||||
| chrX:41215836
|
G | GTT | 3 | a0001c0001t0003g0253a0001c0001t0003g0267a0001c0001t0004g0268 | 3 | HG04184.hp1 NA19011.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.5332-51_5332-50dup others(2): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 34/44 | INFO_REALIGN_3_PRIME | chrX | 41215836 | |||||
| chrX:41215836
|
GT | G | 1 | a0001c0001t0006g0148 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.5332-50delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 34/44 | INFO_REALIGN_3_PRIME | chrX | 41215836 | |||||
| chrX:41216707
|
G | A | 25 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0158others(22): Show | 25 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.6085+55G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 35/44 | chrX | 41216707 | ||||||
| chrX:41216916
|
ACCTGTAG others(12): Show |
A | 1 | a0001c0001t0010g0157 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.6086-283_6086-265d others(21): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 35/44 | INFO_REALIGN_3_PRIME | chrX | 41216916 | |||||
| chrX:41216955
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6086-265C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 35/44 | chrX | 41216955 | ||||||
| chrX:41217032
|
C | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.6086-188C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 35/44 | chrX | 41217032 | ||||||
| chrX:41217049
|
A | G | 1 | a0001c0001t0028g0179 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.6086-171A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 35/44 | chrX | 41217049 | ||||||
| chrX:41217088
|
G | T | 1 | a0001c0001t0003g0250 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.6086-132G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 35/44 | chrX | 41217088 | ||||||
| chrX:41217372
|
T | G | 1 | a0001c0001t0001g0230 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.6209+29T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 36/44 | chrX | 41217372 | ||||||
| chrX:41217487
|
CAT | C | 1 | a0001c0001t0001g0232 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6209+147_6209+148d others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chrX | 41217487 | |||||
| chrX:41217942
|
A | C | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.6210-430A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 36/44 | chrX | 41217942 | ||||||
| chrX:41218052
|
G | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.6210-320G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 36/44 | chrX | 41218052 | ||||||
| chrX:41218657
|
G | T | 1 | a0001c0001t0002g0087 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.6435+60G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 37/44 | chrX | 41218657 | ||||||
| chrX:41218890
|
AT | A | 1 | a0001c0001t0001g0006 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.6436-205delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 37/44 | INFO_REALIGN_3_PRIME | chrX | 41218890 | |||||
| chrX:41218969
|
ATAGTT | A | 1 | a0001c0001t0003g0285 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.6436-126_6436-122d others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 37/44 | INFO_REALIGN_3_PRIME | chrX | 41218969 | |||||
| chrX:41219028
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6436-74A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 37/44 | chrX | 41219028 | ||||||
| chrX:41219443
|
A | AT | 3 | a0001c0001t0001g0006a0002c0005t0011g0235a0002c0005t0011g0236 | 3 | HG06807.hp1 NA18981.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.6565+227dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | INFO_REALIGN_3_PRIME | chrX | 41219443 | |||||
| chrX:41219443
|
AT | A | 7 | a0001c0001t0001g0171a0001c0001t0001g0202a0001c0001t0001g0207others(4): Show | 7 | HG02723.hp2 HG02896.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.6565+227delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | INFO_REALIGN_3_PRIME | chrX | 41219443 | |||||
| chrX:41219638
|
A | G | 3 | a0001c0001t0004g0246a0001c0001t0004g0247a0001c0001t0004g0256 | 3 | NA18941.hp2 NA18975.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.6565+407A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41219638 | ||||||
| chrX:41220057
|
G | GT | 1 | a0006c0007t0020g0098 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.6565+834dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | INFO_REALIGN_3_PRIME | chrX | 41220057 | |||||
| chrX:41220063
|
T | C | 7 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(4): Show | 7 | HG01891.hp1 HG02895.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.6565+832T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41220063 | ||||||
| chrX:41220159
|
C | T | 3 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096 | 3 | HG02572.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.6565+928C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41220159 | ||||||
| chrX:41220494
|
A | G | 1 | a0001c0001t0003g0276 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6565+1263A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41220494 | ||||||
| chrX:41220511
|
T | C | 1 | a0001c0001t0003g0276 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6565+1280T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41220511 | ||||||
| chrX:41220924
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6565+1693A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41220924 | ||||||
| chrX:41220943
|
C | CA | 6 | a0001c0001t0001g0209a0001c0001t0002g0058a0001c0001t0002g0079others(3): Show | 6 | HG00621.hp1 HG02683.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.6565+1728dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | INFO_REALIGN_3_PRIME | chrX | 41220943 | |||||
| chrX:41220943
|
CA | C | 4 | a0001c0001t0001g0146a0001c0001t0004g0237a0001c0001t0004g0272others(1): Show | 4 | HG01256.hp1 HG03041.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.6565+1728delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | INFO_REALIGN_3_PRIME | chrX | 41220943 | |||||
| chrX:41221202
|
C | T | 1 | a0001c0001t0010g0156 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6565+1971C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41221202 | ||||||
| chrX:41221247
|
G | A | 2 | a0001c0001t0013g0180a0001c0001t0028g0179 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.6566-1970G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41221247 | ||||||
| chrX:41221248
|
C | T | 1 | a0001c0001t0030g0275 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.6566-1969C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41221248 | ||||||
| chrX:41221409
|
A | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.6566-1808A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41221409 | ||||||
| chrX:41221849
|
G | T | 1 | a0001c0001t0003g0288 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.6566-1368G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41221849 | ||||||
| chrX:41221889
|
CT | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.6566-1323delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | INFO_REALIGN_3_PRIME | chrX | 41221889 | |||||
| chrX:41222026
|
G | A | 1 | a0001c0001t0007g0020 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.6566-1191G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41222026 | ||||||
| chrX:41222077
|
A | T | 1 | a0001c0002t0002g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6566-1140A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41222077 | ||||||
| chrX:41222248
|
C | G | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(114): Show | 117 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.6566-969C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41222248 | ||||||
| chrX:41222287
|
C | CAAG | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.6566-929_6566-927d others(5): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | INFO_REALIGN_3_PRIME | chrX | 41222287 | |||||
| chrX:41222396
|
GA | G | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(114): Show | 117 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.6566-820delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41222396 | ||||||
| chrX:41222586
|
T | C | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.6566-631T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41222586 | ||||||
| chrX:41222650
|
G | T | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6566-567G>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41222650 | ||||||
| chrX:41222665
|
C | T | 1 | a0001c0001t0002g0100 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.6566-552C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41222665 | ||||||
| chrX:41222707
|
A | G | 1 | a0001c0001t0003g0239 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.6566-510A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41222707 | ||||||
| chrX:41222889
|
C | T | 3 | a0001c0001t0003g0259a0001c0001t0003g0274a0001c0001t0031g0273 | 3 | HG02523.hp1 NA19063.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.6566-328C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 38/44 | chrX | 41222889 | ||||||
| chrX:41223434
|
TTTTG | T | 2 | a0001c0001t0002g0028a0001c0001t0005g0054 | 2 | HG02451.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.6751+48_6751+51del others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 39/44 | INFO_REALIGN_3_PRIME | chrX | 41223434 | |||||
| chrX:41223528
|
C | T | 3 | a0001c0001t0005g0090a0001c0001t0005g0091a0001c0001t0005g0092 | 3 | HG02148.hp1 NA18973.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.6751+126C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 39/44 | chrX | 41223528 | ||||||
| chrX:41223592
|
C | T | 13 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(10): Show | 13 | HG00438.hp2 HG02074.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.6751+190C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 39/44 | chrX | 41223592 | ||||||
| chrX:41223983
|
T | G | 62 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(59): Show | 62 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.6751+581T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 39/44 | chrX | 41223983 | ||||||
| chrX:41224163
|
T | C | 62 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(59): Show | 62 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.6752-579T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 39/44 | chrX | 41224163 | ||||||
| chrX:41224487
|
T | G | 1 | a0001c0001t0002g0100 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.6752-255T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 39/44 | chrX | 41224487 | ||||||
| chrX:41224614
|
C | T | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(2): Show | 5 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.6752-128C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 39/44 | chrX | 41224614 | ||||||
| chrX:41224644
|
T | TA | 9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 9 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.6752-89dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 39/44 | INFO_REALIGN_3_PRIME | chrX | 41224644 | |||||
| chrX:41224707
|
A | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0213 | 2 | HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.6752-35A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 39/44 | chrX | 41224707 | ||||||
| chrX:41224724
|
G | C | 1 | a0004c0009t0006g0116 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.6752-18G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 39/44 | chrX | 41224724 | ||||||
| chrX:41225281
|
G | C | 31 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.7061+144G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41225281 | ||||||
| chrX:41225389
|
G | A | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.7061+252G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41225389 | ||||||
| chrX:41225554
|
C | T | 1 | a0001c0001t0004g0245 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.7061+417C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41225554 | ||||||
| chrX:41225900
|
A | G | 1 | a0001c0001t0002g0030 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.7061+763A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41225900 | ||||||
| chrX:41225932
|
A | T | 2 | a0001c0001t0002g0078a0001c0001t0002g0088 | 2 | NA18951.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.7061+795A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41225932 | ||||||
| chrX:41226027
|
G | A | 1 | a0001c0001t0003g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.7061+890G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41226027 | ||||||
| chrX:41226042
|
C | CT | 1 | a0001c0001t0007g0043 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.7061+907dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 41226042 | |||||
| chrX:41226082
|
A | C | 1 | a0001c0001t0003g0285 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.7061+945A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41226082 | ||||||
| chrX:41226111
|
G | GTTTAT | 7 | a0001c0001t0002g0046a0001c0001t0002g0087a0001c0001t0007g0017others(4): Show | 7 | HG00280.hp1 HG00733.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.7061+976_7061+977i others(7): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 41226111 | |||||
| chrX:41226118
|
A | C | 7 | a0001c0001t0002g0046a0001c0001t0002g0087a0001c0001t0007g0017others(4): Show | 7 | HG00280.hp1 HG00733.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.7061+981A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41226118 | ||||||
| chrX:41226119
|
T | TGC | 7 | a0001c0001t0002g0046a0001c0001t0002g0087a0001c0001t0007g0017others(4): Show | 7 | HG00280.hp1 HG00733.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.7061+982_7061+983i others(4): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41226119 | ||||||
| chrX:41226222
|
T | C | 1 | a0001c0001t0002g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.7061+1085T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41226222 | ||||||
| chrX:41226243
|
A | G | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.7061+1106A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41226243 | ||||||
| chrX:41226294
|
T | TG | 1 | a0001c0001t0001g0225 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.7061+1162dupG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 41226294 | |||||
| chrX:41226299
|
G | GT | 2 | a0001c0001t0002g0084a0001c0001t0008g0136 | 2 | HG01192.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.7061+1169dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 41226299 | |||||
| chrX:41226302
|
T | G | 1 | a0001c0001t0005g0051 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.7061+1165T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41226302 | ||||||
| chrX:41226363
|
A | T | 1 | a0001c0001t0004g0248 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.7061+1226A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41226363 | ||||||
| chrX:41226435
|
T | C | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.7061+1298T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41226435 | ||||||
| chrX:41226455
|
A | C | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.7061+1318A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41226455 | ||||||
| chrX:41226460
|
A | G | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.7061+1323A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41226460 | ||||||
| chrX:41226493
|
TAAAAC | T | 2 | a0001c0001t0002g0013a0001c0001t0022g0014 | 2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.7061+1360_7061+136 others(9): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 41226493 | |||||
| chrX:41226678
|
C | T | 1 | a0001c0001t0004g0260 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.7061+1541C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41226678 | ||||||
| chrX:41226715
|
G | A | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.7061+1578G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41226715 | ||||||
| chrX:41226757
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.7061+1620A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41226757 | ||||||
| chrX:41226773
|
C | T | 6 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0003t0001g0130others(3): Show | 6 | NA18954.hp2 NA18957.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.7061+1636C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41226773 | ||||||
| chrX:41226974
|
A | G | 2 | a0001c0001t0013g0180a0001c0001t0028g0179 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.7061+1837A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41226974 | ||||||
| chrX:41227049
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.7061+1912A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41227049 | ||||||
| chrX:41227112
|
A | C | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.7061+1975A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41227112 | ||||||
| chrX:41227114
|
T | C | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.7061+1977T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41227114 | ||||||
| chrX:41227131
|
C | T | 1 | a0007c0012t0001g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.7061+1994C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41227131 | ||||||
| chrX:41227378
|
T | C | 1 | a0001c0001t0005g0090 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.7062-1875T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41227378 | ||||||
| chrX:41227500
|
GA | G | 1 | a0001c0001t0001g0228 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.7062-1746delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 41227500 | |||||
| chrX:41227706
|
C | CT | 4 | a0001c0001t0002g0015a0001c0001t0002g0094a0001c0001t0002g0095others(1): Show | 4 | HG02572.hp1 HG02818.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.7062-1535dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 41227706 | |||||
| chrX:41227799
|
T | C | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.7062-1454T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41227799 | ||||||
| chrX:41228567
|
A | G | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.7062-686A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41228567 | ||||||
| chrX:41228577
|
T | C | 4 | a0001c0001t0001g0115a0001c0001t0001g0152a0001c0001t0001g0201others(1): Show | 4 | HG02027.hp1 HG02523.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.7062-676T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41228577 | ||||||
| chrX:41228625
|
A | AT | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.7062-627dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 41228625 | |||||
| chrX:41228725
|
AAGTT | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.7062-524_7062-521d others(6): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 41228725 | |||||
| chrX:41228863
|
A | AT | 1 | a0001c0001t0002g0050 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.7062-389dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 41228863 | |||||
| chrX:41228865
|
C | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.7062-388C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41228865 | ||||||
| chrX:41228884
|
G | A | 3 | a0001c0004t0002g0177a0001c0004t0002g0178a0001c0004t0002g0211 | 3 | HG02723.hp2 HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.7062-369G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41228884 | ||||||
| chrX:41228934
|
G | A | 1 | a0001c0001t0002g0034 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.7062-319G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41228934 | ||||||
| chrX:41228978
|
G | A | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.7062-275G>A | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41228978 | ||||||
| chrX:41229088
|
C | CA | 1 | a0001c0001t0019g0018 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.7062-157dupA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 41229088 | |||||
| chrX:41229096
|
A | T | 2 | a0001c0001t0001g0192a0001c0001t0025g0133 | 2 | HG03654.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.7062-157A>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 41/44 | chrX | 41229096 | ||||||
| chrX:41229971
|
C | T | 1 | a0001c0001t0005g0012 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.7431+192C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 43/44 | chrX | 41229971 | ||||||
| chrX:41230035
|
C | T | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.7431+256C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 43/44 | chrX | 41230035 | ||||||
| chrX:41230148
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.7432-353C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 43/44 | chrX | 41230148 | ||||||
| chrX:41230160
|
C | T | 4 | a0001c0003t0001g0130a0001c0003t0001g0150a0001c0003t0001g0151others(1): Show | 4 | NA18954.hp2 NA18957.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.7432-341C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 43/44 | chrX | 41230160 | ||||||
| chrX:41230199
|
C | G | 2 | a0001c0001t0013g0180a0001c0001t0028g0179 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.7432-302C>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 43/44 | chrX | 41230199 | ||||||
| chrX:41230335
|
TG | T | 1 | a0001c0001t0002g0083 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7432-165delG | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 43/44 | chrX | 41230335 | ||||||
| chrX:41230336
|
G | GT | 2 | a0001c0001t0003g0250a0001c0001t0004g0262 | 2 | HG01981.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.7432-151dupT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 43/44 | INFO_REALIGN_3_PRIME | chrX | 41230336 | |||||
| chrX:41230336
|
GT | G | 229 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0109others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.7432-151delT | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 43/44 | INFO_REALIGN_3_PRIME | chrX | 41230336 | |||||
| chrX:41230341
|
T | G | 4 | a0001c0001t0003g0238a0001c0001t0003g0243a0001c0001t0003g0244others(1): Show | 4 | HG01243.hp1 HG02145.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.7432-160T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 43/44 | chrX | 41230341 | ||||||
| chrX:41230348
|
T | G | 2 | a0002c0005t0011g0235a0002c0005t0011g0236 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.7432-153T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 43/44 | chrX | 41230348 | ||||||
| chrX:41230350
|
T | C | 2 | a0001c0002t0002g0121a0001c0002t0002g0122 | 2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.7432-151T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 43/44 | chrX | 41230350 | ||||||
| chrX:41230718
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.7527+122T>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 44/44 | chrX | 41230718 | ||||||
| chrX:41231046
|
A | C | 2 | a0001c0001t0003g0284a0001c0001t0003g0290 | 2 | HG03669.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.7527+450A>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 44/44 | chrX | 41231046 | ||||||
| chrX:41231158
|
T | G | 139 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(136): Show | 139 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.7527+562T>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 44/44 | chrX | 41231158 | ||||||
| chrX:41231206
|
G | C | 58 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(55): Show | 58 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.7527+610G>C | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 44/44 | chrX | 41231206 | ||||||
| chrX:41231230
|
C | T | 1 | a0001c0002t0021g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.7527+634C>T | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 44/44 | chrX | 41231230 | ||||||
| chrX:41231731
|
CA | C | 14 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0223others(11): Show | 14 | HG01074.hp1 HG01167.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.7528-638delA | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chrX | 41231731 | |||||
| chrX:41231938
|
A | G | 56 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.7528-449A>G | USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 44/44 | chrX | 41231938 | ||||||
| chrX:41232219
|
T | TTTTTTG | 288 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.7528-145_7528-140d others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chrX | 41232219 | |||||
| chrX:41232219
|
T | TTTTTTGT others(5): Show |
1 | a0001c0001t0003g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7528-151_7528-140d others(14): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chrX | 41232219 | |||||
| chrX:41232219
|
TTTTTTG | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0213 | 2 | HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.7528-145_7528-140d others(8): Show |
USP9X | ENSG00000124486.15 | transcript | ENST00000378308.7 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chrX | 41232219 |