Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4267 |
|---|---|
| ensemblid | ENSG00000002586.20 |
| hgncid | 7082 |
| symbol | CD99 |
| name | CD99 molecule (Xg blood group) |
| refseq_nuc | NM_002414.5 |
| refseq_prot | NP_002405.1 |
| ensembl_nuc | ENST00000381192.10 |
| ensembl_prot | ENSP00000370588.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 2691295 |
| end | 2741309 |
| strand | + |
| ver | v1.2 |
| region | chrX:2691295-2741309 |
| region5000 | chrX:2686295-2746309 |
| regionname0 | CD99_chrX_2691295_2741309 |
| regionname5000 | CD99_chrX_2686295_2746309 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 185 | 202 | 52 | 37 | 90 | 7 | 14 | 69 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0002 | 0/0 | 185 | 15 | 4 | 5 | 3 | 0 | 3 | 3 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0003 | 0/0 | 185 | 6 | 4 | 2 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0004 | 0/0 | 185 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0005 | 0/0 | 29 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0006 | 0/0 | 182 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0007 | 0/0 | 185 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 558 | 123 | 46 | 13 | 52 | 3 | 7 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| c0002 | 0/0 | 558 | 58 | 0 | 16 | 31 | 4 | 7 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| c0003 | 0/0 | 558 | 11 | 4 | 3 | 2 | 0 | 2 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| c0004 | 0/0 | 558 | 9 | 3 | 6 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| c0005 | 0/0 | 558 | 5 | 0 | 0 | 5 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| c0006 | 0/0 | 558 | 5 | 1 | 2 | 2 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| c0007 | 0/0 | 558 | 4 | 0 | 2 | 1 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| c0008 | 0/0 | 558 | 4 | 4 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| c0009 | 0/0 | 558 | 2 | 0 | 2 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| c0010 | 0/0 | 559 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| c0011 | 0/0 | 558 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| c0012 | 0/0 | 558 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| c0013 | 0/0 | 557 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| c0014 | 0/0 | 558 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| c0015 | 0/0 | 558 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| c0016 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 572 | 188 | 45 | 38 | 81 | 6 | 16 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| t0002 | 0/0 | 573 | 19 | 5 | 4 | 8 | 1 | 1 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| t0003 | 0/0 | 572 | 5 | 0 | 2 | 3 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| t0004 | 0/0 | 572 | 4 | 4 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| t0005 | 0/0 | 572 | 3 | 3 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| t0006 | 0/0 | 572 | 2 | 2 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| t0007 | 0/0 | 572 | 2 | 1 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| t0008 | 0/0 | 571 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| t0009 | 0/0 | 573 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| t0010 | 0/0 | 572 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| t0011 | 0/0 | 572 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| t0012 | 0/0 | 573 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 558 | 123 | 46 | 13 | 52 | 3 | 7 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0002 | 0/0 | 558 | 58 | 0 | 16 | 31 | 4 | 7 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0004 | 0/0 | 558 | 9 | 3 | 6 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0005 | 0/0 | 558 | 5 | 0 | 0 | 5 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0006 | 0/0 | 558 | 5 | 1 | 2 | 2 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0011 | 0/0 | 558 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0014 | 0/0 | 558 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0002c0003 | 0/0 | 558 | 11 | 4 | 3 | 2 | 0 | 2 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0002c0007 | 0/0 | 558 | 4 | 0 | 2 | 1 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0003c0008 | 0/0 | 558 | 4 | 4 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0003c0009 | 0/0 | 558 | 2 | 0 | 2 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0004c0012 | 0/0 | 558 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0004c0015 | 0/0 | 558 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0005c0010 | 0/0 | 559 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0006c0013 | 0/0 | 557 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0007c0016 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1129 | 98 | 36 | 9 | 42 | 3 | 6 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0001t0002 | 0/0 | 1130 | 14 | 4 | 2 | 7 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0001t0003 | 0/0 | 1129 | 3 | 0 | 2 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0001t0005 | 0/0 | 1129 | 3 | 3 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0001t0006 | 0/0 | 1129 | 2 | 2 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0001t0009 | 0/0 | 1130 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0001t0011 | 0/0 | 1129 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0001t0012 | 0/0 | 1130 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0002t0001 | 0/0 | 1129 | 53 | 0 | 16 | 27 | 3 | 7 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0002t0002 | 0/0 | 1130 | 2 | 0 | 0 | 1 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0002t0003 | 0/0 | 1129 | 2 | 0 | 0 | 2 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0002t0010 | 0/0 | 1129 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0004t0001 | 0/0 | 1129 | 7 | 2 | 5 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0004t0002 | 0/0 | 1130 | 2 | 1 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0005t0001 | 0/0 | 1129 | 5 | 0 | 0 | 5 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0006t0001 | 0/0 | 1129 | 4 | 1 | 1 | 2 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0006t0002 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0011t0001 | 0/0 | 1129 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0001c0014t0001 | 0/0 | 1129 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0002c0003t0001 | 0/0 | 1129 | 11 | 4 | 3 | 2 | 0 | 2 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0002c0007t0001 | 0/0 | 1129 | 4 | 0 | 2 | 1 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0003c0008t0004 | 0/0 | 1129 | 4 | 4 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0003c0009t0001 | 0/0 | 1129 | 2 | 0 | 2 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0004c0012t0007 | 0/0 | 1129 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0004c0015t0007 | 0/0 | 1129 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0005c0010t0001 | 0/0 | 1130 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0006c0013t0008 | 0/0 | 1127 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| a0007c0016t0001 | 0/0 | 1129 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | copy fasta | chrX | 2686295 | 2746309 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0009g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0011g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0001t0012g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0002t0010g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0004t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0004t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0004t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0004t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0004t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0004t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0004t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0004t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0004t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0005t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0005t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0005t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0005t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0005t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0006t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0006t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0006t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0006t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0006t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0011t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0001c0014t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0003t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0007t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0007t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0007t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0002c0007t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0003c0008t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0003c0008t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0003c0008t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0003c0008t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0003c0009t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0003c0009t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0004c0012t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0004c0015t0007g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0005c0010t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0006c0013t0008g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| a0007c0016t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0047 | EUR | GBR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | GBR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0188 | EUR | FIN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0121 | EUR | FIN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00408 | hp1 | a0001 | c0002 | t0010 | g0135 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00544 | hp1 | a0001 | c0005 | t0001 | g0210 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | CHS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00639 | hp1 | a0002 | c0007 | t0001 | g0020 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01168 | hp1 | a0001 | c0006 | t0001 | g0201 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01168 | hp2 | a0003 | c0009 | t0001 | g0191 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01169 | hp1 | a0003 | c0009 | t0001 | g0190 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01175 | hp2 | a0001 | c0004 | t0001 | g0145 | AMR | PUR | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01257 | hp2 | a0001 | c0006 | t0002 | g0164 | AMR | CLM | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | CLM | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01346 | hp2 | a0001 | c0004 | t0001 | g0146 | AMR | CLM | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01496 | hp1 | a0002 | c0003 | t0001 | g0211 | AMR | CLM | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0036 | AMR | CLM | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01516 | hp2 | a0004 | c0015 | t0007 | g0018 | EUR | IBS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0025 | EUR | IBS | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01884 | hp1 | a0001 | c0004 | t0002 | g0082 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0196 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0125 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0144 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0160 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0163 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01981 | hp2 | a0002 | c0003 | t0001 | g0208 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01993 | hp2 | a0002 | c0003 | t0001 | g0151 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02004 | hp1 | a0001 | c0004 | t0002 | g0035 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02004 | hp2 | a0002 | c0007 | t0001 | g0022 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0126 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02148 | hp2 | a0001 | c0004 | t0001 | g0143 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CDX | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CDX | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | CDX | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0064 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02273 | hp1 | a0001 | c0004 | t0001 | g0142 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0048 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02293 | hp1 | a0001 | c0004 | t0001 | g0015 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0128 | AMR | PEL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | KHV | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02615 | hp1 | a0002 | c0003 | t0001 | g0221 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02622 | hp1 | a0002 | c0003 | t0001 | g0222 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0027 | SAS | PJL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0149 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02896 | hp1 | a0003 | c0008 | t0004 | g0087 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02896 | hp2 | a0002 | c0003 | t0001 | g0203 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02897 | hp2 | a0003 | c0008 | t0004 | g0088 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | ESN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0223 | AFR | ESN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03486 | hp1 | a0003 | c0008 | t0004 | g0089 | AFR | MSL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03486 | hp2 | a0001 | c0014 | t0001 | g0193 | AFR | MSL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0171 | AFR | ESN | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03540 | hp1 | a0004 | c0012 | t0007 | g0013 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03669 | hp2 | a0002 | c0003 | t0001 | g0099 | SAS | PJL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0045 | SAS | PJL | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03831 | hp1 | a0002 | c0007 | t0001 | g0028 | SAS | BEB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0199 | SAS | BEB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0123 | SAS | BEB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0029 | SAS | BEB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0166 | SAS | BEB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18906 | hp1 | a0003 | c0008 | t0004 | g0071 | AFR | YRI | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18941 | hp1 | a0001 | c0002 | t0003 | g0114 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18950 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18969 | hp2 | a0001 | c0002 | t0003 | g0113 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18974 | hp1 | a0002 | c0007 | t0001 | g0112 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18975 | hp1 | a0001 | c0006 | t0001 | g0055 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18992 | hp1 | a0006 | c0013 | t0008 | g0012 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19001 | hp2 | a0005 | c0010 | t0001 | g0165 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19002 | hp2 | a0001 | c0005 | t0001 | g0219 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19006 | hp1 | a0001 | c0005 | t0001 | g0129 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19030 | hp1 | a0002 | c0003 | t0001 | g0005 | AFR | LWK | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19064 | hp1 | a0001 | c0005 | t0001 | g0131 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19076 | hp2 | a0001 | c0001 | t0011 | g0176 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19077 | hp1 | a0001 | c0001 | t0012 | g0207 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19077 | hp2 | a0007 | c0016 | t0001 | g0132 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19080 | hp1 | a0001 | c0006 | t0001 | g0140 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19084 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19087 | hp1 | a0001 | c0005 | t0001 | g0130 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0093 | AFR | YRI | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | YRI | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ASW | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0042 | SAS | GIH | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0127 | AMR | CLM | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | USA | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0220 | AFR | USA | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | USA | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA21309 | hp1 | a0001 | c0011 | t0001 | g0202 | AFR | LWK | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| NA21309 | hp2 | a0001 | c0006 | t0001 | g0040 | AFR | LWK | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0067 | REF | REF | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0168 | REF | REF | CD99_chrX_2686295_2746309 | CD99 | chrX | 2686295 | 2746309 |
| 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:2691364
|
G | GC | 1 | a0005 | 1 | NA19001.hp2 | frameshift_variant | HIGH | c.7dupC | p.Arg3fs | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/10 | 74/1129 | 8/558 | 3/185 | INFO_REALIGN_3_PRIME | chrX | 2691364 | |
| chrX:2691412
|
C | G | 1 | a0003 | 6 | HG01168.hp2 HG01169.hp1 HG02896.hp1 others(3): Show |
missense_variant | MODERATE | c.52C>G | p.Leu18Val | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/10 | 118/1129 | 52/558 | 18/185 | chrX | 2691412 | ||
| chrX:2714422
|
A | G | 1 | a0007 | 1 | NA19077.hp2 | missense_variant&splice_region_variant | MODERATE | c.68A>G | p.Asp23Gly | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/10 | 134/1129 | 68/558 | 23/185 | chrX | 2714422 | ||
| chrX:2738217
|
G | A | 1 | a0004 | 2 | HG01516.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.493G>A | p.Asp165Asn | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/10 | 559/1129 | 493/558 | 165/185 | chrX | 2738217 | ||
| chrX:2738220
|
A | G | 3 | a0002a0005a0007 | 17 | HG00639.hp1 HG01496.hp1 HG01981.hp2 others(14): Show |
missense_variant | MODERATE | c.496A>G | p.Met166Val | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/10 | 562/1129 | 496/558 | 166/185 | chrX | 2738220 | ||
| chrX:2738242
|
A | T | 3 | a0002a0005a0007 | 17 | HG00639.hp1 HG01496.hp1 HG01981.hp2 others(14): Show |
missense_variant | MODERATE | c.518A>T | p.Asn173Ile | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/10 | 584/1129 | 518/558 | 173/185 | chrX | 2738242 | ||
| chrX:2740790
|
CT | C | 1 | a0006 | 1 | NA18992.hp1 | frameshift_variant | HIGH | c.548delT | p.Leu183fs | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 614/1129 | 548/558 | 183/185 | INFO_REALIGN_3_PRIME | chrX | 2740790 |
| 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:2714441
|
C | T | 6 | a0001c0002a0001c0006a0002c0007others(3): Show | 70 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
synonymous_variant | LOW | c.87C>T | p.Ser29Ser | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/10 | 153/1129 | 87/558 | 29/185 | chrX | 2714441 | ||
| chrX:2722652
|
G | A | 1 | a0001c0011 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.288G>A | p.Ala96Ala | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/10 | 354/1129 | 288/558 | 96/185 | chrX | 2722652 | ||
| chrX:2726261
|
C | T | 4 | a0001c0004a0001c0006a0001c0011others(1): Show | 17 | HG01168.hp1 HG01168.hp2 HG01169.hp1 others(14): Show |
splice_region_variant&synonymous_variant | LOW | c.363C>T | p.Ala121Ala | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/10 | 429/1129 | 363/558 | 121/185 | chrX | 2726261 | ||
| chrX:2726273
|
C | T | 1 | a0001c0014 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.375C>T | p.Gly125Gly | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/10 | 441/1129 | 375/558 | 125/185 | chrX | 2726273 | ||
| chrX:2726282
|
C | T | 1 | a0001c0005 | 5 | HG00544.hp1 NA19002.hp2 NA19006.hp1 others(2): Show |
synonymous_variant | LOW | c.384C>T | p.Pro128Pro | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/10 | 450/1129 | 384/558 | 128/185 | chrX | 2726282 |
| 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:2691310
|
T | A | 1 | a0003c0008t0004 | 4 | HG02896.hp1 HG02897.hp2 HG03486.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-51T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/10 | 51 | chrX | 2691310 | |||||
| chrX:2740863
|
G | GC | 1 | a0006c0013t0008 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*60dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 61 | INFO_REALIGN_3_PRIME | chrX | 2740863 | ||||
| chrX:2740892
|
G | GGC | 1 | a0006c0013t0008 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*88_*89insGC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 89 | chrX | 2740892 | |||||
| chrX:2740893
|
C | A | 1 | a0006c0013t0008 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*89C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 89 | chrX | 2740893 | |||||
| chrX:2740979
|
T | TA | 1 | a0006c0013t0008 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*177dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 178 | INFO_REALIGN_3_PRIME | chrX | 2740979 | ||||
| chrX:2741001
|
AG | A | 1 | a0006c0013t0008 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*202delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 202 | INFO_REALIGN_3_PRIME | chrX | 2741001 | ||||
| chrX:2741006
|
G | GA | 1 | a0001c0001t0009 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*203dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 204 | INFO_REALIGN_3_PRIME | chrX | 2741006 | ||||
| chrX:2741035
|
GC | G | 1 | a0006c0013t0008 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*234delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 234 | INFO_REALIGN_3_PRIME | chrX | 2741035 | ||||
| chrX:2741038
|
C | CG | 1 | a0001c0001t0012 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*241dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 242 | INFO_REALIGN_3_PRIME | chrX | 2741038 | ||||
| chrX:2741046
|
CG | C | 1 | a0006c0013t0008 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*244delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 244 | INFO_REALIGN_3_PRIME | chrX | 2741046 | ||||
| chrX:2741113
|
G | A | 2 | a0001c0001t0003a0001c0002t0003 | 5 | HG01978.hp1 HG01981.hp1 NA18941.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*309G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 309 | chrX | 2741113 | |||||
| chrX:2741118
|
A | AC | 4 | a0001c0001t0002a0001c0002t0002a0001c0004t0002others(1): Show | 19 | HG01070.hp1 HG01071.hp2 HG01257.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*321dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 322 | INFO_REALIGN_3_PRIME | chrX | 2741118 | ||||
| chrX:2741118
|
AC | A | 1 | a0006c0013t0008 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*321delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 321 | INFO_REALIGN_3_PRIME | chrX | 2741118 | ||||
| chrX:2741164
|
A | T | 1 | a0001c0001t0005 | 3 | HG02976.hp1 HG03195.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*360A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 360 | chrX | 2741164 | |||||
| chrX:2741184
|
C | G | 1 | a0001c0001t0011 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*380C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 380 | chrX | 2741184 | |||||
| chrX:2741187
|
G | C | 1 | a0001c0001t0006 | 2 | HG01891.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*383G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 383 | chrX | 2741187 | |||||
| chrX:2741191
|
C | T | 2 | a0004c0012t0007a0004c0015t0007 | 2 | HG01516.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*387C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 387 | chrX | 2741191 | |||||
| chrX:2741194
|
C | T | 1 | a0001c0002t0010 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*390C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 390 | chrX | 2741194 | |||||
| chrX:2741203
|
T | C | 1 | a0006c0013t0008 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*399T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 399 | chrX | 2741203 | |||||
| chrX:2741214
|
TA | T | 1 | a0006c0013t0008 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*412delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 10/10 | 412 | INFO_REALIGN_3_PRIME | chrX | 2741214 |
| 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:2691452
|
T | TG | 1 | a0001c0001t0002g0224 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.67+30dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2691452 | |||||
| chrX:2691457
|
G | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG06807.hp2 NA18906.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+30G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691457 | ||||||
| chrX:2691502
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | HG00438.hp2 HG00733.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+75G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691502 | ||||||
| chrX:2691510
|
G | C | 1 | a0001c0001t0001g0014 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67+83G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691510 | ||||||
| chrX:2691568
|
C | CG | 1 | a0001c0001t0002g0224 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.67+146dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2691568 | |||||
| chrX:2691676
|
G | T | 58 | a0001c0001t0001g0014a0001c0001t0001g0169a0001c0001t0001g0170others(55): Show | 59 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.67+249G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691676 | ||||||
| chrX:2691708
|
T | C | 171 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(168): Show | 174 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.67+281T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691708 | ||||||
| chrX:2691824
|
G | C | 1 | a0001c0001t0001g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.67+397G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691824 | ||||||
| chrX:2691824
|
G | T | 1 | a0001c0002t0002g0167 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.67+397G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691824 | ||||||
| chrX:2691825
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.67+398C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691825 | ||||||
| chrX:2691840
|
C | A | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.67+413C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691840 | ||||||
| chrX:2691886
|
A | G | 1 | a0001c0002t0001g0166 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.67+459A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691886 | ||||||
| chrX:2691904
|
TG | T | 1 | a0005c0010t0001g0165 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.67+479delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2691904 | |||||
| chrX:2691918
|
G | C | 1 | a0001c0004t0001g0015 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.67+491G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691918 | ||||||
| chrX:2691942
|
T | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(80): Show | 84 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.67+515T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691942 | ||||||
| chrX:2691984
|
C | T | 61 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0133others(58): Show | 63 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.67+557C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2691984 | ||||||
| chrX:2692021
|
G | C | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0175 | 3 | HG02257.hp2 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.67+594G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692021 | ||||||
| chrX:2692111
|
GC | G | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.67+686delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2692111 | |||||
| chrX:2692120
|
ACCCTCCC others(4): Show |
A | 1 | a0001c0001t0001g0080 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.67+696_67+706delCT others(9): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2692120 | |||||
| chrX:2692183
|
C | T | 5 | a0001c0001t0001g0081a0001c0001t0001g0104a0001c0001t0001g0105others(2): Show | 5 | HG00423.hp1 HG02080.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+756C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692183 | ||||||
| chrX:2692212
|
GC | G | 1 | a0001c0006t0002g0164 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.67+787delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2692212 | |||||
| chrX:2692221
|
G | A | 14 | a0001c0001t0001g0014a0001c0001t0001g0177a0001c0001t0001g0178others(11): Show | 14 | HG02080.hp1 HG02155.hp1 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+794G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692221 | ||||||
| chrX:2692243
|
CATGTTAT others(12): Show |
C | 58 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(55): Show | 59 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.67+817_67+835delAT others(17): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692243 | ||||||
| chrX:2692265
|
A | G | 58 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(55): Show | 59 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.67+838A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692265 | ||||||
| chrX:2692393
|
G | T | 2 | a0001c0001t0002g0033a0001c0001t0005g0034 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.67+966G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692393 | ||||||
| chrX:2692453
|
T | G | 25 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0107others(22): Show | 25 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.67+1026T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692453 | ||||||
| chrX:2692470
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.67+1043G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692470 | ||||||
| chrX:2692634
|
C | G | 8 | a0001c0001t0001g0100a0001c0001t0001g0169a0001c0001t0001g0170others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+1207C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692634 | ||||||
| chrX:2692668
|
G | GTCCT | 71 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(68): Show | 72 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.67+1244_67+1247dup others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2692668 | |||||
| chrX:2692788
|
A | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0005g0223 | 3 | HG02257.hp2 HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.67+1361A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692788 | ||||||
| chrX:2692803
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.67+1376A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692803 | ||||||
| chrX:2692836
|
G | T | 2 | a0001c0001t0002g0033a0001c0001t0005g0034 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.67+1409G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692836 | ||||||
| chrX:2692864
|
G | A | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 4 | HG03195.hp1 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+1437G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692864 | ||||||
| chrX:2692942
|
G | A | 2 | a0001c0001t0002g0033a0001c0001t0005g0034 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.67+1515G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2692942 | ||||||
| chrX:2693050
|
G | C | 3 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0004t0002g0035 | 3 | HG01496.hp2 HG01993.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.67+1623G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693050 | ||||||
| chrX:2693111
|
A | G | 52 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0083others(49): Show | 54 | HG00408.hp1 HG00544.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.67+1684A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693111 | ||||||
| chrX:2693141
|
G | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(46): Show | 50 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.67+1714G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693141 | ||||||
| chrX:2693150
|
G | GT | 3 | a0001c0001t0001g0175a0001c0001t0001g0187a0002c0003t0001g0221 | 3 | HG02615.hp1 HG02922.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.67+1735dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2693150 | |||||
| chrX:2693150
|
G | GTGGT | 2 | a0001c0001t0002g0033a0001c0001t0005g0034 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.67+1724_67+1725ins others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2693150 | |||||
| chrX:2693150
|
G | GTGGTT | 44 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0083others(41): Show | 46 | HG00408.hp1 HG00544.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.67+1724_67+1725ins others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2693150 | |||||
| chrX:2693150
|
G | GTGGTTT | 6 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0003g0163others(3): Show | 6 | HG01884.hp1 HG01981.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+1724_67+1725ins others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2693150 | |||||
| chrX:2693150
|
G | GTT | 1 | a0002c0003t0001g0222 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.67+1734_67+1735dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2693150 | |||||
| chrX:2693150
|
GT | G | 1 | a0003c0008t0004g0087 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.67+1735delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2693150 | |||||
| chrX:2693158
|
T | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(46): Show | 50 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.67+1731T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693158 | ||||||
| chrX:2693204
|
A | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(98): Show | 104 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.67+1777A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693204 | ||||||
| chrX:2693372
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.67+1945A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693372 | ||||||
| chrX:2693395
|
A | G | 3 | a0001c0001t0001g0174a0001c0001t0002g0033a0001c0001t0005g0034 | 3 | HG02615.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.67+1968A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693395 | ||||||
| chrX:2693410
|
G | C | 57 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0083others(54): Show | 59 | HG00408.hp1 HG00544.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.67+1983G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693410 | ||||||
| chrX:2693458
|
C | G | 54 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0083others(51): Show | 56 | HG00408.hp1 HG00544.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.67+2031C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693458 | ||||||
| chrX:2693594
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0170others(3): Show | 6 | HG02257.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+2167G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693594 | ||||||
| chrX:2693659
|
G | A | 1 | a0007c0016t0001g0132 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.67+2232G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693659 | ||||||
| chrX:2693670
|
G | C | 3 | a0001c0001t0001g0004a0001c0001t0002g0098a0002c0003t0001g0005 | 3 | HG02723.hp2 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.67+2243G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693670 | ||||||
| chrX:2693749
|
A | T | 1 | a0002c0007t0001g0028 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.67+2322A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693749 | ||||||
| chrX:2693855
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.67+2428G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693855 | ||||||
| chrX:2693871
|
A | AC | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.67+2447dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2693871 | |||||
| chrX:2693947
|
C | G | 9 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0170others(6): Show | 9 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+2520C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2693947 | ||||||
| chrX:2694008
|
A | G | 1 | a0004c0012t0007g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.67+2581A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2694008 | ||||||
| chrX:2694020
|
AG | A | 1 | a0001c0001t0001g0080 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.67+2596delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2694020 | |||||
| chrX:2694089
|
A | G | 8 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0175others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+2662A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2694089 | ||||||
| chrX:2694146
|
A | AC | 1 | a0001c0001t0001g0080 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.67+2725dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2694146 | |||||
| chrX:2694266
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0170 | 2 | HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.67+2839T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2694266 | ||||||
| chrX:2694279
|
G | GT | 19 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073others(16): Show | 19 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.67+2867dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2694279 | |||||
| chrX:2694279
|
GT | G | 1 | a0003c0009t0001g0190 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.67+2867delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2694279 | |||||
| chrX:2694295
|
A | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0170others(1): Show | 4 | HG02080.hp2 HG02257.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+2868A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2694295 | ||||||
| chrX:2694362
|
TG | T | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.67+2938delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2694362 | |||||
| chrX:2694482
|
G | T | 1 | a0001c0001t0005g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.67+3055G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2694482 | ||||||
| chrX:2694511
|
A | AG | 1 | a0001c0001t0001g0080 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.67+3085dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2694511 | |||||
| chrX:2694519
|
AG | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(146): Show | 152 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.67+3095delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2694519 | |||||
| chrX:2694618
|
T | TG | 1 | a0001c0001t0001g0080 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.67+3193dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2694618 | |||||
| chrX:2694677
|
C | CG | 1 | a0001c0001t0001g0080 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.67+3253dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2694677 | |||||
| chrX:2694688
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0002g0098 | 3 | HG02622.hp2 HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.67+3261G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2694688 | ||||||
| chrX:2694753
|
A | C | 55 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(52): Show | 56 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+3326A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2694753 | ||||||
| chrX:2694756
|
G | GA | 5 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0188others(2): Show | 5 | HG00323.hp1 HG00639.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+3340dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2694756 | |||||
| chrX:2694756
|
GA | G | 1 | a0001c0001t0001g0159 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.67+3340delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2694756 | |||||
| chrX:2694886
|
AT | A | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.67+3464delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2694886 | |||||
| chrX:2694908
|
T | C | 2 | a0001c0001t0002g0085a0001c0001t0002g0086 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.67+3481T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2694908 | ||||||
| chrX:2695018
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.67+3591C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695018 | ||||||
| chrX:2695064
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.67+3637C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695064 | ||||||
| chrX:2695188
|
T | C | 1 | a0001c0001t0001g0007 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.67+3761T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695188 | ||||||
| chrX:2695191
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0005g0093 | 3 | HG02630.hp2 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.67+3764C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695191 | ||||||
| chrX:2695213
|
C | CT | 8 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(5): Show | 8 | HG02622.hp2 HG02723.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+3796dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2695213 | |||||
| chrX:2695213
|
CT | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0200 | 2 | NA18989.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.67+3796delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2695213 | |||||
| chrX:2695238
|
C | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(50): Show | 54 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.67+3811C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695238 | ||||||
| chrX:2695409
|
T | G | 1 | a0001c0002t0001g0134 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.67+3982T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695409 | ||||||
| chrX:2695521
|
T | C | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+4094T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695521 | ||||||
| chrX:2695535
|
T | C | 161 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(158): Show | 164 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.67+4108T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695535 | ||||||
| chrX:2695552
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(5): Show | 8 | HG02257.hp2 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+4125C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695552 | ||||||
| chrX:2695554
|
A | G | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+4127A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695554 | ||||||
| chrX:2695585
|
AT | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG00741.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.67+4165delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2695585 | |||||
| chrX:2695588
|
T | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG00741.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.67+4161T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695588 | ||||||
| chrX:2695637
|
C | CT | 20 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0038others(17): Show | 20 | HG01891.hp1 HG01975.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.67+4224dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2695637 | |||||
| chrX:2695637
|
C | CTT | 41 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(38): Show | 42 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.67+4223_67+4224dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2695637 | |||||
| chrX:2695637
|
C | CTTT | 2 | a0001c0001t0001g0070a0001c0001t0001g0080 | 2 | HG00423.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.67+4222_67+4224dup others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2695637 | |||||
| chrX:2695637
|
CT | C | 2 | a0001c0001t0011g0176a0001c0006t0002g0164 | 2 | HG01257.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.67+4224delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2695637 | |||||
| chrX:2695638
|
T | C | 2 | a0001c0001t0002g0033a0001c0001t0005g0034 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.67+4211T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695638 | ||||||
| chrX:2695659
|
T | A | 166 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(163): Show | 169 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.67+4232T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695659 | ||||||
| chrX:2695712
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.67+4285C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695712 | ||||||
| chrX:2695713
|
G | A | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+4286G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695713 | ||||||
| chrX:2695822
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0002g0098 | 3 | HG02622.hp2 HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.67+4395C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695822 | ||||||
| chrX:2695877
|
G | A | 9 | a0001c0001t0001g0006a0001c0001t0001g0172a0001c0001t0001g0173others(6): Show | 9 | HG01891.hp1 HG02451.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+4450G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695877 | ||||||
| chrX:2695956
|
A | G | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+4529A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695956 | ||||||
| chrX:2695971
|
T | C | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+4544T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2695971 | ||||||
| chrX:2696022
|
C | T | 1 | a0001c0014t0001g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.67+4595C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696022 | ||||||
| chrX:2696041
|
A | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.67+4614A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696041 | ||||||
| chrX:2696071
|
G | A | 26 | a0001c0001t0001g0026a0001c0001t0001g0044a0001c0002t0001g0008others(23): Show | 26 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.67+4644G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696071 | ||||||
| chrX:2696121
|
AT | A | 1 | a0001c0001t0001g0080 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.67+4699delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2696121 | |||||
| chrX:2696145
|
G | C | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+4718G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696145 | ||||||
| chrX:2696178
|
A | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(85): Show | 89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.67+4751A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696178 | ||||||
| chrX:2696198
|
G | C | 1 | a0002c0007t0001g0028 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.67+4771G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696198 | ||||||
| chrX:2696226
|
T | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(47): Show | 51 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.67+4799T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696226 | ||||||
| chrX:2696228
|
T | TG | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+4802dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2696228 | |||||
| chrX:2696264
|
T | TC | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+4838dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2696264 | |||||
| chrX:2696267
|
TC | T | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+4842delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2696267 | |||||
| chrX:2696269
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0170 | 2 | HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.67+4842C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696269 | ||||||
| chrX:2696294
|
TG | T | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.67+4871delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2696294 | |||||
| chrX:2696309
|
C | T | 1 | a0001c0006t0001g0040 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.67+4882C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696309 | ||||||
| chrX:2696393
|
CTTTCT | C | 5 | a0001c0001t0001g0069a0001c0001t0001g0106a0001c0001t0001g0155others(2): Show | 5 | HG00544.hp2 HG01891.hp2 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+4980_67+4984del others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2696393 | |||||
| chrX:2696439
|
T | C | 161 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(158): Show | 164 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.67+5012T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696439 | ||||||
| chrX:2696547
|
C | T | 5 | a0001c0001t0001g0069a0001c0001t0001g0106a0001c0001t0001g0155others(2): Show | 5 | HG00544.hp2 HG01891.hp2 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+5120C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696547 | ||||||
| chrX:2696557
|
C | A | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+5130C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696557 | ||||||
| chrX:2696558
|
A | G | 5 | a0001c0001t0001g0069a0001c0001t0001g0106a0001c0001t0001g0155others(2): Show | 5 | HG00544.hp2 HG01891.hp2 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+5131A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696558 | ||||||
| chrX:2696575
|
AT | A | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+5155delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2696575 | |||||
| chrX:2696649
|
C | T | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+5222C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696649 | ||||||
| chrX:2696673
|
CT | C | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+5252delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2696673 | |||||
| chrX:2696927
|
T | G | 3 | a0001c0001t0001g0175a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | HG01070.hp1 HG01071.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.67+5500T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2696927 | ||||||
| chrX:2697031
|
T | C | 5 | a0001c0001t0001g0069a0001c0001t0001g0106a0001c0001t0001g0155others(2): Show | 5 | HG00544.hp2 HG01891.hp2 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+5604T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697031 | ||||||
| chrX:2697142
|
C | T | 1 | a0002c0003t0001g0099 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.67+5715C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697142 | ||||||
| chrX:2697145
|
T | TC | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+5721dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2697145 | |||||
| chrX:2697153
|
TC | T | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.67+5729delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2697153 | |||||
| chrX:2697156
|
C | T | 5 | a0001c0001t0001g0069a0001c0001t0001g0106a0001c0001t0001g0155others(2): Show | 5 | HG00544.hp2 HG01891.hp2 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+5729C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697156 | ||||||
| chrX:2697206
|
TG | T | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+5781delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2697206 | |||||
| chrX:2697312
|
A | C | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+5885A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697312 | ||||||
| chrX:2697338
|
C | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(35): Show | 39 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.67+5911C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697338 | ||||||
| chrX:2697352
|
GT | G | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+5927delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2697352 | |||||
| chrX:2697464
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67+6037C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697464 | ||||||
| chrX:2697475
|
T | C | 149 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(146): Show | 152 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.67+6048T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697475 | ||||||
| chrX:2697482
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(36): Show | 40 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.67+6055A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697482 | ||||||
| chrX:2697555
|
C | A | 95 | a0001c0001t0001g0044a0001c0001t0001g0072a0001c0001t0001g0073others(92): Show | 97 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.67+6128C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697555 | ||||||
| chrX:2697946
|
T | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(140): Show | 146 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.67+6519T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2697946 | ||||||
| chrX:2697996
|
T | TG | 1 | a0001c0001t0001g0026 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.67+6570dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2697996 | |||||
| chrX:2698084
|
TG | T | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.67+6660delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2698084 | |||||
| chrX:2698185
|
C | CT | 4 | a0001c0001t0001g0187a0001c0001t0002g0184a0001c0001t0003g0152others(1): Show | 4 | NA18963.hp1 NA19011.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+6775dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2698185 | |||||
| chrX:2698185
|
C | CTT | 7 | a0001c0001t0001g0069a0001c0001t0001g0096a0001c0001t0001g0097others(4): Show | 7 | HG00544.hp2 HG02080.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+6774_67+6775dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2698185 | |||||
| chrX:2698185
|
CT | C | 4 | a0001c0001t0001g0178a0001c0002t0001g0125a0001c0014t0001g0193others(1): Show | 4 | HG01975.hp1 HG03486.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+6775delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2698185 | |||||
| chrX:2698202
|
T | A | 2 | a0001c0001t0001g0004a0001c0001t0002g0098 | 2 | HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.67+6775T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698202 | ||||||
| chrX:2698217
|
C | T | 14 | a0001c0001t0001g0006a0001c0001t0001g0169a0001c0001t0001g0194others(11): Show | 14 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+6790C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698217 | ||||||
| chrX:2698380
|
G | C | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0172others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+6953G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698380 | ||||||
| chrX:2698416
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0106a0001c0001t0001g0155 | 3 | HG00544.hp2 HG02080.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.67+6989G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698416 | ||||||
| chrX:2698422
|
G | A | 2 | a0001c0001t0001g0174a0001c0004t0001g0171 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.67+6995G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698422 | ||||||
| chrX:2698475
|
C | A | 4 | a0001c0001t0001g0169a0001c0001t0001g0217a0001c0001t0006g0220others(1): Show | 4 | HG02109.hp2 HG02559.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+7048C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698475 | ||||||
| chrX:2698549
|
C | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0169a0001c0001t0001g0175others(17): Show | 20 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.67+7122C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698549 | ||||||
| chrX:2698739
|
C | T | 98 | a0001c0001t0001g0044a0001c0001t0001g0072a0001c0001t0001g0073others(95): Show | 100 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.67+7312C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698739 | ||||||
| chrX:2698744
|
C | T | 2 | a0001c0001t0001g0174a0001c0004t0001g0171 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.67+7317C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698744 | ||||||
| chrX:2698770
|
G | T | 1 | a0001c0014t0001g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.67+7343G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698770 | ||||||
| chrX:2698784
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.67+7357C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698784 | ||||||
| chrX:2698850
|
C | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0096a0001c0001t0001g0097others(17): Show | 20 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.67+7423C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698850 | ||||||
| chrX:2698851
|
A | G | 136 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(133): Show | 138 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.67+7424A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698851 | ||||||
| chrX:2698929
|
A | AT | 8 | a0001c0001t0001g0081a0001c0001t0001g0104a0001c0001t0001g0105others(5): Show | 8 | HG00423.hp1 NA18941.hp2 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+7517dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2698929 | |||||
| chrX:2698929
|
AT | A | 9 | a0001c0001t0001g0076a0001c0001t0001g0175a0001c0001t0001g0194others(6): Show | 9 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+7517delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2698929 | |||||
| chrX:2698936
|
T | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0092a0001c0001t0001g0108others(3): Show | 6 | HG02809.hp2 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+7509T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698936 | ||||||
| chrX:2698953
|
A | AT | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.67+7530dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2698953 | |||||
| chrX:2698953
|
A | G | 1 | a0001c0001t0001g0002 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.67+7526A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2698953 | ||||||
| chrX:2699110
|
G | GT | 21 | a0001c0001t0001g0006a0001c0001t0001g0096a0001c0001t0001g0097others(18): Show | 21 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.67+7690dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2699110 | |||||
| chrX:2699130
|
CTTCTTTT others(3): Show |
C | 17 | a0001c0001t0001g0006a0001c0001t0001g0169a0001c0001t0001g0175others(14): Show | 17 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.67+7711_67+7720del others(10): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2699130 | |||||
| chrX:2699155
|
CT | C | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+7730delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2699155 | |||||
| chrX:2699168
|
TTTC | T | 1 | a0001c0001t0001g0198 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+7753_67+7755del others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2699168 | |||||
| chrX:2699180
|
CT | C | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+7761delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2699180 | |||||
| chrX:2699259
|
TC | T | 1 | a0001c0001t0001g0178 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.67+7835delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2699259 | |||||
| chrX:2699349
|
T | TTC | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+7922_67+7923ins others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699349 | ||||||
| chrX:2699355
|
A | G | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+7928A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699355 | ||||||
| chrX:2699362
|
A | G | 223 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(220): Show | 227 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.67+7935A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699362 | ||||||
| chrX:2699377
|
C | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0170 | 2 | HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.67+7950C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699377 | ||||||
| chrX:2699437
|
G | C | 3 | a0001c0001t0002g0033a0001c0001t0005g0223a0001c0011t0001g0202 | 3 | HG02615.hp2 HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.67+8010G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699437 | ||||||
| chrX:2699467
|
C | CT | 37 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0032others(34): Show | 37 | HG00099.hp2 HG00735.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.67+8060dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2699467 | |||||
| chrX:2699467
|
C | CTT | 4 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0097others(1): Show | 4 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+8059_67+8060dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2699467 | |||||
| chrX:2699467
|
C | CTTT | 1 | a0002c0003t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.67+8058_67+8060dup others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2699467 | |||||
| chrX:2699467
|
CT | C | 2 | a0001c0001t0003g0152a0001c0001t0005g0223 | 2 | HG03195.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.67+8060delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2699467 | |||||
| chrX:2699470
|
T | C | 1 | a0001c0002t0010g0135 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.67+8043T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699470 | ||||||
| chrX:2699572
|
G | A | 1 | a0001c0002t0001g0029 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.67+8145G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699572 | ||||||
| chrX:2699583
|
G | T | 66 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(63): Show | 68 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.67+8156G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699583 | ||||||
| chrX:2699640
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.67+8213A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699640 | ||||||
| chrX:2699761
|
G | A | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67+8334G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699761 | ||||||
| chrX:2699769
|
TA | T | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+8347delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2699769 | |||||
| chrX:2699855
|
A | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0002g0098others(1): Show | 4 | HG02622.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+8428A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2699855 | ||||||
| chrX:2699881
|
CG | C | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+8456delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2699881 | |||||
| chrX:2700047
|
A | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(3): Show | 6 | HG02257.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+8620A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2700047 | ||||||
| chrX:2700108
|
TG | T | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+8684delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2700108 | |||||
| chrX:2700153
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.67+8726C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2700153 | ||||||
| chrX:2700202
|
T | A | 1 | a0001c0001t0001g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.67+8775T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2700202 | ||||||
| chrX:2700271
|
T | G | 1 | a0001c0002t0002g0167 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.67+8844T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2700271 | ||||||
| chrX:2700356
|
T | C | 1 | a0001c0002t0001g0109 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.67+8929T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2700356 | ||||||
| chrX:2700434
|
TC | T | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+9010delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2700434 | |||||
| chrX:2700462
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+9035G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2700462 | ||||||
| chrX:2700462
|
GTCCA | G | 1 | a0001c0001t0001g0216 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.67+9050_67+9053del others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2700462 | |||||
| chrX:2700463
|
TC | T | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+9038delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2700463 | |||||
| chrX:2700522
|
ATGCATCC others(13): Show |
A | 1 | a0002c0003t0001g0151 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.67+9113_67+9132del others(20): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2700522 | |||||
| chrX:2700556
|
C | G | 1 | a0001c0001t0001g0067 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.67+9129C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2700556 | ||||||
| chrX:2700561
|
T | TATCC | 2 | a0002c0003t0001g0221a0002c0003t0001g0222 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.67+9155_67+9158dup others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2700561 | |||||
| chrX:2700643
|
C | G | 9 | a0001c0001t0001g0006a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+9216C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2700643 | ||||||
| chrX:2700683
|
CT | C | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+9260delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2700683 | |||||
| chrX:2700784
|
A | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG00741.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.67+9357A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2700784 | ||||||
| chrX:2700797
|
T | C | 16 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0038others(13): Show | 16 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.67+9370T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2700797 | ||||||
| chrX:2701112
|
G | GA | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.67+9685_67+9686ins others(1): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701112 | ||||||
| chrX:2701207
|
G | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG00741.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.67+9780G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701207 | ||||||
| chrX:2701245
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.67+9818A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701245 | ||||||
| chrX:2701291
|
C | G | 1 | a0002c0003t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.67+9864C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701291 | ||||||
| chrX:2701298
|
A | G | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0172others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+9871A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701298 | ||||||
| chrX:2701381
|
T | C | 16 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0038others(13): Show | 16 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.67+9954T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701381 | ||||||
| chrX:2701430
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.67+10003G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701430 | ||||||
| chrX:2701436
|
T | C | 121 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 123 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.67+10009T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701436 | ||||||
| chrX:2701483
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.67+10056A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701483 | ||||||
| chrX:2701585
|
GCCT | G | 131 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(128): Show | 133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.67+10160_67+10162d others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2701585 | |||||
| chrX:2701589
|
C | T | 131 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(128): Show | 133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.67+10162C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701589 | ||||||
| chrX:2701590
|
T | G | 131 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(128): Show | 133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.67+10163T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701590 | ||||||
| chrX:2701613
|
T | G | 99 | a0001c0001t0001g0044a0001c0001t0001g0072a0001c0001t0001g0073others(96): Show | 101 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.67+10186T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701613 | ||||||
| chrX:2701721
|
C | T | 3 | a0003c0008t0004g0087a0003c0008t0004g0088a0003c0008t0004g0089 | 3 | HG02896.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.67+10294C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2701721 | ||||||
| chrX:2702007
|
A | T | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.67+10580A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702007 | ||||||
| chrX:2702051
|
TA | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+10626delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2702051 | |||||
| chrX:2702130
|
A | G | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0172others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+10703A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702130 | ||||||
| chrX:2702174
|
C | T | 3 | a0001c0001t0001g0204a0001c0002t0001g0123a0001c0014t0001g0193 | 3 | HG02809.hp2 HG03486.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.67+10747C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702174 | ||||||
| chrX:2702187
|
G | C | 3 | a0003c0008t0004g0087a0003c0008t0004g0088a0003c0008t0004g0089 | 3 | HG02896.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.67+10760G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702187 | ||||||
| chrX:2702284
|
A | G | 3 | a0003c0008t0004g0087a0003c0008t0004g0088a0003c0008t0004g0089 | 3 | HG02896.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.67+10857A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702284 | ||||||
| chrX:2702294
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.67+10867C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702294 | ||||||
| chrX:2702426
|
CAAT | C | 13 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0038others(10): Show | 13 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.67+11000_67+11002d others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702426 | ||||||
| chrX:2702449
|
G | A | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0172others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+11022G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702449 | ||||||
| chrX:2702469
|
T | G | 2 | a0001c0001t0002g0085a0001c0001t0002g0086 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.67+11042T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702469 | ||||||
| chrX:2702499
|
C | T | 1 | a0001c0002t0001g0150 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.67+11072C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702499 | ||||||
| chrX:2702595
|
C | G | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0172others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+11168C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702595 | ||||||
| chrX:2702620
|
T | C | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG02886.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+11193T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702620 | ||||||
| chrX:2702764
|
C | T | 1 | a0001c0002t0001g0123 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.67+11337C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702764 | ||||||
| chrX:2702779
|
A | T | 3 | a0001c0001t0001g0178a0001c0001t0001g0182a0001c0001t0002g0184 | 3 | NA18939.hp1 NA18998.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.67+11352A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702779 | ||||||
| chrX:2702780
|
C | CT | 3 | a0003c0008t0004g0087a0003c0008t0004g0088a0003c0008t0004g0089 | 3 | HG02896.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.67+11364dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2702780 | |||||
| chrX:2702781
|
T | C | 20 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0069others(17): Show | 20 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+11354T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702781 | ||||||
| chrX:2702816
|
C | T | 3 | a0001c0001t0001g0178a0001c0001t0001g0182a0001c0001t0002g0184 | 3 | NA18939.hp1 NA18998.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.67+11389C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702816 | ||||||
| chrX:2702818
|
T | G | 20 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0069others(17): Show | 20 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+11391T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702818 | ||||||
| chrX:2702977
|
C | T | 4 | a0001c0001t0001g0169a0001c0001t0001g0217a0001c0001t0006g0220others(1): Show | 4 | HG02109.hp2 HG02559.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-11445C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2702977 | ||||||
| chrX:2703035
|
C | T | 3 | a0001c0001t0001g0108a0001c0001t0002g0101a0001c0001t0002g0102 | 3 | HG01891.hp2 HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.68-11387C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703035 | ||||||
| chrX:2703063
|
A | G | 2 | a0002c0003t0001g0221a0002c0003t0001g0222 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.68-11359A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703063 | ||||||
| chrX:2703069
|
G | C | 6 | a0001c0001t0001g0108a0001c0001t0002g0101a0001c0001t0002g0102others(3): Show | 6 | HG01891.hp2 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-11353G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703069 | ||||||
| chrX:2703078
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0002g0098others(2): Show | 5 | HG02622.hp2 HG02723.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-11344C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703078 | ||||||
| chrX:2703079
|
A | G | 144 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(141): Show | 146 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.68-11343A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703079 | ||||||
| chrX:2703106
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.68-11316T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703106 | ||||||
| chrX:2703245
|
G | A | 1 | a0001c0002t0002g0167 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.68-11177G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703245 | ||||||
| chrX:2703287
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.68-11135G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703287 | ||||||
| chrX:2703371
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.68-11051G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703371 | ||||||
| chrX:2703417
|
G | A | 130 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0044others(127): Show | 132 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.68-11005G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703417 | ||||||
| chrX:2703444
|
A | G | 1 | a0001c0004t0001g0149 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.68-10978A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703444 | ||||||
| chrX:2703524
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0170 | 2 | HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.68-10898C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703524 | ||||||
| chrX:2703587
|
TAAC | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0069a0001c0001t0001g0081others(8): Show | 11 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(8): Show |
intron_variant | MODIFIER | c.68-10832_68-10830d others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703587 | |||||
| chrX:2703602
|
T | TTG | 4 | a0001c0001t0001g0194a0001c0001t0006g0196a0003c0009t0001g0190others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-10819_68-10818i others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703602 | |||||
| chrX:2703602
|
T | TTGTG | 1 | a0001c0001t0001g0195 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.68-10819_68-10818i others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703602 | |||||
| chrX:2703602
|
TTAAGTG | T | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.68-10818_68-10813d others(8): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703602 | |||||
| chrX:2703603
|
TAA | T | 3 | a0001c0001t0002g0085a0001c0001t0002g0086a0002c0003t0001g0005 | 3 | HG01070.hp1 HG01071.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.68-10818_68-10817d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703603 | ||||||
| chrX:2703604
|
A | G | 8 | a0001c0001t0001g0006a0001c0001t0001g0194a0001c0001t0001g0195others(5): Show | 8 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-10818A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703604 | ||||||
| chrX:2703605
|
A | AGT | 49 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0001t0001g0052others(46): Show | 50 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.68-10772_68-10771d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | |||||
| chrX:2703605
|
A | AGTGT | 14 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0065others(11): Show | 14 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-10774_68-10771d others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | |||||
| chrX:2703605
|
A | AGTGTGT | 4 | a0001c0001t0001g0095a0001c0002t0001g0110a0001c0006t0001g0140others(1): Show | 4 | HG02630.hp2 NA19077.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-10776_68-10771d others(8): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | |||||
| chrX:2703605
|
A | AGTGTGTG others(1): Show |
3 | a0001c0001t0001g0073a0001c0002t0001g0150a0001c0002t0001g0154 | 3 | HG02165.hp2 NA19084.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.68-10778_68-10771d others(10): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | |||||
| chrX:2703605
|
A | AGTGTGTG others(3): Show |
8 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0005g0093others(5): Show | 10 | HG01884.hp2 NA18965.hp1 NA18972.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-10780_68-10771d others(12): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | |||||
| chrX:2703605
|
A | AGTGTGTG others(5): Show |
4 | a0001c0001t0001g0075a0001c0001t0001g0133a0001c0001t0001g0136others(1): Show | 4 | HG02559.hp1 NA18985.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-10782_68-10771d others(14): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | |||||
| chrX:2703605
|
A | AGTGTGTG others(7): Show |
1 | a0001c0001t0001g0074 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.68-10784_68-10771d others(16): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | |||||
| chrX:2703605
|
A | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0194a0001c0001t0001g0195others(5): Show | 8 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-10817A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703605 | ||||||
| chrX:2703605
|
AGT | A | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0061others(15): Show | 18 | HG00558.hp1 HG00735.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.68-10772_68-10771d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | |||||
| chrX:2703605
|
AGTGT | A | 31 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(28): Show | 31 | HG00423.hp1 HG00438.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.68-10774_68-10771d others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | |||||
| chrX:2703605
|
AGTGTGT | A | 8 | a0001c0001t0001g0069a0001c0001t0001g0100a0001c0001t0001g0106others(5): Show | 8 | HG00544.hp2 HG01123.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-10776_68-10771d others(8): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | |||||
| chrX:2703605
|
AGTGTGTG others(1): Show |
A | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.68-10778_68-10771d others(10): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | |||||
| chrX:2703605
|
AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0002g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.68-10780_68-10771d others(12): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | |||||
| chrX:2703605
|
AGTGTGTG others(5): Show |
A | 2 | a0001c0001t0001g0108a0001c0001t0001g0215 | 2 | HG06807.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.68-10782_68-10771d others(14): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | |||||
| chrX:2703605
|
AGTGTGTG others(17): Show |
A | 4 | a0001c0001t0002g0102a0003c0008t0004g0087a0003c0008t0004g0088others(1): Show | 4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-10794_68-10771d others(26): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703605 | |||||
| chrX:2703663
|
C | A | 1 | a0001c0001t0002g0185 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.68-10759C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703663 | ||||||
| chrX:2703717
|
AG | A | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.68-10701delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2703717 | |||||
| chrX:2703829
|
C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0038a0002c0003t0001g0099others(1): Show | 4 | HG02622.hp2 HG03669.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-10593C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703829 | ||||||
| chrX:2703896
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0096others(5): Show | 8 | HG02622.hp2 HG02630.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-10526G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2703896 | ||||||
| chrX:2704041
|
T | C | 99 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0044others(96): Show | 101 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.68-10381T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704041 | ||||||
| chrX:2704165
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.68-10257A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704165 | ||||||
| chrX:2704194
|
TA | T | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.68-10224delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2704194 | |||||
| chrX:2704219
|
G | A | 128 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(125): Show | 130 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.68-10203G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704219 | ||||||
| chrX:2704377
|
C | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-10045C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704377 | ||||||
| chrX:2704389
|
A | AG | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.68-10032dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2704389 | |||||
| chrX:2704396
|
G | GCAGTTTA others(2): Show |
4 | a0001c0001t0001g0004a0001c0001t0001g0038a0002c0003t0001g0099others(1): Show | 4 | HG02622.hp2 HG03669.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-10023_68-10015d others(11): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2704396 | |||||
| chrX:2704415
|
A | C | 1 | a0001c0014t0001g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.68-10007A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704415 | ||||||
| chrX:2704532
|
CA | C | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.68-9888delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2704532 | |||||
| chrX:2704606
|
C | T | 140 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(137): Show | 142 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.68-9816C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704606 | ||||||
| chrX:2704624
|
T | G | 131 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(128): Show | 133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.68-9798T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704624 | ||||||
| chrX:2704750
|
G | C | 1 | a0001c0001t0005g0223 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.68-9672G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704750 | ||||||
| chrX:2704855
|
TG | T | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.68-9564delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2704855 | |||||
| chrX:2704904
|
G | A | 4 | a0001c0001t0001g0169a0001c0001t0001g0217a0001c0001t0005g0034others(1): Show | 4 | HG02109.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-9518G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704904 | ||||||
| chrX:2704936
|
A | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0038 | 2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.68-9486A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2704936 | ||||||
| chrX:2705002
|
A | G | 43 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0108others(40): Show | 43 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.68-9420A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705002 | ||||||
| chrX:2705026
|
AT | A | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.68-9392delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2705026 | |||||
| chrX:2705052
|
C | T | 1 | a0001c0005t0001g0210 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.68-9370C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705052 | ||||||
| chrX:2705069
|
A | G | 1 | a0001c0014t0001g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.68-9353A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705069 | ||||||
| chrX:2705112
|
G | A | 87 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0044others(84): Show | 89 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.68-9310G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705112 | ||||||
| chrX:2705152
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0170 | 2 | HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.68-9270C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705152 | ||||||
| chrX:2705183
|
T | TG | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.68-9237dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2705183 | |||||
| chrX:2705228
|
G | A | 1 | a0001c0001t0005g0223 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.68-9194G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705228 | ||||||
| chrX:2705314
|
G | A | 1 | a0002c0007t0001g0028 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.68-9108G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705314 | ||||||
| chrX:2705382
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.68-9040A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705382 | ||||||
| chrX:2705408
|
A | AT | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.68-9010dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2705408 | |||||
| chrX:2705504
|
C | T | 98 | a0001c0001t0001g0044a0001c0001t0001g0072a0001c0001t0001g0073others(95): Show | 100 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.68-8918C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705504 | ||||||
| chrX:2705669
|
C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0038a0002c0003t0001g0099others(1): Show | 4 | HG02622.hp2 HG03669.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-8753C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705669 | ||||||
| chrX:2705731
|
T | C | 1 | a0001c0011t0001g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.68-8691T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705731 | ||||||
| chrX:2705906
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0038a0002c0003t0001g0099others(1): Show | 4 | HG02622.hp2 HG03669.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-8516G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2705906 | ||||||
| chrX:2705986
|
G | GC | 1 | a0001c0001t0002g0156 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.68-8430dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2705986 | |||||
| chrX:2706040
|
C | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-8382C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706040 | ||||||
| chrX:2706063
|
G | GA | 7 | a0001c0001t0001g0030a0001c0001t0001g0044a0001c0001t0001g0092others(4): Show | 7 | HG02723.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-8346dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2706063 | |||||
| chrX:2706063
|
G | GAA | 125 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(122): Show | 128 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.68-8347_68-8346dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2706063 | |||||
| chrX:2706063
|
G | GAAA | 1 | a0001c0001t0003g0152 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.68-8348_68-8346dup others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2706063 | |||||
| chrX:2706063
|
GA | G | 3 | a0001c0001t0001g0081a0001c0002t0001g0115a0001c0011t0001g0202 | 3 | NA19003.hp2 NA19081.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.68-8346delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2706063 | |||||
| chrX:2706079
|
G | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0069a0001c0001t0001g0081others(8): Show | 11 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(8): Show |
intron_variant | MODIFIER | c.68-8343G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706079 | ||||||
| chrX:2706097
|
C | T | 1 | a0001c0001t0001g0007 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.68-8325C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706097 | ||||||
| chrX:2706145
|
T | G | 127 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(124): Show | 130 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.68-8277T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706145 | ||||||
| chrX:2706156
|
G | C | 1 | a0001c0002t0001g0042 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.68-8266G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706156 | ||||||
| chrX:2706183
|
C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0038a0002c0003t0001g0099others(1): Show | 4 | HG02622.hp2 HG03669.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-8239C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706183 | ||||||
| chrX:2706354
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(174): Show | 180 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.68-8068T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706354 | ||||||
| chrX:2706368
|
G | A | 140 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(137): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.68-8054G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706368 | ||||||
| chrX:2706426
|
A | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(162): Show | 168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.68-7996A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706426 | ||||||
| chrX:2706483
|
C | T | 35 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 36 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.68-7939C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706483 | ||||||
| chrX:2706653
|
TC | T | 1 | a0001c0005t0001g0129 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.68-7766delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2706653 | |||||
| chrX:2706666
|
G | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0194a0001c0001t0001g0195others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-7756G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706666 | ||||||
| chrX:2706731
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(4): Show | 7 | HG02257.hp2 HG02622.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.68-7691G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706731 | ||||||
| chrX:2706770
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.68-7652T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706770 | ||||||
| chrX:2706816
|
T | A | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.68-7606T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706816 | ||||||
| chrX:2706829
|
A | T | 2 | a0001c0001t0002g0085a0001c0001t0002g0086 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.68-7593A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706829 | ||||||
| chrX:2706888
|
T | G | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.68-7534T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706888 | ||||||
| chrX:2706889
|
C | T | 2 | a0001c0001t0001g0063a0004c0012t0007g0013 | 2 | HG01071.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.68-7533C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706889 | ||||||
| chrX:2706890
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.68-7532G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2706890 | ||||||
| chrX:2707055
|
C | T | 2 | a0001c0002t0001g0122a0002c0007t0001g0112 | 2 | NA18963.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.68-7367C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707055 | ||||||
| chrX:2707056
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(4): Show | 7 | HG02257.hp2 HG02622.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.68-7366G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707056 | ||||||
| chrX:2707097
|
AG | A | 1 | a0001c0005t0001g0129 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.68-7323delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707097 | |||||
| chrX:2707174
|
A | G | 4 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0002g0025others(1): Show | 4 | HG00733.hp2 HG00735.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-7248A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707174 | ||||||
| chrX:2707244
|
C | T | 6 | a0001c0002t0001g0134a0001c0002t0001g0147a0001c0002t0001g0150others(3): Show | 6 | NA18977.hp1 NA18981.hp1 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-7178C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707244 | ||||||
| chrX:2707329
|
C | CAAAAG | 65 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(62): Show | 65 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.68-7073_68-7069dup others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707329 | |||||
| chrX:2707329
|
C | CAAAAGAA others(3): Show |
35 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 35 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.68-7078_68-7069dup others(10): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707329 | |||||
| chrX:2707329
|
CAAAAG | C | 48 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0072others(45): Show | 50 | HG00408.hp1 HG01175.hp2 HG01346.hp2 others(47): Show |
intron_variant | MODIFIER | c.68-7073_68-7069del others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707329 | |||||
| chrX:2707329
|
CAAAAGAA others(3): Show |
C | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0172others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-7078_68-7069del others(10): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707329 | |||||
| chrX:2707339
|
G | GAA | 1 | a0001c0014t0001g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.68-7080_68-7079dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707339 | |||||
| chrX:2707349
|
G | GA | 1 | a0001c0005t0001g0129 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.68-7066dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707349 | |||||
| chrX:2707349
|
G | GAAAAGAA | 2 | a0001c0001t0001g0002a0001c0001t0009g0064 | 3 | HG01516.hp1 HG01517.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.68-7069_68-7068ins others(7): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707349 | |||||
| chrX:2707378
|
A | G | 1 | a0001c0011t0001g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.68-7044A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707378 | ||||||
| chrX:2707402
|
C | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(169): Show | 175 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.68-7020C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707402 | ||||||
| chrX:2707403
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.68-7019C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707403 | ||||||
| chrX:2707443
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.68-6979G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707443 | ||||||
| chrX:2707462
|
AC | A | 2 | a0001c0001t0001g0174a0001c0004t0001g0171 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.68-6956delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707462 | |||||
| chrX:2707502
|
G | GT | 6 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(3): Show | 6 | HG02257.hp2 HG02622.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-6914dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707502 | |||||
| chrX:2707581
|
GC | G | 1 | a0001c0001t0001g0136 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.68-6839delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707581 | |||||
| chrX:2707591
|
G | A | 1 | a0001c0001t0001g0067 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.68-6831G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707591 | ||||||
| chrX:2707657
|
CG | C | 1 | a0001c0001t0001g0080 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.68-6762delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707657 | |||||
| chrX:2707679
|
T | C | 6 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0102others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-6743T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707679 | ||||||
| chrX:2707725
|
G | A | 60 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0072others(57): Show | 62 | HG00408.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.68-6697G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707725 | ||||||
| chrX:2707881
|
G | A | 54 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0072others(51): Show | 56 | HG00408.hp1 HG01175.hp2 HG01346.hp2 others(53): Show |
intron_variant | MODIFIER | c.68-6541G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707881 | ||||||
| chrX:2707888
|
T | C | 1 | a0001c0014t0001g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.68-6534T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707888 | ||||||
| chrX:2707896
|
G | GC | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.68-6523dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707896 | |||||
| chrX:2707929
|
A | AG | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.68-6490dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2707929 | |||||
| chrX:2707984
|
G | C | 1 | a0002c0007t0001g0020 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.68-6438G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2707984 | ||||||
| chrX:2708102
|
TACACCTG others(20): Show |
T | 3 | a0001c0001t0001g0107a0001c0004t0001g0149a0001c0004t0002g0082 | 3 | HG01884.hp1 HG02451.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.68-6301_68-6275del others(27): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2708102 | |||||
| chrX:2708119
|
C | T | 2 | a0001c0001t0001g0175a0001c0011t0001g0202 | 2 | HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.68-6303C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708119 | ||||||
| chrX:2708121
|
T | C | 173 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(170): Show | 176 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.68-6301T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708121 | ||||||
| chrX:2708187
|
A | G | 23 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(20): Show | 23 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-6235A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708187 | ||||||
| chrX:2708301
|
A | G | 3 | a0001c0001t0001g0169a0001c0001t0001g0217a0001c0001t0006g0220 | 3 | HG02109.hp2 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-6121A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708301 | ||||||
| chrX:2708397
|
A | G | 1 | a0001c0011t0001g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.68-6025A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708397 | ||||||
| chrX:2708497
|
A | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0192 | 2 | HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.68-5925A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708497 | ||||||
| chrX:2708584
|
TA | T | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.68-5833delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2708584 | |||||
| chrX:2708661
|
A | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(173): Show | 179 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.68-5761A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708661 | ||||||
| chrX:2708676
|
A | AG | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.68-5745dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2708676 | |||||
| chrX:2708772
|
T | TG | 1 | a0001c0001t0001g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.68-5646dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2708772 | |||||
| chrX:2708812
|
C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0038a0002c0003t0001g0099others(1): Show | 4 | HG02622.hp2 HG03669.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-5610C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708812 | ||||||
| chrX:2708819
|
C | T | 3 | a0001c0001t0001g0107a0001c0004t0001g0149a0001c0004t0002g0082 | 3 | HG01884.hp1 HG02451.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.68-5603C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708819 | ||||||
| chrX:2708881
|
G | A | 1 | a0001c0001t0002g0183 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.68-5541G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708881 | ||||||
| chrX:2708933
|
C | A | 48 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0072others(45): Show | 50 | HG00408.hp1 HG01175.hp2 HG01346.hp2 others(47): Show |
intron_variant | MODIFIER | c.68-5489C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708933 | ||||||
| chrX:2708934
|
A | G | 48 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0072others(45): Show | 50 | HG00408.hp1 HG01175.hp2 HG01346.hp2 others(47): Show |
intron_variant | MODIFIER | c.68-5488A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2708934 | ||||||
| chrX:2709126
|
G | A | 5 | a0001c0002t0001g0042a0001c0002t0001g0043a0001c0002t0001g0045others(2): Show | 5 | HG02683.hp2 HG03704.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-5296G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709126 | ||||||
| chrX:2709161
|
CCAGA | C | 2 | a0001c0001t0002g0085a0001c0001t0002g0086 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.68-5254_68-5251del others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2709161 | |||||
| chrX:2709203
|
A | ACATGCAT others(24): Show |
31 | a0001c0002t0001g0008a0001c0002t0001g0016a0001c0002t0001g0017others(28): Show | 31 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.68-5205_68-5175dup others(31): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2709203 | |||||
| chrX:2709280
|
G | A | 23 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(20): Show | 23 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-5142G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709280 | ||||||
| chrX:2709310
|
GCA | G | 42 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(39): Show | 43 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.68-5109_68-5108del others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2709310 | |||||
| chrX:2709500
|
TCA | T | 1 | a0001c0001t0001g0198 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.68-4919_68-4918del others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2709500 | |||||
| chrX:2709546
|
C | CAT | 4 | a0001c0001t0001g0092a0001c0001t0001g0192a0001c0001t0001g0204others(1): Show | 4 | HG02723.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-4871_68-4870dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2709546 | |||||
| chrX:2709578
|
A | G | 1 | a0001c0002t0001g0121 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.68-4844A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709578 | ||||||
| chrX:2709600
|
GCA | G | 6 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0172others(3): Show | 6 | HG02630.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-4816_68-4815del others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2709600 | |||||
| chrX:2709608
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.68-4814G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709608 | ||||||
| chrX:2709619
|
G | C | 23 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(20): Show | 23 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-4803G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709619 | ||||||
| chrX:2709642
|
C | T | 1 | a0001c0014t0001g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.68-4780C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709642 | ||||||
| chrX:2709650
|
T | G | 1 | a0001c0002t0002g0167 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.68-4772T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709650 | ||||||
| chrX:2709663
|
T | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(105): Show | 109 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.68-4759T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709663 | ||||||
| chrX:2709669
|
T | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0136 | 2 | NA18989.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.68-4753T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709669 | ||||||
| chrX:2709697
|
A | AACATAGA others(15): Show |
41 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(38): Show | 42 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.68-4714_68-4693dup others(22): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2709697 | |||||
| chrX:2709708
|
A | ACACATGC others(15): Show |
1 | a0001c0001t0002g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.68-4693_68-4672dup others(22): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2709708 | |||||
| chrX:2709708
|
A | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0194a0001c0001t0001g0195others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-4714A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709708 | ||||||
| chrX:2709708
|
ACACATGC others(15): Show |
A | 1 | a0001c0002t0001g0128 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.68-4693_68-4672del others(22): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2709708 | |||||
| chrX:2709730
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0217a0001c0001t0006g0220 | 3 | HG02109.hp2 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-4692G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709730 | ||||||
| chrX:2709746
|
A | G | 1 | a0001c0011t0001g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.68-4676A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709746 | ||||||
| chrX:2709788
|
C | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(49): Show | 53 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.68-4634C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709788 | ||||||
| chrX:2709865
|
A | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0217a0001c0001t0006g0220 | 3 | HG02109.hp2 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-4557A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709865 | ||||||
| chrX:2709902
|
G | C | 1 | a0001c0001t0001g0007 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.68-4520G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709902 | ||||||
| chrX:2709944
|
A | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0092a0001c0001t0001g0192others(4): Show | 7 | HG02723.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-4478A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2709944 | ||||||
| chrX:2710018
|
C | T | 2 | a0001c0001t0001g0175a0001c0014t0001g0193 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.68-4404C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710018 | ||||||
| chrX:2710050
|
G | A | 1 | a0002c0003t0001g0099 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.68-4372G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710050 | ||||||
| chrX:2710088
|
A | G | 1 | a0001c0001t0009g0064 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.68-4334A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710088 | ||||||
| chrX:2710110
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.68-4312C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710110 | ||||||
| chrX:2710160
|
A | G | 55 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(52): Show | 56 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.68-4262A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710160 | ||||||
| chrX:2710165
|
G | A | 2 | a0003c0009t0001g0190a0003c0009t0001g0191 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.68-4257G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710165 | ||||||
| chrX:2710175
|
T | TC | 175 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(172): Show | 178 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.68-4246dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2710175 | |||||
| chrX:2710265
|
C | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0217a0001c0001t0006g0220 | 3 | HG02109.hp2 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-4157C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710265 | ||||||
| chrX:2710281
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0009g0064 | 4 | HG01516.hp1 HG01517.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-4141A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710281 | ||||||
| chrX:2710305
|
T | C | 2 | a0001c0001t0002g0085a0001c0001t0002g0086 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.68-4117T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710305 | ||||||
| chrX:2710375
|
A | C | 87 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 89 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.68-4047A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710375 | ||||||
| chrX:2710415
|
G | A | 1 | a0002c0003t0001g0151 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.68-4007G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710415 | ||||||
| chrX:2710438
|
G | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(35): Show | 38 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-3984G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710438 | ||||||
| chrX:2710442
|
A | G | 3 | a0001c0001t0001g0107a0001c0004t0001g0149a0001c0004t0002g0082 | 3 | HG01884.hp1 HG02451.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.68-3980A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710442 | ||||||
| chrX:2710492
|
GTACTT | G | 48 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0072others(45): Show | 50 | HG00408.hp1 HG01175.hp2 HG01346.hp2 others(47): Show |
intron_variant | MODIFIER | c.68-3923_68-3919del others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2710492 | |||||
| chrX:2710503
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.68-3919T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710503 | ||||||
| chrX:2710514
|
G | GT | 1 | a0001c0006t0001g0055 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.68-3899dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2710514 | |||||
| chrX:2710514
|
G | GTT | 2 | a0001c0001t0002g0085a0001c0001t0002g0086 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.68-3900_68-3899dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2710514 | |||||
| chrX:2710514
|
G | GTTT | 11 | a0001c0001t0001g0107a0001c0001t0001g0169a0001c0001t0001g0175others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.68-3901_68-3899dup others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2710514 | |||||
| chrX:2710514
|
G | GTTTT | 42 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(39): Show | 43 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.68-3902_68-3899dup others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2710514 | |||||
| chrX:2710514
|
G | GTTTTT | 1 | a0001c0001t0001g0054 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.68-3903_68-3899dup others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2710514 | |||||
| chrX:2710735
|
C | T | 3 | a0001c0001t0001g0107a0001c0004t0001g0149a0001c0004t0002g0082 | 3 | HG01884.hp1 HG02451.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.68-3687C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710735 | ||||||
| chrX:2710768
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0006g0196others(2): Show | 5 | HG01891.hp1 HG02622.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-3654A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710768 | ||||||
| chrX:2710774
|
G | A | 1 | a0001c0001t0001g0007 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.68-3648G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710774 | ||||||
| chrX:2710867
|
C | CT | 136 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(133): Show | 139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.68-3534dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2710867 | |||||
| chrX:2710867
|
C | CTT | 15 | a0001c0001t0001g0050a0001c0001t0001g0054a0001c0001t0001g0158others(12): Show | 15 | HG00408.hp2 HG00741.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.68-3535_68-3534dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2710867 | |||||
| chrX:2710867
|
C | CTTT | 2 | a0001c0004t0001g0149a0001c0004t0002g0082 | 2 | HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.68-3536_68-3534dup others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2710867 | |||||
| chrX:2710867
|
C | CTTTT | 1 | a0001c0001t0001g0107 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.68-3537_68-3534dup others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2710867 | |||||
| chrX:2710867
|
CT | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0194 | 2 | HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.68-3534delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2710867 | |||||
| chrX:2710907
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0217a0001c0001t0006g0220 | 3 | HG02109.hp2 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-3515G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710907 | ||||||
| chrX:2710950
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(100): Show | 106 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.68-3472A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2710950 | ||||||
| chrX:2711037
|
A | G | 56 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(53): Show | 57 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.68-3385A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711037 | ||||||
| chrX:2711042
|
T | C | 5 | a0001c0001t0001g0169a0001c0001t0001g0217a0001c0001t0002g0085others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-3380T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711042 | ||||||
| chrX:2711061
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(8): Show | 11 | HG01168.hp2 HG01169.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.68-3361C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711061 | ||||||
| chrX:2711134
|
G | A | 2 | a0001c0002t0001g0019a0001c0006t0001g0201 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.68-3288G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711134 | ||||||
| chrX:2711146
|
C | G | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.68-3276C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711146 | ||||||
| chrX:2711249
|
A | C | 3 | a0001c0001t0001g0053a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG02165.hp1 NA18981.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.68-3173A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711249 | ||||||
| chrX:2711259
|
T | G | 2 | a0001c0001t0002g0085a0001c0001t0002g0086 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.68-3163T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711259 | ||||||
| chrX:2711290
|
TGTATATA others(2): Show |
T | 1 | a0001c0002t0001g0041 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.68-3118_68-3110del others(9): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2711290 | |||||
| chrX:2711410
|
TA | T | 3 | a0001c0001t0001g0002a0001c0001t0002g0085a0001c0001t0002g0086 | 4 | HG01070.hp1 HG01071.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-3011delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711410 | ||||||
| chrX:2711411
|
AT | A | 47 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(44): Show | 47 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.68-3009delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2711411 | |||||
| chrX:2711412
|
T | G | 3 | a0001c0001t0001g0002a0001c0001t0002g0085a0001c0001t0002g0086 | 4 | HG01070.hp1 HG01071.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-3010T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711412 | ||||||
| chrX:2711412
|
T | TA | 4 | a0001c0001t0001g0049a0001c0001t0001g0217a0001c0001t0002g0033others(1): Show | 4 | HG02109.hp2 HG02155.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-3010_68-3009ins others(1): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711412 | ||||||
| chrX:2711412
|
T | TATA | 2 | a0001c0004t0001g0149a0001c0004t0002g0082 | 2 | HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.68-3010_68-3009ins others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711412 | ||||||
| chrX:2711412
|
TTA | T | 1 | a0001c0002t0001g0016 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.68-2997_68-2996del others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2711412 | |||||
| chrX:2711414
|
A | T | 1 | a0001c0001t0001g0044 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.68-3008A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711414 | ||||||
| chrX:2711435
|
ATGTG | A | 48 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0072others(45): Show | 50 | HG00408.hp1 HG01175.hp2 HG01346.hp2 others(47): Show |
intron_variant | MODIFIER | c.68-2983_68-2980del others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2711435 | |||||
| chrX:2711441
|
G | GTA | 13 | a0001c0001t0001g0069a0001c0001t0001g0081a0001c0001t0001g0104others(10): Show | 13 | HG00423.hp1 HG00544.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.68-2969_68-2968dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2711441 | |||||
| chrX:2711470
|
G | A | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0186 | 3 | HG02155.hp1 NA18979.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.68-2952G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711470 | ||||||
| chrX:2711471
|
G | A | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0186 | 3 | HG02155.hp1 NA18979.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.68-2951G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711471 | ||||||
| chrX:2711753
|
AGGTTGGC others(10): Show |
A | 1 | a0001c0001t0005g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.68-2666_68-2650del others(17): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2711753 | |||||
| chrX:2711766
|
G | A | 2 | a0001c0001t0001g0217a0001c0001t0006g0220 | 2 | HG02109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-2656G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711766 | ||||||
| chrX:2711767
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.68-2655C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711767 | ||||||
| chrX:2711836
|
T | A | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.68-2586T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711836 | ||||||
| chrX:2711837
|
C | G | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.68-2585C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711837 | ||||||
| chrX:2711915
|
G | A | 1 | a0003c0008t0004g0089 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.68-2507G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711915 | ||||||
| chrX:2711999
|
C | T | 3 | a0001c0005t0001g0129a0001c0005t0001g0130a0001c0005t0001g0131 | 3 | NA19006.hp1 NA19064.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.68-2423C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2711999 | ||||||
| chrX:2712013
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.68-2409G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712013 | ||||||
| chrX:2712068
|
G | T | 3 | a0001c0001t0001g0107a0001c0004t0001g0149a0001c0004t0002g0082 | 3 | HG01884.hp1 HG02451.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.68-2354G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712068 | ||||||
| chrX:2712107
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.68-2315G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712107 | ||||||
| chrX:2712203
|
C | T | 1 | a0001c0001t0001g0007 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.68-2219C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712203 | ||||||
| chrX:2712340
|
G | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(38): Show | 42 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.68-2082G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712340 | ||||||
| chrX:2712406
|
G | A | 23 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(20): Show | 23 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-2016G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712406 | ||||||
| chrX:2712422
|
GA | G | 61 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(58): Show | 61 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.68-1992delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2712422 | |||||
| chrX:2712430
|
AT | A | 2 | a0001c0001t0001g0177a0001c0001t0011g0176 | 2 | HG02080.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.68-1991delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712430 | ||||||
| chrX:2712480
|
G | A | 62 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(59): Show | 62 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.68-1942G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712480 | ||||||
| chrX:2712510
|
C | G | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.68-1912C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712510 | ||||||
| chrX:2712579
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(190): Show | 196 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.68-1843A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712579 | ||||||
| chrX:2712660
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.68-1762G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712660 | ||||||
| chrX:2712766
|
C | A | 1 | a0001c0001t0002g0102 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.68-1656C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712766 | ||||||
| chrX:2712776
|
TACAC | T | 2 | a0002c0003t0001g0221a0002c0003t0001g0222 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.68-1636_68-1633del others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2712776 | |||||
| chrX:2712804
|
C | T | 4 | a0001c0001t0001g0108a0001c0001t0002g0085a0001c0001t0002g0086others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-1618C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712804 | ||||||
| chrX:2712804
|
CGTG | C | 1 | a0001c0001t0005g0223 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.68-1616_68-1614del others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2712804 | |||||
| chrX:2712819
|
C | G | 1 | a0001c0001t0002g0102 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.68-1603C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712819 | ||||||
| chrX:2712858
|
C | G | 1 | a0001c0001t0002g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.68-1564C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712858 | ||||||
| chrX:2712975
|
TACAC | T | 23 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(20): Show | 23 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-1441_68-1438del others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2712975 | |||||
| chrX:2712994
|
A | G | 117 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(114): Show | 120 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.68-1428A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2712994 | ||||||
| chrX:2713009
|
C | T | 10 | a0001c0001t0001g0069a0001c0001t0001g0081a0001c0001t0001g0104others(7): Show | 10 | HG00423.hp1 HG00544.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-1413C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713009 | ||||||
| chrX:2713032
|
A | G | 2 | a0001c0001t0001g0069a0001c0001t0001g0106 | 2 | HG02080.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.68-1390A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713032 | ||||||
| chrX:2713063
|
CAT | C | 3 | a0001c0001t0001g0169a0001c0001t0001g0217a0001c0001t0006g0220 | 3 | HG02109.hp2 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-1357_68-1356del others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2713063 | |||||
| chrX:2713077
|
C | T | 23 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(20): Show | 23 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-1345C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713077 | ||||||
| chrX:2713085
|
C | G | 21 | a0001c0001t0001g0014a0001c0001t0001g0083a0001c0001t0001g0084others(18): Show | 21 | HG00741.hp1 HG01884.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.68-1337C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713085 | ||||||
| chrX:2713104
|
CAT | C | 2 | a0002c0003t0001g0099a0003c0008t0004g0071 | 2 | HG03669.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.68-1314_68-1313del others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2713104 | |||||
| chrX:2713131
|
TACAC | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(116): Show | 122 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.68-1285_68-1282del others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2713131 | |||||
| chrX:2713221
|
C | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0217a0001c0001t0006g0220 | 3 | HG02109.hp2 HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-1201C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713221 | ||||||
| chrX:2713232
|
A | G | 10 | a0001c0001t0001g0069a0001c0001t0001g0081a0001c0001t0001g0104others(7): Show | 10 | HG00423.hp1 HG00544.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-1190A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713232 | ||||||
| chrX:2713315
|
AAC | A | 61 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0038others(58): Show | 61 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.68-1102_68-1101del others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2713315 | |||||
| chrX:2713339
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.68-1083A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713339 | ||||||
| chrX:2713400
|
CACAT | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(115): Show | 121 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.68-1017_68-1014del others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2713400 | |||||
| chrX:2713459
|
T | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(116): Show | 122 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.68-963T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713459 | ||||||
| chrX:2713682
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68-740G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713682 | ||||||
| chrX:2713844
|
A | G | 1 | a0001c0002t0001g0021 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.68-578A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2713844 | ||||||
| chrX:2714148
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(91): Show | 97 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.68-274A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2714148 | ||||||
| chrX:2714231
|
A | T | 101 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(98): Show | 102 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.68-191A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | chrX | 2714231 | ||||||
| chrX:2714237
|
TCTTA | T | 1 | a0001c0002t0001g0166 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.68-181_68-178delAC others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2714237 | |||||
| chrX:2714293
|
T | TGTAAATT others(2452): Show |
1 | a0001c0001t0006g0220 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.68-117_68-116insTT others(2457): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2714293 | |||||
| chrX:2714293
|
T | TGTAAATT others(2452): Show |
1 | a0001c0001t0001g0217 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.68-117_68-116insTT others(2457): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 2714293 | |||||
| chrX:2714470
|
AT | A | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.100+22delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2714470 | |||||
| chrX:2714483
|
C | T | 1 | a0001c0004t0002g0082 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.100+29C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2714483 | ||||||
| chrX:2714560
|
A | G | 1 | a0001c0004t0001g0146 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.100+106A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2714560 | ||||||
| chrX:2714781
|
G | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(94): Show | 98 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.100+327G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2714781 | ||||||
| chrX:2715035
|
T | G | 1 | a0001c0001t0001g0174 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.100+581T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715035 | ||||||
| chrX:2715066
|
A | G | 63 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0038others(60): Show | 63 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.100+612A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715066 | ||||||
| chrX:2715091
|
G | A | 2 | a0001c0001t0001g0170a0001c0011t0001g0202 | 2 | HG02257.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.100+637G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715091 | ||||||
| chrX:2715094
|
G | C | 59 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0030others(56): Show | 59 | HG00741.hp1 HG01175.hp2 HG01346.hp2 others(56): Show |
intron_variant | MODIFIER | c.100+640G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715094 | ||||||
| chrX:2715198
|
C | A | 1 | a0001c0001t0001g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.100+744C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715198 | ||||||
| chrX:2715210
|
C | CT | 55 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0078others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.100+757dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2715210 | |||||
| chrX:2715212
|
A | G | 22 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0066others(19): Show | 23 | HG00544.hp1 HG00558.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.100+758A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715212 | ||||||
| chrX:2715227
|
TTGTCATC others(23): Show |
T | 1 | a0001c0001t0001g0217 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.100+776_100+805del others(30): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2715227 | |||||
| chrX:2715253
|
G | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(61): Show | 65 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.100+799G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715253 | ||||||
| chrX:2715412
|
G | A | 1 | a0001c0004t0002g0082 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.100+958G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715412 | ||||||
| chrX:2715433
|
A | G | 83 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(80): Show | 84 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.100+979A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715433 | ||||||
| chrX:2715566
|
A | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(113): Show | 118 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.100+1112A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715566 | ||||||
| chrX:2715583
|
C | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(113): Show | 118 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.100+1129C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715583 | ||||||
| chrX:2715601
|
G | A | 13 | a0001c0001t0001g0007a0001c0001t0001g0076a0001c0001t0001g0077others(10): Show | 13 | HG00741.hp1 HG02109.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.100+1147G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715601 | ||||||
| chrX:2715628
|
AC | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0194others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+1176delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2715628 | |||||
| chrX:2715648
|
A | C | 22 | a0001c0001t0001g0014a0001c0001t0001g0072a0001c0001t0001g0073others(19): Show | 22 | HG01884.hp1 HG01884.hp2 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.100+1194A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715648 | ||||||
| chrX:2715670
|
G | A | 22 | a0001c0001t0001g0014a0001c0001t0001g0072a0001c0001t0001g0073others(19): Show | 22 | HG01884.hp1 HG01884.hp2 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.100+1216G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715670 | ||||||
| chrX:2715731
|
C | A | 12 | a0001c0001t0001g0044a0001c0001t0001g0148a0001c0001t0001g0157others(9): Show | 12 | HG01175.hp2 HG01346.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.100+1277C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715731 | ||||||
| chrX:2715760
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(106): Show | 111 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.100+1306T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715760 | ||||||
| chrX:2715763
|
C | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(106): Show | 111 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.100+1309C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715763 | ||||||
| chrX:2715763
|
C | T | 5 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0217others(2): Show | 5 | HG00741.hp1 HG02109.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+1309C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715763 | ||||||
| chrX:2715792
|
G | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(107): Show | 112 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.100+1338G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715792 | ||||||
| chrX:2715939
|
A | G | 69 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0001g0060others(66): Show | 70 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.100+1485A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2715939 | ||||||
| chrX:2716016
|
A | AT | 5 | a0001c0001t0001g0186a0001c0002t0001g0128a0001c0004t0001g0171others(2): Show | 5 | HG01981.hp2 HG02293.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-1571dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2716016 | |||||
| chrX:2716016
|
AT | A | 11 | a0001c0001t0001g0061a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.101-1571delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2716016 | |||||
| chrX:2716016
|
ATT | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0108a0003c0008t0004g0089 | 3 | HG03486.hp1 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.101-1572_101-1571d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2716016 | |||||
| chrX:2716254
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.101-1351T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716254 | ||||||
| chrX:2716297
|
A | G | 1 | a0001c0001t0002g0156 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.101-1308A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716297 | ||||||
| chrX:2716310
|
C | T | 1 | a0001c0002t0001g0116 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.101-1295C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716310 | ||||||
| chrX:2716342
|
C | CA | 52 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0046others(49): Show | 52 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.101-1263_101-1262i others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716342 | ||||||
| chrX:2716342
|
C | CT | 2 | a0001c0001t0001g0159a0001c0004t0001g0149 | 2 | HG02818.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.101-1253dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2716342 | |||||
| chrX:2716342
|
CT | C | 2 | a0001c0001t0001g0133a0001c0002t0001g0042 | 2 | NA18989.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.101-1253delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2716342 | |||||
| chrX:2716352
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | NA19002.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.101-1253T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716352 | ||||||
| chrX:2716367
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0194others(2): Show | 5 | HG02451.hp1 HG02922.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-1238C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716367 | ||||||
| chrX:2716368
|
G | A | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0003c0008t0004g0087others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-1237G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716368 | ||||||
| chrX:2716393
|
G | C | 1 | a0001c0014t0001g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.101-1212G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716393 | ||||||
| chrX:2716463
|
A | C | 1 | a0001c0001t0001g0069 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.101-1142A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716463 | ||||||
| chrX:2716596
|
A | G | 1 | a0001c0002t0001g0016 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.101-1009A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716596 | ||||||
| chrX:2716722
|
C | T | 9 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.101-883C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716722 | ||||||
| chrX:2716780
|
A | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0046others(58): Show | 62 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.101-825A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716780 | ||||||
| chrX:2716879
|
G | A | 1 | a0001c0002t0001g0042 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.101-726G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2716879 | ||||||
| chrX:2717044
|
C | G | 2 | a0002c0003t0001g0221a0002c0003t0001g0222 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.101-561C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717044 | ||||||
| chrX:2717048
|
G | A | 10 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-557G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717048 | ||||||
| chrX:2717084
|
A | C | 125 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0011others(122): Show | 126 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.101-521A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717084 | ||||||
| chrX:2717087
|
C | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0038others(5): Show | 8 | HG02451.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.101-518C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717087 | ||||||
| chrX:2717203
|
C | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0046others(50): Show | 54 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.101-402C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717203 | ||||||
| chrX:2717222
|
C | T | 1 | a0001c0002t0001g0127 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.101-383C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717222 | ||||||
| chrX:2717241
|
G | A | 1 | a0001c0002t0001g0118 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.101-364G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717241 | ||||||
| chrX:2717347
|
C | CA | 34 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0031others(31): Show | 34 | HG00099.hp2 HG00735.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.101-242dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2717347 | |||||
| chrX:2717347
|
C | CAA | 43 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0051others(40): Show | 43 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.101-243_101-242dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2717347 | |||||
| chrX:2717347
|
C | CAAA | 17 | a0001c0001t0001g0053a0001c0001t0001g0104a0001c0001t0001g0106others(14): Show | 20 | HG01981.hp2 HG02080.hp2 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.101-244_101-242dup others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2717347 | |||||
| chrX:2717347
|
CA | C | 4 | a0001c0001t0001g0090a0001c0001t0002g0156a0001c0001t0011g0176others(1): Show | 4 | HG00639.hp1 HG03669.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-242delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2717347 | |||||
| chrX:2717347
|
CAA | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.101-243_101-242del others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2717347 | |||||
| chrX:2717379
|
C | T | 1 | a0004c0015t0007g0018 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.101-226C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717379 | ||||||
| chrX:2717447
|
T | C | 18 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0104others(15): Show | 21 | HG01981.hp2 HG02080.hp2 HG02165.hp1 others(18): Show |
intron_variant | MODIFIER | c.101-158T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717447 | ||||||
| chrX:2717448
|
G | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0011others(140): Show | 147 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.101-157G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717448 | ||||||
| chrX:2717479
|
G | GA | 1 | a0001c0002t0001g0137 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.101-120dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 2717479 | |||||
| chrX:2717579
|
C | G | 1 | a0001c0001t0001g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.101-26C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 2/9 | chrX | 2717579 | ||||||
| chrX:2717836
|
AG | A | 1 | a0001c0002t0001g0124 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.148+185delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2717836 | ||||||
| chrX:2717905
|
G | A | 5 | a0001c0001t0001g0189a0001c0001t0002g0085a0001c0001t0002g0086others(2): Show | 5 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+253G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2717905 | ||||||
| chrX:2717934
|
TC | T | 1 | a0001c0006t0001g0055 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.148+285delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2717934 | |||||
| chrX:2717937
|
C | CT | 9 | a0001c0001t0001g0108a0001c0001t0001g0169a0001c0001t0002g0184others(6): Show | 9 | HG00408.hp1 HG01981.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.148+306dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2717937 | |||||
| chrX:2717937
|
CT | C | 21 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(18): Show | 21 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.148+306delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2717937 | |||||
| chrX:2717937
|
CTT | C | 4 | a0001c0001t0002g0214a0001c0002t0001g0128a0001c0011t0001g0202others(1): Show | 4 | HG02293.hp2 HG02896.hp2 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.148+305_148+306del others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2717937 | |||||
| chrX:2717937
|
CTTT | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0030others(106): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.148+304_148+306del others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2717937 | |||||
| chrX:2717937
|
CTTTT | C | 1 | a0003c0009t0001g0190 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.148+303_148+306del others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2717937 | |||||
| chrX:2717996
|
C | A | 2 | a0001c0001t0001g0108a0003c0008t0004g0089 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.148+344C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2717996 | ||||||
| chrX:2718034
|
C | T | 114 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0030others(111): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.148+382C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718034 | ||||||
| chrX:2718041
|
A | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0030others(111): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.148+389A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718041 | ||||||
| chrX:2718146
|
G | A | 1 | a0001c0004t0001g0142 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.148+494G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718146 | ||||||
| chrX:2718210
|
G | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0011others(123): Show | 127 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.148+558G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718210 | ||||||
| chrX:2718226
|
CG | C | 2 | a0001c0002t0001g0029a0001c0002t0001g0137 | 2 | HG03834.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.148+576delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2718226 | |||||
| chrX:2718311
|
ATC | A | 1 | a0001c0002t0001g0137 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.148+664_148+665del others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2718311 | |||||
| chrX:2718340
|
T | C | 1 | a0001c0002t0001g0036 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.148+688T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718340 | ||||||
| chrX:2718351
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.148+699G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718351 | ||||||
| chrX:2718369
|
C | CT | 5 | a0001c0001t0001g0011a0001c0002t0001g0021a0001c0002t0001g0128others(2): Show | 5 | HG00733.hp1 HG01346.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+734dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2718369 | |||||
| chrX:2718369
|
CT | C | 3 | a0001c0001t0001g0158a0001c0002t0001g0037a0001c0002t0001g0123 | 3 | HG01993.hp1 HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.148+734delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2718369 | |||||
| chrX:2718372
|
T | TC | 1 | a0001c0002t0001g0137 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.148+720_148+721ins others(1): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718372 | ||||||
| chrX:2718373
|
T | C | 17 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0104others(14): Show | 20 | HG01981.hp2 HG02080.hp2 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.148+721T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718373 | ||||||
| chrX:2718494
|
A | G | 119 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0030others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.148+842A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718494 | ||||||
| chrX:2718499
|
G | C | 1 | a0001c0001t0001g0026 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.148+847G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718499 | ||||||
| chrX:2718615
|
C | T | 26 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0038others(23): Show | 29 | HG01981.hp2 HG02080.hp2 HG02165.hp1 others(26): Show |
intron_variant | MODIFIER | c.148+963C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718615 | ||||||
| chrX:2718661
|
AC | A | 1 | a0001c0002t0001g0137 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.149-997delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2718661 | |||||
| chrX:2718681
|
C | G | 1 | a0001c0002t0001g0008 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.149-980C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718681 | ||||||
| chrX:2718739
|
C | G | 2 | a0001c0001t0001g0108a0003c0008t0004g0089 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.149-922C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718739 | ||||||
| chrX:2718829
|
G | GT | 1 | a0001c0002t0001g0137 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.149-828dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2718829 | |||||
| chrX:2718973
|
G | A | 6 | a0001c0001t0001g0078a0001c0001t0001g0108a0001c0001t0002g0098others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.149-688G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2718973 | ||||||
| chrX:2719020
|
TC | T | 1 | a0001c0002t0001g0137 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.149-638delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2719020 | |||||
| chrX:2719048
|
A | G | 1 | a0001c0001t0002g0184 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.149-613A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2719048 | ||||||
| chrX:2719189
|
T | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.149-472T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2719189 | ||||||
| chrX:2719258
|
CA | C | 1 | a0001c0002t0001g0137 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.149-400delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2719258 | |||||
| chrX:2719259
|
A | G | 2 | a0001c0001t0001g0108a0003c0008t0004g0089 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.149-402A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2719259 | ||||||
| chrX:2719398
|
T | TC | 120 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0030others(117): Show | 121 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.149-259dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 2719398 | |||||
| chrX:2719466
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.149-195C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 3/9 | chrX | 2719466 | ||||||
| chrX:2719780
|
T | A | 5 | a0001c0001t0001g0078a0001c0001t0002g0098a0001c0001t0002g0102others(2): Show | 5 | HG01891.hp1 HG01891.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+75T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 4/9 | chrX | 2719780 | ||||||
| chrX:2719869
|
G | GTT | 1 | a0001c0002t0001g0137 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.193+168_193+169dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chrX | 2719869 | |||||
| chrX:2719960
|
G | T | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.193+255G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 4/9 | chrX | 2719960 | ||||||
| chrX:2720011
|
G | GT | 1 | a0001c0002t0001g0137 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.193+308dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chrX | 2720011 | |||||
| chrX:2720071
|
T | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0030others(115): Show | 119 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.194-285T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 4/9 | chrX | 2720071 | ||||||
| chrX:2720268
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.194-88G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 4/9 | chrX | 2720268 | ||||||
| chrX:2720319
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0072a0001c0001t0001g0073others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-37G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 4/9 | chrX | 2720319 | ||||||
| chrX:2720458
|
G | A | 45 | a0001c0001t0001g0030a0001c0001t0001g0046a0001c0001t0001g0076others(42): Show | 45 | HG00323.hp1 HG00741.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.262+34G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2720458 | ||||||
| chrX:2720620
|
C | CT | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(94): Show | 101 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.262+218dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 2720620 | |||||
| chrX:2720620
|
C | CTT | 12 | a0001c0001t0001g0092a0001c0001t0001g0104a0001c0001t0001g0133others(9): Show | 12 | HG02615.hp1 HG02615.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.262+217_262+218dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 2720620 | |||||
| chrX:2720620
|
C | CTTT | 3 | a0001c0001t0001g0172a0001c0001t0001g0175a0003c0008t0004g0087 | 3 | HG02896.hp1 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.262+216_262+218dup others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 2720620 | |||||
| chrX:2720620
|
C | CTTTT | 1 | a0001c0001t0001g0173 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.262+215_262+218dup others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 2720620 | |||||
| chrX:2720620
|
C | CTTTTT | 1 | a0001c0002t0001g0137 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.262+214_262+218dup others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 2720620 | |||||
| chrX:2720620
|
CT | C | 32 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0076others(29): Show | 32 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.262+218delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 2720620 | |||||
| chrX:2720620
|
CTT | C | 6 | a0001c0001t0001g0046a0001c0001t0001g0078a0001c0001t0002g0098others(3): Show | 6 | HG01891.hp1 HG01891.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.262+217_262+218del others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 2720620 | |||||
| chrX:2720621
|
T | TG | 1 | a0001c0001t0001g0205 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.262+197_262+198ins others(1): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2720621 | ||||||
| chrX:2720777
|
G | A | 71 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0030others(68): Show | 74 | HG00323.hp1 HG00741.hp1 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.262+353G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2720777 | ||||||
| chrX:2720786
|
G | A | 1 | a0001c0002t0001g0029 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.262+362G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2720786 | ||||||
| chrX:2720986
|
T | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(154): Show | 161 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.262+562T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2720986 | ||||||
| chrX:2721067
|
C | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0038others(5): Show | 8 | HG02451.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.262+643C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2721067 | ||||||
| chrX:2721119
|
G | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0038others(5): Show | 8 | HG02451.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.262+695G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2721119 | ||||||
| chrX:2721137
|
G | GT | 1 | a0001c0001t0001g0182 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.262+725dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 2721137 | |||||
| chrX:2721137
|
GT | G | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.262+725delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 2721137 | |||||
| chrX:2721230
|
A | T | 1 | a0001c0002t0001g0109 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.262+806A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2721230 | ||||||
| chrX:2721286
|
T | G | 2 | a0001c0001t0002g0085a0001c0001t0002g0086 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.262+862T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2721286 | ||||||
| chrX:2721374
|
C | T | 2 | a0001c0001t0001g0108a0003c0008t0004g0089 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.262+950C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2721374 | ||||||
| chrX:2721391
|
G | A | 5 | a0001c0001t0001g0092a0001c0001t0001g0192a0001c0001t0002g0033others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.262+967G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2721391 | ||||||
| chrX:2721577
|
C | T | 1 | a0001c0001t0002g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.263-1050C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2721577 | ||||||
| chrX:2721683
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.263-944A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2721683 | ||||||
| chrX:2721876
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.263-751G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2721876 | ||||||
| chrX:2722130
|
T | TA | 1 | a0001c0001t0001g0090 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.263-485dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 2722130 | |||||
| chrX:2722130
|
TA | T | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.263-485delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 2722130 | |||||
| chrX:2722139
|
AAAAC | A | 3 | a0001c0001t0001g0170a0001c0004t0001g0149a0001c0011t0001g0202 | 3 | HG02257.hp2 HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.263-483_263-480del others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 2722139 | |||||
| chrX:2722148
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263-479C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2722148 | ||||||
| chrX:2722498
|
C | G | 1 | a0001c0002t0001g0166 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.263-129C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2722498 | ||||||
| chrX:2722537
|
C | CG | 1 | a0001c0002t0001g0137 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.263-88dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 2722537 | |||||
| chrX:2722545
|
A | C | 1 | a0001c0002t0001g0008 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.263-82A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 5/9 | chrX | 2722545 | ||||||
| chrX:2722739
|
A | G | 5 | a0001c0001t0001g0092a0001c0001t0001g0192a0001c0001t0002g0033others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.310+65A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2722739 | ||||||
| chrX:2722794
|
G | A | 1 | a0001c0001t0001g0067 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.310+120G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2722794 | ||||||
| chrX:2722810
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.310+136C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2722810 | ||||||
| chrX:2722869
|
C | T | 6 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0169others(3): Show | 6 | HG00099.hp2 HG00735.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.310+195C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2722869 | ||||||
| chrX:2722876
|
C | T | 1 | a0001c0006t0001g0055 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.310+202C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2722876 | ||||||
| chrX:2722968
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.310+294G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2722968 | ||||||
| chrX:2722988
|
A | G | 15 | a0001c0001t0001g0030a0001c0001t0001g0076a0001c0001t0001g0077others(12): Show | 15 | HG00741.hp1 HG01169.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.310+314A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2722988 | ||||||
| chrX:2722988
|
A | T | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.310+314A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2722988 | ||||||
| chrX:2723015
|
T | A | 1 | a0001c0002t0001g0019 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.311-299T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2723015 | ||||||
| chrX:2723025
|
T | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.311-289T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2723025 | ||||||
| chrX:2723161
|
A | C | 51 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0046others(48): Show | 52 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.311-153A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2723161 | ||||||
| chrX:2723211
|
C | T | 2 | a0001c0001t0001g0108a0003c0008t0004g0089 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.311-103C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2723211 | ||||||
| chrX:2723245
|
A | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0072a0001c0001t0001g0073others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.311-69A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2723245 | ||||||
| chrX:2723279
|
A | C | 11 | a0001c0001t0001g0030a0001c0001t0001g0076a0001c0001t0001g0077others(8): Show | 11 | HG01884.hp1 HG02818.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.311-35A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 6/9 | chrX | 2723279 | ||||||
| chrX:2723402
|
C | T | 1 | a0001c0002t0001g0027 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.361+38C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2723402 | ||||||
| chrX:2723412
|
A | C | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0003c0008t0004g0087others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+48A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2723412 | ||||||
| chrX:2723465
|
C | T | 2 | a0001c0001t0001g0175a0001c0001t0002g0101 | 2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.361+101C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2723465 | ||||||
| chrX:2723532
|
T | TC | 83 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(80): Show | 86 | HG00639.hp2 HG00733.hp2 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.361+173dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2723532 | |||||
| chrX:2723532
|
T | TCC | 1 | a0001c0002t0001g0139 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.361+172_361+173dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2723532 | |||||
| chrX:2723561
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.361+197G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2723561 | ||||||
| chrX:2723571
|
C | T | 21 | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0056others(18): Show | 24 | HG01981.hp2 HG01993.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.361+207C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2723571 | ||||||
| chrX:2723621
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0005g0093 | 2 | HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.361+257G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2723621 | ||||||
| chrX:2723635
|
G | A | 20 | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0056others(17): Show | 23 | HG01981.hp2 HG01993.hp2 HG02165.hp1 others(20): Show |
intron_variant | MODIFIER | c.361+271G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2723635 | ||||||
| chrX:2723666
|
C | T | 1 | a0001c0002t0002g0025 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.361+302C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2723666 | ||||||
| chrX:2723781
|
C | G | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0003c0008t0004g0087others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+417C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2723781 | ||||||
| chrX:2724037
|
G | GGGAAGGA others(530): Show |
14 | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0056others(11): Show | 15 | HG01981.hp2 HG01993.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.361+674_361+675ins others(537): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2724037 | |||||
| chrX:2724037
|
G | GGGAAGGA others(582): Show |
6 | a0001c0001t0001g0030a0001c0001t0001g0076a0001c0001t0001g0077others(3): Show | 6 | HG02818.hp1 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.361+674_361+675ins others(589): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2724037 | |||||
| chrX:2724150
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0072a0001c0001t0001g0073others(7): Show | 10 | HG01070.hp1 HG01071.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.361+786A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724150 | ||||||
| chrX:2724164
|
TA | T | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.361+806delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2724164 | |||||
| chrX:2724228
|
A | G | 20 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0053others(17): Show | 21 | HG01981.hp2 HG01993.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.361+864A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724228 | ||||||
| chrX:2724361
|
G | C | 16 | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0056others(13): Show | 17 | HG01981.hp2 HG01993.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.361+997G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724361 | ||||||
| chrX:2724525
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 85 | HG00639.hp2 HG00733.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.361+1161C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724525 | ||||||
| chrX:2724566
|
C | T | 32 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(29): Show | 33 | HG01891.hp1 HG01981.hp2 HG01993.hp2 others(30): Show |
intron_variant | MODIFIER | c.361+1202C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724566 | ||||||
| chrX:2724605
|
C | CA | 1 | a0001c0001t0001g0133 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.361+1247dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2724605 | |||||
| chrX:2724653
|
CT | C | 1 | a0003c0008t0004g0071 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.361+1290delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724653 | ||||||
| chrX:2724766
|
G | A | 6 | a0001c0001t0001g0030a0001c0001t0001g0076a0001c0001t0001g0077others(3): Show | 6 | HG02818.hp1 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.361+1402G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724766 | ||||||
| chrX:2724771
|
C | G | 83 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(80): Show | 84 | HG00639.hp2 HG00733.hp2 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.361+1407C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724771 | ||||||
| chrX:2724897
|
C | CA | 21 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0053others(18): Show | 22 | HG00735.hp2 HG01993.hp2 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.362-1348dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2724897 | |||||
| chrX:2724897
|
C | CAA | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0030others(15): Show | 18 | HG01891.hp1 HG01981.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.362-1349_362-1348d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2724897 | |||||
| chrX:2724897
|
CA | C | 1 | a0003c0009t0001g0190 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.362-1348delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2724897 | |||||
| chrX:2724918
|
C | A | 1 | a0001c0002t0001g0123 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.362-1342C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724918 | ||||||
| chrX:2724918
|
CA | C | 13 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0070others(10): Show | 13 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(10): Show |
intron_variant | MODIFIER | c.362-1341delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724918 | ||||||
| chrX:2724991
|
C | T | 1 | a0001c0001t0006g0196 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.362-1269C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2724991 | ||||||
| chrX:2725050
|
A | G | 34 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0061others(31): Show | 35 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.362-1210A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725050 | ||||||
| chrX:2725067
|
C | CA | 2 | a0001c0002t0001g0008a0001c0002t0001g0213 | 2 | HG02523.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.362-1183dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2725067 | |||||
| chrX:2725098
|
T | TA | 17 | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0056others(14): Show | 18 | HG01981.hp2 HG01993.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.362-1147dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2725098 | |||||
| chrX:2725098
|
TA | T | 11 | a0001c0001t0001g0030a0001c0001t0001g0062a0001c0001t0001g0076others(8): Show | 11 | HG02818.hp1 HG02886.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.362-1147delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2725098 | |||||
| chrX:2725142
|
TC | T | 1 | a0001c0001t0001g0060 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.362-1115delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2725142 | |||||
| chrX:2725244
|
A | G | 1 | a0001c0001t0002g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.362-1016A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725244 | ||||||
| chrX:2725330
|
T | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(79): Show | 83 | HG00639.hp2 HG00733.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.362-930T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725330 | ||||||
| chrX:2725409
|
CAATAAT | C | 1 | a0001c0001t0002g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.362-844_362-839del others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2725409 | |||||
| chrX:2725444
|
A | G | 34 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(31): Show | 35 | HG01891.hp1 HG01981.hp2 HG01993.hp2 others(32): Show |
intron_variant | MODIFIER | c.362-816A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725444 | ||||||
| chrX:2725468
|
C | G | 4 | a0001c0001t0001g0092a0001c0001t0001g0192a0001c0001t0005g0034others(1): Show | 4 | HG02896.hp2 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.362-792C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725468 | ||||||
| chrX:2725612
|
TTTTTGTT others(3): Show |
T | 15 | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0056others(12): Show | 16 | HG01981.hp2 HG01993.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.362-637_362-628del others(10): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 2725612 | |||||
| chrX:2725652
|
C | T | 13 | a0001c0004t0001g0015a0001c0004t0001g0142a0001c0004t0001g0143others(10): Show | 13 | HG01168.hp1 HG01168.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.362-608C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725652 | ||||||
| chrX:2725715
|
G | A | 3 | a0001c0001t0001g0092a0001c0001t0001g0192a0001c0001t0005g0034 | 3 | HG02976.hp1 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.362-545G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725715 | ||||||
| chrX:2725734
|
C | T | 34 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(31): Show | 35 | HG01891.hp1 HG01981.hp2 HG01993.hp2 others(32): Show |
intron_variant | MODIFIER | c.362-526C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725734 | ||||||
| chrX:2725878
|
G | C | 17 | a0001c0004t0001g0015a0001c0004t0001g0142a0001c0004t0001g0143others(14): Show | 17 | HG01168.hp1 HG01168.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.362-382G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725878 | ||||||
| chrX:2725964
|
G | A | 8 | a0001c0001t0001g0030a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG02723.hp1 HG02818.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-296G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725964 | ||||||
| chrX:2725985
|
C | T | 1 | a0002c0003t0001g0203 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.362-275C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2725985 | ||||||
| chrX:2726060
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.362-200G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2726060 | ||||||
| chrX:2726251
|
C | T | 1 | a0002c0003t0001g0203 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.362-9C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 7/9 | chrX | 2726251 | ||||||
| chrX:2726475
|
G | T | 26 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0038others(23): Show | 26 | HG00639.hp2 HG00733.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.475+102G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726475 | ||||||
| chrX:2726690
|
AGCC | A | 27 | a0001c0001t0001g0011a0001c0001t0001g0092a0001c0001t0001g0192others(24): Show | 28 | HG00733.hp1 HG01168.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.475+320_475+322del others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2726690 | |||||
| chrX:2726693
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.475+320C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726693 | ||||||
| chrX:2726760
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.475+387T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726760 | ||||||
| chrX:2726769
|
G | C | 1 | a0001c0002t0001g0120 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.475+396G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726769 | ||||||
| chrX:2726826
|
T | TCAG | 51 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(48): Show | 51 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(48): Show |
intron_variant | MODIFIER | c.475+453_475+454ins others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726826 | ||||||
| chrX:2726894
|
G | A | 10 | a0001c0001t0001g0014a0001c0001t0001g0044a0001c0001t0001g0053others(7): Show | 10 | HG02080.hp2 HG02165.hp1 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.475+521G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726894 | ||||||
| chrX:2726928
|
G | A | 10 | a0001c0001t0001g0014a0001c0001t0001g0044a0001c0001t0001g0053others(7): Show | 10 | HG02080.hp2 HG02165.hp1 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.475+555G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726928 | ||||||
| chrX:2726933
|
C | T | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0003c0008t0004g0087others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.475+560C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726933 | ||||||
| chrX:2726964
|
C | T | 6 | a0001c0001t0001g0030a0001c0001t0001g0076a0001c0001t0001g0077others(3): Show | 6 | HG02818.hp1 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.475+591C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726964 | ||||||
| chrX:2726981
|
C | CA | 1 | a0001c0002t0001g0117 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.475+614dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2726981 | |||||
| chrX:2726998
|
A | G | 50 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(47): Show | 50 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(47): Show |
intron_variant | MODIFIER | c.475+625A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2726998 | ||||||
| chrX:2727019
|
C | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0072a0001c0001t0001g0073others(11): Show | 14 | HG01070.hp1 HG01071.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.475+646C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2727019 | ||||||
| chrX:2727061
|
T | C | 1 | a0001c0001t0001g0056 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.475+688T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2727061 | ||||||
| chrX:2727069
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.475+696A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2727069 | ||||||
| chrX:2727131
|
C | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0204a0001c0001t0002g0101 | 3 | HG02723.hp1 HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.475+758C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2727131 | ||||||
| chrX:2727257
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.475+884A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2727257 | ||||||
| chrX:2727325
|
G | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(143): Show | 148 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.475+952G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2727325 | ||||||
| chrX:2727417
|
TC | T | 1 | a0001c0002t0001g0124 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.475+1047delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2727417 | |||||
| chrX:2727464
|
C | T | 10 | a0001c0001t0001g0014a0001c0001t0001g0044a0001c0001t0001g0053others(7): Show | 10 | HG02080.hp2 HG02165.hp1 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.475+1091C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2727464 | ||||||
| chrX:2727537
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0072a0001c0001t0001g0073others(7): Show | 10 | HG01070.hp1 HG01071.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.475+1164C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2727537 | ||||||
| chrX:2727633
|
C | T | 2 | a0001c0001t0001g0175a0001c0001t0002g0101 | 2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.475+1260C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2727633 | ||||||
| chrX:2728111
|
G | A | 2 | a0001c0001t0002g0085a0001c0001t0002g0086 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.475+1738G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728111 | ||||||
| chrX:2728158
|
T | TACCTGGT others(1): Show |
10 | a0001c0001t0001g0014a0001c0001t0001g0044a0001c0001t0001g0053others(7): Show | 10 | HG02080.hp2 HG02165.hp1 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.475+1786_475+1793d others(10): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728158 | |||||
| chrX:2728200
|
C | CT | 12 | a0001c0001t0001g0011a0001c0001t0001g0083a0001c0001t0001g0108others(9): Show | 12 | HG00733.hp1 HG01346.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.475+1849dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728200 | |||||
| chrX:2728200
|
C | CTT | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0038others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.475+1848_475+1849d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728200 | |||||
| chrX:2728200
|
CT | C | 19 | a0001c0001t0001g0004a0001c0001t0001g0059a0001c0001t0001g0072others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.475+1849delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728200 | |||||
| chrX:2728200
|
CTTT | C | 9 | a0001c0001t0001g0044a0001c0001t0001g0053a0001c0001t0001g0056others(6): Show | 9 | HG02080.hp2 HG02165.hp1 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.475+1847_475+1849d others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728200 | |||||
| chrX:2728200
|
CTTTT | C | 1 | a0001c0001t0001g0014 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.475+1846_475+1849d others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728200 | |||||
| chrX:2728205
|
T | TC | 3 | a0001c0001t0001g0066a0001c0001t0011g0176a0001c0002t0001g0166 | 3 | HG03704.hp1 HG03927.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.475+1832_475+1833i others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728205 | ||||||
| chrX:2728206
|
T | C | 46 | a0001c0001t0001g0009a0001c0001t0001g0049a0001c0001t0001g0050others(43): Show | 48 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.475+1833T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728206 | ||||||
| chrX:2728207
|
T | C | 1 | a0001c0002t0003g0113 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.475+1834T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728207 | ||||||
| chrX:2728270
|
T | A | 1 | a0001c0001t0006g0196 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.475+1897T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728270 | ||||||
| chrX:2728392
|
C | T | 20 | a0001c0001t0001g0011a0001c0001t0001g0169a0001c0004t0001g0015others(17): Show | 21 | HG00733.hp1 HG01168.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.475+2019C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728392 | ||||||
| chrX:2728416
|
G | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0038others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.475+2043G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728416 | ||||||
| chrX:2728485
|
C | T | 5 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0021others(2): Show | 5 | HG01346.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.475+2112C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728485 | ||||||
| chrX:2728486
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.475+2113G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728486 | ||||||
| chrX:2728577
|
C | T | 1 | a0002c0003t0001g0203 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.475+2204C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728577 | ||||||
| chrX:2728625
|
C | T | 1 | a0001c0002t0001g0045 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.475+2252C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728625 | ||||||
| chrX:2728780
|
G | A | 1 | a0001c0002t0001g0019 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.475+2407G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728780 | ||||||
| chrX:2728834
|
C | CT | 27 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0044others(24): Show | 27 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.475+2481dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728834 | |||||
| chrX:2728834
|
C | CTT | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0038others(10): Show | 13 | HG01346.hp1 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.475+2480_475+2481d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728834 | |||||
| chrX:2728834
|
C | CTTT | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.475+2479_475+2481d others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728834 | |||||
| chrX:2728834
|
C | CTTTT | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.475+2478_475+2481d others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728834 | |||||
| chrX:2728834
|
CT | C | 33 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0076others(30): Show | 34 | HG00733.hp1 HG01168.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.475+2481delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728834 | |||||
| chrX:2728834
|
CTT | C | 1 | a0001c0006t0001g0040 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.475+2480_475+2481d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728834 | |||||
| chrX:2728859
|
C | T | 1 | a0001c0002t0001g0042 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.475+2486C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728859 | ||||||
| chrX:2728916
|
A | AACCTCC | 81 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(78): Show | 82 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.475+2548_475+2549i others(8): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2728916 | |||||
| chrX:2728924
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.475+2551G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2728924 | ||||||
| chrX:2729380
|
T | C | 18 | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0056others(15): Show | 18 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.475+3007T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729380 | ||||||
| chrX:2729396
|
C | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(106): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.475+3023C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729396 | ||||||
| chrX:2729440
|
TA | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.475+3069delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2729440 | |||||
| chrX:2729453
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.475+3080A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729453 | ||||||
| chrX:2729462
|
C | T | 3 | a0001c0001t0001g0092a0001c0001t0001g0192a0001c0001t0005g0034 | 3 | HG02976.hp1 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.475+3089C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729462 | ||||||
| chrX:2729608
|
C | T | 102 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(99): Show | 105 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.475+3235C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729608 | ||||||
| chrX:2729629
|
A | T | 124 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(121): Show | 127 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.475+3256A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729629 | ||||||
| chrX:2729635
|
T | G | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0003c0008t0004g0087others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.475+3262T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729635 | ||||||
| chrX:2729732
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.475+3359G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729732 | ||||||
| chrX:2729732
|
GCC | G | 1 | a0002c0003t0001g0151 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.475+3362_475+3363d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2729732 | |||||
| chrX:2729838
|
T | C | 1 | a0001c0001t0006g0196 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.475+3465T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729838 | ||||||
| chrX:2729850
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.475+3477T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729850 | ||||||
| chrX:2729989
|
C | G | 2 | a0001c0004t0002g0082a0001c0011t0001g0202 | 2 | HG01884.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.475+3616C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2729989 | ||||||
| chrX:2730014
|
C | T | 9 | a0001c0001t0001g0084a0001c0001t0001g0107a0001c0001t0001g0157others(6): Show | 9 | HG00741.hp1 HG01081.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.475+3641C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730014 | ||||||
| chrX:2730023
|
G | A | 1 | a0002c0003t0001g0203 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.475+3650G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730023 | ||||||
| chrX:2730054
|
C | T | 153 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(150): Show | 154 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.475+3681C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730054 | ||||||
| chrX:2730144
|
A | G | 1 | a0001c0002t0001g0008 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.475+3771A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730144 | ||||||
| chrX:2730175
|
C | CT | 1 | a0001c0002t0001g0141 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.475+3817dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730175 | |||||
| chrX:2730175
|
CT | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0026others(93): Show | 97 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.475+3817delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730175 | |||||
| chrX:2730175
|
CTT | C | 77 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(74): Show | 78 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.475+3816_475+3817d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730175 | |||||
| chrX:2730266
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0072a0001c0001t0001g0073others(7): Show | 10 | HG01070.hp1 HG01071.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.475+3893G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730266 | ||||||
| chrX:2730277
|
ACT | A | 23 | a0001c0001t0001g0014a0001c0001t0001g0044a0001c0001t0001g0051others(20): Show | 23 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.475+3908_475+3909d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730277 | |||||
| chrX:2730339
|
A | AT | 34 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0044others(31): Show | 34 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.475+3971dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730339 | |||||
| chrX:2730362
|
C | T | 2 | a0001c0001t0002g0085a0001c0001t0002g0086 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.475+3989C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730362 | ||||||
| chrX:2730406
|
T | C | 1 | a0001c0001t0002g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.475+4033T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730406 | ||||||
| chrX:2730461
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.475+4088C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730461 | ||||||
| chrX:2730490
|
A | T | 1 | a0001c0001t0001g0056 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.475+4117A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730490 | ||||||
| chrX:2730547
|
A | C | 17 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0172others(14): Show | 17 | HG01891.hp2 HG02630.hp2 HG02723.hp2 others(14): Show |
intron_variant | MODIFIER | c.475+4174A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730547 | ||||||
| chrX:2730575
|
ATATTTTC | A | 1 | a0001c0002t0001g0139 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.475+4206_475+4212d others(9): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730575 | |||||
| chrX:2730604
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.475+4231C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730604 | ||||||
| chrX:2730750
|
G | GA | 1 | a0001c0002t0001g0139 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.475+4380dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730750 | |||||
| chrX:2730830
|
C | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0063a0001c0002t0001g0017others(6): Show | 10 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.475+4457C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730830 | ||||||
| chrX:2730929
|
C | CA | 10 | a0001c0001t0001g0080a0001c0001t0001g0095a0001c0001t0001g0107others(7): Show | 10 | HG01081.hp1 HG01169.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.475+4575dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730929 | |||||
| chrX:2730929
|
C | CAA | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0038others(7): Show | 10 | HG00741.hp1 HG01516.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.475+4574_475+4575d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730929 | |||||
| chrX:2730929
|
CA | C | 83 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0026others(80): Show | 83 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.475+4575delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730929 | |||||
| chrX:2730929
|
CAA | C | 36 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0105others(33): Show | 37 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.475+4574_475+4575d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730929 | |||||
| chrX:2730946
|
AAAGAG | A | 1 | a0001c0001t0001g0059 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.475+4576_475+4580d others(7): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2730946 | |||||
| chrX:2730953
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.475+4580A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2730953 | ||||||
| chrX:2731016
|
C | T | 50 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0044others(47): Show | 50 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.475+4643C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731016 | ||||||
| chrX:2731221
|
C | A | 1 | a0001c0001t0001g0069 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.475+4848C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731221 | ||||||
| chrX:2731325
|
T | C | 23 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(20): Show | 23 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.475+4952T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731325 | ||||||
| chrX:2731327
|
C | T | 20 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(17): Show | 20 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.475+4954C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731327 | ||||||
| chrX:2731361
|
G | A | 9 | a0001c0001t0001g0084a0001c0001t0001g0107a0001c0001t0001g0157others(6): Show | 9 | HG00741.hp1 HG01081.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.475+4988G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731361 | ||||||
| chrX:2731375
|
A | AG | 1 | a0001c0002t0001g0139 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.475+5004dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2731375 | |||||
| chrX:2731444
|
G | A | 1 | a0002c0007t0001g0112 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.475+5071G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731444 | ||||||
| chrX:2731475
|
A | G | 4 | a0002c0003t0001g0003a0002c0003t0001g0151a0002c0003t0001g0208others(1): Show | 5 | HG01981.hp2 HG01993.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.475+5102A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731475 | ||||||
| chrX:2731547
|
C | T | 2 | a0001c0004t0002g0082a0001c0011t0001g0202 | 2 | HG01884.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.475+5174C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731547 | ||||||
| chrX:2731561
|
C | G | 1 | a0001c0001t0001g0217 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.475+5188C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731561 | ||||||
| chrX:2731612
|
A | AAC | 1 | a0001c0002t0001g0139 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.475+5239_475+5240i others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731612 | ||||||
| chrX:2731612
|
A | T | 118 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(115): Show | 119 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.475+5239A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731612 | ||||||
| chrX:2731754
|
C | T | 3 | a0001c0001t0002g0101a0001c0004t0002g0082a0001c0011t0001g0202 | 3 | HG01884.hp1 HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.475+5381C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731754 | ||||||
| chrX:2731791
|
C | T | 107 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0031others(104): Show | 108 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.475+5418C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731791 | ||||||
| chrX:2731820
|
C | CT | 1 | a0001c0002t0001g0139 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.475+5450dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2731820 | |||||
| chrX:2731883
|
T | TC | 1 | a0001c0002t0001g0139 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.475+5511dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2731883 | |||||
| chrX:2731920
|
G | C | 22 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(19): Show | 22 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.475+5547G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2731920 | ||||||
| chrX:2731970
|
T | TA | 54 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0032others(51): Show | 54 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.475+5610dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2731970 | |||||
| chrX:2731970
|
T | TAA | 20 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0075others(17): Show | 20 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.475+5609_475+5610d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2731970 | |||||
| chrX:2731970
|
T | TAAA | 1 | a0001c0001t0001g0074 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.475+5608_475+5610d others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2731970 | |||||
| chrX:2732080
|
A | G | 15 | a0001c0001t0001g0004a0001c0001t0001g0078a0001c0001t0001g0084others(12): Show | 15 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.475+5707A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732080 | ||||||
| chrX:2732155
|
T | TG | 1 | a0001c0002t0001g0139 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.475+5783dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732155 | |||||
| chrX:2732183
|
A | C | 1 | a0001c0001t0006g0220 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.475+5810A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732183 | ||||||
| chrX:2732197
|
A | C | 3 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0004t0001g0146 | 3 | HG01257.hp1 HG01346.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.475+5824A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732197 | ||||||
| chrX:2732213
|
T | TG | 1 | a0001c0002t0001g0139 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.475+5841dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732213 | |||||
| chrX:2732242
|
C | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0031others(52): Show | 55 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.475+5869C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732242 | ||||||
| chrX:2732259
|
A | AC | 1 | a0001c0002t0001g0139 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.475+5888dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732259 | |||||
| chrX:2732269
|
A | G | 192 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(189): Show | 195 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.475+5896A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732269 | ||||||
| chrX:2732298
|
C | G | 3 | a0001c0001t0001g0083a0001c0001t0001g0108a0001c0001t0006g0196 | 3 | HG01891.hp1 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.476-5902C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732298 | ||||||
| chrX:2732442
|
C | T | 1 | a0001c0002t0001g0166 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.476-5758C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732442 | ||||||
| chrX:2732487
|
CT | C | 1 | a0001c0002t0001g0139 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.476-5710delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732487 | |||||
| chrX:2732506
|
C | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0038others(5): Show | 8 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.476-5694C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732506 | ||||||
| chrX:2732523
|
T | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(84): Show | 90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.476-5677T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732523 | ||||||
| chrX:2732555
|
A | C | 1 | a0001c0002t0001g0041 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.476-5645A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732555 | ||||||
| chrX:2732562
|
C | CCT | 52 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0049others(49): Show | 53 | HG00733.hp1 HG01168.hp1 HG01168.hp2 others(50): Show |
intron_variant | MODIFIER | c.476-5627_476-5626d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732562 | |||||
| chrX:2732562
|
CCTCT | C | 1 | a0001c0001t0001g0189 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.476-5629_476-5626d others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732562 | |||||
| chrX:2732571
|
C | CTT | 16 | a0001c0001t0001g0002a0001c0001t0001g0063a0001c0001t0001g0172others(13): Show | 17 | HG00099.hp1 HG00323.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.476-5628_476-5627i others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732571 | |||||
| chrX:2732571
|
C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0072others(22): Show | 25 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.476-5629C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732571 | ||||||
| chrX:2732619
|
CCTT | C | 27 | a0001c0001t0001g0014a0001c0001t0001g0051a0001c0001t0001g0053others(24): Show | 29 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.476-5574_476-5572d others(5): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732619 | |||||
| chrX:2732675
|
T | C | 1 | a0001c0002t0001g0139 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.476-5525T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732675 | ||||||
| chrX:2732676
|
C | T | 1 | a0001c0002t0001g0139 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.476-5524C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732676 | ||||||
| chrX:2732683
|
C | CT | 1 | a0001c0002t0001g0139 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.476-5516dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732683 | |||||
| chrX:2732690
|
CT | C | 1 | a0001c0002t0001g0139 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.476-5508delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732690 | |||||
| chrX:2732721
|
T | TCTTTCCT others(60): Show |
15 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0072others(12): Show | 15 | HG01884.hp2 HG02257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.476-5457_476-5391d others(69): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732721 | |||||
| chrX:2732768
|
T | TC | 15 | a0001c0001t0001g0002a0001c0001t0001g0063a0001c0001t0001g0095others(12): Show | 16 | HG00099.hp1 HG00323.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.476-5428dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732768 | |||||
| chrX:2732773
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0038others(5): Show | 8 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.476-5427T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732773 | ||||||
| chrX:2732801
|
CCTTT | C | 3 | a0001c0002t0001g0117a0001c0002t0001g0150a0001c0002t0001g0154 | 3 | HG02165.hp2 NA19084.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.476-5394_476-5391d others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732801 | |||||
| chrX:2732851
|
G | T | 153 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(150): Show | 157 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.476-5349G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732851 | ||||||
| chrX:2732869
|
T | C | 1 | a0001c0002t0001g0041 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.476-5331T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732869 | ||||||
| chrX:2732902
|
CTTCTTTC others(6): Show |
C | 1 | a0001c0001t0001g0217 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.476-5296_476-5284d others(15): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2732902 | |||||
| chrX:2732938
|
T | C | 1 | a0001c0002t0002g0025 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.476-5262T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2732938 | ||||||
| chrX:2733051
|
G | GT | 1 | a0001c0001t0001g0200 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.476-5147dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2733051 | |||||
| chrX:2733059
|
C | CCT | 47 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(44): Show | 48 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.476-5138_476-5137d others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2733059 | |||||
| chrX:2733072
|
T | C | 1 | a0001c0004t0001g0149 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.476-5128T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733072 | ||||||
| chrX:2733085
|
C | T | 40 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(37): Show | 41 | HG00099.hp1 HG00323.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.476-5115C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733085 | ||||||
| chrX:2733149
|
CTCTG | C | 35 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(32): Show | 36 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.476-5047_476-5044d others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2733149 | |||||
| chrX:2733223
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0038others(5): Show | 8 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.476-4977T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733223 | ||||||
| chrX:2733336
|
G | T | 3 | a0001c0001t0006g0220a0001c0004t0001g0149a0003c0008t0004g0071 | 3 | HG02818.hp2 NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.476-4864G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733336 | ||||||
| chrX:2733476
|
C | G | 1 | a0002c0007t0001g0028 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.476-4724C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733476 | ||||||
| chrX:2733484
|
G | A | 1 | a0003c0008t0004g0071 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.476-4716G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733484 | ||||||
| chrX:2733497
|
C | T | 1 | a0002c0007t0001g0028 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.476-4703C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733497 | ||||||
| chrX:2733525
|
C | T | 18 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 19 | HG00099.hp1 HG01071.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.476-4675C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733525 | ||||||
| chrX:2733688
|
T | G | 2 | a0001c0001t0001g0108a0001c0001t0006g0220 | 2 | HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.476-4512T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733688 | ||||||
| chrX:2733706
|
T | G | 2 | a0001c0001t0001g0217a0003c0008t0004g0071 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.476-4494T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733706 | ||||||
| chrX:2733798
|
G | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0031others(7): Show | 10 | HG00099.hp2 HG00735.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.476-4402G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733798 | ||||||
| chrX:2733846
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0006g0220 | 2 | HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.476-4354T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733846 | ||||||
| chrX:2733850
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0006g0220 | 2 | HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.476-4350C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733850 | ||||||
| chrX:2733887
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0006g0220 | 2 | HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.476-4313A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733887 | ||||||
| chrX:2733922
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.476-4278A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733922 | ||||||
| chrX:2733961
|
G | A | 4 | a0001c0001t0001g0108a0001c0001t0006g0220a0002c0003t0001g0151others(1): Show | 4 | HG01981.hp2 HG01993.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-4239G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2733961 | ||||||
| chrX:2734065
|
C | T | 4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 4 | HG02630.hp1 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.476-4135C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2734065 | ||||||
| chrX:2734168
|
A | AT | 1 | a0001c0006t0001g0201 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.476-4028dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2734168 | |||||
| chrX:2734205
|
TTTTC | T | 2 | a0002c0003t0001g0005a0002c0003t0001g0203 | 2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.476-3987_476-3984d others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2734205 | |||||
| chrX:2734374
|
T | G | 1 | a0001c0001t0006g0196 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.476-3826T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2734374 | ||||||
| chrX:2734398
|
C | G | 1 | a0001c0001t0006g0196 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.476-3802C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2734398 | ||||||
| chrX:2734538
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0006g0220 | 2 | HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.476-3662T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2734538 | ||||||
| chrX:2734620
|
CT | C | 12 | a0001c0001t0001g0108a0001c0001t0001g0178a0001c0001t0001g0182others(9): Show | 12 | HG01891.hp2 HG06807.hp1 NA18939.hp1 others(9): Show |
intron_variant | MODIFIER | c.476-3569delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2734620 | |||||
| chrX:2734704
|
CT | C | 6 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(3): Show | 6 | HG02630.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.476-3488delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2734704 | |||||
| chrX:2734729
|
C | T | 4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 4 | HG02630.hp1 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.476-3471C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2734729 | ||||||
| chrX:2734772
|
ATTTC | A | 1 | a0001c0001t0002g0185 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.476-3424_476-3421d others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2734772 | |||||
| chrX:2734776
|
CT | C | 1 | a0002c0007t0001g0112 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.476-3415delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2734776 | |||||
| chrX:2734795
|
C | CT | 2 | a0001c0001t0005g0034a0001c0001t0005g0093 | 2 | HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.476-3396dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2734795 | |||||
| chrX:2734956
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0006g0220 | 2 | HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.476-3244G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2734956 | ||||||
| chrX:2735057
|
T | A | 1 | a0001c0001t0001g0059 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.476-3143T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735057 | ||||||
| chrX:2735210
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0006g0220 | 2 | HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.476-2990C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735210 | ||||||
| chrX:2735382
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.476-2818C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735382 | ||||||
| chrX:2735390
|
G | T | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0003c0008t0004g0087others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.476-2810G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735390 | ||||||
| chrX:2735511
|
C | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(101): Show | 106 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.476-2689C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735511 | ||||||
| chrX:2735533
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.476-2667C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735533 | ||||||
| chrX:2735690
|
G | A | 5 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0183others(2): Show | 5 | HG01891.hp2 NA18941.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.476-2510G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735690 | ||||||
| chrX:2735848
|
T | C | 6 | a0001c0001t0001g0108a0001c0001t0006g0220a0002c0003t0001g0005others(3): Show | 6 | HG02004.hp2 HG02896.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.476-2352T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735848 | ||||||
| chrX:2735872
|
G | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(89): Show | 94 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.476-2328G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735872 | ||||||
| chrX:2735930
|
C | T | 3 | a0001c0001t0001g0100a0001c0002t0001g0125a0001c0002t0001g0127 | 3 | HG01123.hp1 HG01123.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.476-2270C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735930 | ||||||
| chrX:2735985
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.476-2215G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2735985 | ||||||
| chrX:2736018
|
T | C | 8 | a0001c0001t0001g0091a0001c0001t0001g0175a0001c0001t0002g0085others(5): Show | 8 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.476-2182T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736018 | ||||||
| chrX:2736058
|
T | C | 8 | a0001c0001t0001g0091a0001c0001t0001g0175a0001c0001t0002g0085others(5): Show | 8 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.476-2142T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736058 | ||||||
| chrX:2736150
|
C | T | 2 | a0001c0001t0005g0034a0001c0001t0005g0093 | 2 | HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.476-2050C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736150 | ||||||
| chrX:2736159
|
G | A | 2 | a0001c0001t0001g0091a0001c0011t0001g0202 | 2 | HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.476-2041G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736159 | ||||||
| chrX:2736167
|
G | A | 1 | a0001c0002t0001g0043 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.476-2033G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736167 | ||||||
| chrX:2736168
|
T | C | 1 | a0001c0002t0001g0043 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.476-2032T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736168 | ||||||
| chrX:2736196
|
T | C | 1 | a0001c0002t0001g0043 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.476-2004T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736196 | ||||||
| chrX:2736201
|
C | CA | 3 | a0001c0001t0001g0060a0001c0001t0009g0064a0002c0007t0001g0112 | 3 | HG02257.hp1 NA18974.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.476-1983dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2736201 | |||||
| chrX:2736201
|
CA | C | 17 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(14): Show | 17 | HG01891.hp2 HG02004.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.476-1983delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2736201 | |||||
| chrX:2736214
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.476-1986A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736214 | ||||||
| chrX:2736214
|
AAAAG | A | 2 | a0001c0001t0001g0108a0001c0001t0006g0220 | 2 | HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.476-1982_476-1979d others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2736214 | |||||
| chrX:2736239
|
G | A | 1 | a0001c0002t0001g0137 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.476-1961G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736239 | ||||||
| chrX:2736247
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0009g0064 | 2 | HG00733.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.476-1953A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736247 | ||||||
| chrX:2736257
|
C | T | 1 | a0003c0008t0004g0071 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.476-1943C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736257 | ||||||
| chrX:2736332
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.476-1868C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736332 | ||||||
| chrX:2736355
|
CTTCT | C | 2 | a0001c0001t0001g0063a0001c0002t0001g0047 | 2 | HG00099.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.476-1844_476-1841d others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736355 | ||||||
| chrX:2736419
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(82): Show | 87 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.476-1781A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736419 | ||||||
| chrX:2736427
|
A | G | 18 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(15): Show | 18 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.476-1773A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736427 | ||||||
| chrX:2736459
|
T | G | 1 | a0001c0001t0006g0196 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.476-1741T>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736459 | ||||||
| chrX:2736534
|
G | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0038others(5): Show | 8 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.476-1666G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736534 | ||||||
| chrX:2736610
|
T | C | 1 | a0001c0002t0001g0008 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.476-1590T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736610 | ||||||
| chrX:2736623
|
C | T | 1 | a0001c0002t0001g0027 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.476-1577C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736623 | ||||||
| chrX:2736786
|
G | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(28): Show | 32 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.476-1414G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736786 | ||||||
| chrX:2736812
|
G | A | 1 | a0001c0002t0002g0167 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.476-1388G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736812 | ||||||
| chrX:2736813
|
C | T | 6 | a0001c0001t0001g0217a0001c0001t0006g0220a0001c0002t0001g0021others(3): Show | 6 | HG01175.hp1 HG01346.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.476-1387C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736813 | ||||||
| chrX:2736816
|
C | T | 1 | a0001c0001t0006g0220 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.476-1384C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736816 | ||||||
| chrX:2736834
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.476-1366G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736834 | ||||||
| chrX:2736873
|
T | TAATA | 18 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(15): Show | 18 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.476-1303_476-1300d others(6): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2736873 | |||||
| chrX:2736873
|
TAATAAAT others(1): Show |
T | 1 | a0001c0001t0012g0207 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.476-1307_476-1300d others(10): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2736873 | |||||
| chrX:2736884
|
TAAATAAA | T | 7 | a0001c0001t0001g0217a0001c0001t0006g0220a0001c0002t0001g0021others(4): Show | 7 | HG01175.hp1 HG01346.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.476-1315_476-1309d others(9): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736884 | ||||||
| chrX:2736968
|
T | C | 7 | a0001c0001t0001g0217a0001c0001t0006g0220a0001c0002t0001g0021others(4): Show | 7 | HG01175.hp1 HG01346.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.476-1232T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736968 | ||||||
| chrX:2736999
|
C | G | 3 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0101 | 3 | HG01070.hp1 HG01071.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.476-1201C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2736999 | ||||||
| chrX:2737091
|
T | C | 218 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(215): Show | 222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.476-1109T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737091 | ||||||
| chrX:2737119
|
C | T | 1 | a0003c0008t0004g0071 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.476-1081C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737119 | ||||||
| chrX:2737166
|
T | C | 4 | a0001c0001t0001g0217a0001c0001t0006g0220a0004c0012t0007g0013others(1): Show | 4 | HG01516.hp2 HG02109.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-1034T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737166 | ||||||
| chrX:2737204
|
G | A | 3 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0101 | 3 | HG01070.hp1 HG01071.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.476-996G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737204 | ||||||
| chrX:2737241
|
G | C | 2 | a0001c0001t0002g0033a0001c0001t0002g0098 | 2 | HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.476-959G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737241 | ||||||
| chrX:2737282
|
A | T | 11 | a0002c0003t0001g0003a0002c0003t0001g0099a0002c0003t0001g0151others(8): Show | 12 | HG01496.hp1 HG01981.hp2 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.476-918A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737282 | ||||||
| chrX:2737291
|
T | C | 4 | a0001c0001t0001g0217a0001c0001t0006g0220a0004c0012t0007g0013others(1): Show | 4 | HG01516.hp2 HG02109.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-909T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737291 | ||||||
| chrX:2737310
|
G | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(104): Show | 109 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.476-890G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737310 | ||||||
| chrX:2737322
|
T | C | 2 | a0004c0012t0007g0013a0004c0015t0007g0018 | 2 | HG01516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.476-878T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737322 | ||||||
| chrX:2737325
|
A | C | 2 | a0004c0012t0007g0013a0004c0015t0007g0018 | 2 | HG01516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.476-875A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737325 | ||||||
| chrX:2737334
|
C | T | 2 | a0004c0012t0007g0013a0004c0015t0007g0018 | 2 | HG01516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.476-866C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737334 | ||||||
| chrX:2737422
|
C | T | 4 | a0001c0001t0001g0217a0001c0001t0006g0220a0004c0012t0007g0013others(1): Show | 4 | HG01516.hp2 HG02109.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-778C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737422 | ||||||
| chrX:2737426
|
T | TG | 223 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(220): Show | 227 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.476-772dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2737426 | |||||
| chrX:2737504
|
AT | A | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.476-691delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2737504 | |||||
| chrX:2737564
|
G | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(100): Show | 105 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.476-636G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737564 | ||||||
| chrX:2737613
|
GC | G | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.476-585delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2737613 | |||||
| chrX:2737617
|
C | A | 66 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(63): Show | 67 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.476-583C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737617 | ||||||
| chrX:2737619
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.476-581C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737619 | ||||||
| chrX:2737662
|
C | G | 4 | a0001c0001t0001g0217a0001c0001t0006g0220a0004c0012t0007g0013others(1): Show | 4 | HG01516.hp2 HG02109.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-538C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737662 | ||||||
| chrX:2737702
|
G | A | 3 | a0001c0001t0001g0051a0001c0001t0001g0133a0003c0008t0004g0071 | 3 | HG00438.hp1 NA18906.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.476-498G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2737702 | ||||||
| chrX:2737863
|
C | CT | 3 | a0001c0001t0001g0182a0001c0001t0002g0156a0001c0004t0001g0142 | 3 | HG02273.hp1 HG03669.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.476-324dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2737863 | |||||
| chrX:2737962
|
AT | A | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.476-236delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2737962 | |||||
| chrX:2738046
|
A | T | 1 | a0001c0002t0001g0128 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.476-154A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2738046 | ||||||
| chrX:2738063
|
CG | C | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.476-133delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 2738063 | |||||
| chrX:2738134
|
GT | G | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.476-65delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2738134 | ||||||
| chrX:2738139
|
T | C | 4 | a0001c0001t0001g0217a0001c0001t0006g0220a0004c0012t0007g0013others(1): Show | 4 | HG01516.hp2 HG02109.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-61T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 8/9 | chrX | 2738139 | ||||||
| chrX:2738274
|
C | T | 5 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(2): Show | 5 | HG02630.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.532+18C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2738274 | ||||||
| chrX:2738288
|
C | T | 1 | a0001c0001t0001g0002 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.532+32C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2738288 | ||||||
| chrX:2738300
|
TC | T | 1 | a0001c0001t0001g0059 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.532+47delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2738300 | |||||
| chrX:2738324
|
TC | T | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.532+71delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2738324 | |||||
| chrX:2738394
|
G | A | 9 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(6): Show | 9 | HG01516.hp2 HG02109.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.532+138G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2738394 | ||||||
| chrX:2738404
|
AG | A | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.532+151delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2738404 | |||||
| chrX:2738512
|
TCC | T | 1 | a0001c0001t0003g0152 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.532+258_532+259del others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2738512 | |||||
| chrX:2738559
|
G | C | 7 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(4): Show | 7 | HG02109.hp2 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.532+303G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2738559 | ||||||
| chrX:2738680
|
G | A | 5 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(2): Show | 5 | HG02630.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.532+424G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2738680 | ||||||
| chrX:2738809
|
C | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(106): Show | 111 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.532+553C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2738809 | ||||||
| chrX:2738849
|
C | CT | 1 | a0001c0001t0001g0080 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.532+602dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2738849 | |||||
| chrX:2738849
|
CT | C | 1 | a0001c0001t0011g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.532+602delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2738849 | |||||
| chrX:2738969
|
TC | T | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.532+715delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2738969 | |||||
| chrX:2738992
|
C | CT | 1 | a0001c0001t0011g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.532+736_532+737ins others(1): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2738992 | ||||||
| chrX:2739003
|
G | A | 8 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.532+747G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739003 | ||||||
| chrX:2739018
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.532+762G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739018 | ||||||
| chrX:2739035
|
A | AT | 1 | a0001c0001t0011g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.532+783dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739035 | |||||
| chrX:2739115
|
G | A | 1 | a0001c0002t0001g0037 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.532+859G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739115 | ||||||
| chrX:2739125
|
TC | T | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.532+872delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739125 | |||||
| chrX:2739132
|
G | C | 2 | a0001c0001t0006g0196a0001c0001t0006g0220 | 2 | HG01891.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.532+876G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739132 | ||||||
| chrX:2739195
|
A | C | 10 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(7): Show | 10 | HG01516.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.532+939A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739195 | ||||||
| chrX:2739298
|
G | GA | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.532+1049dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739298 | |||||
| chrX:2739313
|
G | T | 10 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(7): Show | 10 | HG01516.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.532+1057G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739313 | ||||||
| chrX:2739337
|
A | AT | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.532+1085dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739337 | |||||
| chrX:2739337
|
A | C | 10 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(7): Show | 10 | HG01516.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.532+1081A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739337 | ||||||
| chrX:2739410
|
CA | C | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.532+1157delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739410 | |||||
| chrX:2739445
|
A | G | 10 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(7): Show | 10 | HG01516.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.532+1189A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739445 | ||||||
| chrX:2739449
|
T | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0076a0001c0001t0001g0077others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.532+1193T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739449 | ||||||
| chrX:2739460
|
T | A | 10 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(7): Show | 10 | HG01516.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.532+1204T>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739460 | ||||||
| chrX:2739462
|
CT | C | 1 | a0002c0007t0001g0112 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.532+1211delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739462 | |||||
| chrX:2739514
|
AC | A | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.532+1260delC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739514 | |||||
| chrX:2739568
|
G | GC | 1 | a0001c0001t0011g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.533-1209dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739568 | |||||
| chrX:2739612
|
A | G | 1 | a0001c0004t0002g0082 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.533-1167A>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739612 | ||||||
| chrX:2739614
|
TA | T | 2 | a0001c0001t0011g0176a0006c0013t0008g0012 | 2 | NA18992.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.533-1163delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739614 | |||||
| chrX:2739691
|
T | TG | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.533-1087dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739691 | |||||
| chrX:2739749
|
TG | T | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.533-1028delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739749 | |||||
| chrX:2739800
|
A | AG | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.533-979_533-978ins others(1): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739800 | ||||||
| chrX:2739802
|
G | T | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.533-977G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739802 | ||||||
| chrX:2739816
|
C | G | 61 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(58): Show | 63 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.533-963C>G | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739816 | ||||||
| chrX:2739822
|
T | TC | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.533-954dupC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739822 | |||||
| chrX:2739843
|
A | AG | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.533-934dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739843 | |||||
| chrX:2739920
|
T | TA | 33 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0038others(30): Show | 33 | HG01070.hp1 HG01071.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.533-837dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739920 | |||||
| chrX:2739920
|
T | TAA | 16 | a0001c0001t0001g0108a0002c0003t0001g0003a0002c0003t0001g0099others(13): Show | 17 | HG00639.hp1 HG01496.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.533-838_533-837dup others(2): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739920 | |||||
| chrX:2739920
|
T | TAAA | 4 | a0001c0001t0001g0204a0002c0003t0001g0005a0002c0007t0001g0022others(1): Show | 4 | HG02004.hp2 HG02809.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.533-839_533-837dup others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739920 | |||||
| chrX:2739920
|
T | TAAAA | 7 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.533-840_533-837dup others(4): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739920 | |||||
| chrX:2739920
|
TA | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0056others(5): Show | 9 | HG01257.hp1 HG01516.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.533-837delA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739920 | |||||
| chrX:2739961
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.533-818G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2739961 | ||||||
| chrX:2739997
|
CAGG | C | 1 | a0001c0001t0001g0217 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.533-779_533-777del others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2739997 | |||||
| chrX:2740008
|
CT | C | 1 | a0001c0014t0001g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.533-769delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2740008 | |||||
| chrX:2740095
|
AAAT | A | 32 | a0001c0001t0001g0108a0001c0001t0002g0033a0001c0001t0002g0085others(29): Show | 33 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.533-666_533-664del others(3): Show |
CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2740095 | |||||
| chrX:2740109
|
A | C | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.533-670A>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740109 | ||||||
| chrX:2740187
|
G | C | 1 | a0001c0004t0001g0015 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.533-592G>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740187 | ||||||
| chrX:2740192
|
A | T | 1 | a0001c0001t0001g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.533-587A>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740192 | ||||||
| chrX:2740255
|
T | TA | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.533-523dupA | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2740255 | |||||
| chrX:2740258
|
G | A | 42 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(39): Show | 43 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.533-521G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740258 | ||||||
| chrX:2740275
|
G | T | 42 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(39): Show | 43 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.533-504G>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740275 | ||||||
| chrX:2740397
|
CT | C | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.533-380delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2740397 | |||||
| chrX:2740463
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG00735.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.533-316C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740463 | ||||||
| chrX:2740464
|
AT | A | 1 | a0001c0001t0011g0176 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.533-312delT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2740464 | |||||
| chrX:2740523
|
C | T | 3 | a0001c0001t0005g0034a0001c0001t0005g0093a0001c0001t0005g0223 | 3 | HG02976.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.533-256C>T | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740523 | ||||||
| chrX:2740579
|
A | AT | 15 | a0001c0001t0002g0033a0001c0001t0002g0085a0001c0001t0002g0086others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.533-192dupT | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2740579 | |||||
| chrX:2740657
|
G | A | 10 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0183others(7): Show | 10 | HG01257.hp2 HG01517.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.533-122G>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740657 | ||||||
| chrX:2740728
|
T | TC | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.533-51_533-50insC | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740728 | ||||||
| chrX:2740737
|
A | AG | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.533-39dupG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2740737 | |||||
| chrX:2740742
|
C | A | 15 | a0001c0001t0002g0033a0001c0001t0002g0085a0001c0001t0002g0086others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.533-37C>A | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740742 | ||||||
| chrX:2740744
|
TG | T | 1 | a0006c0013t0008g0012 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.533-32delG | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chrX | 2740744 | |||||
| chrX:2740756
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.533-23T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740756 | ||||||
| chrX:2740759
|
T | C | 15 | a0001c0001t0002g0033a0001c0001t0002g0085a0001c0001t0002g0086others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.533-20T>C | CD99 | ENSG00000002586.20 | transcript | ENST00000381192.10 | protein_coding | 9/9 | chrX | 2740759 |